| Primary | Number of Participants Who Agree or Completely Agree (a Score of 4 or Higher) Across All Items on the Feasibility of Intervention Measure (FIM) | Feasibility of Intervention Measure (FIM) were employed to evaluate the feasibility of CABENUVA administration at Infusion Centers (IC)/ alternate sites of administration (ASA). Higher scores on FIM indicate greater feasibility, where each item can be scored from 1 to 5: Completely disagree (score=1), disagree (score=2), neither agree or disagree (score=3), agree (score=4), completely agree (score=5). This scoring looked at the number responding '4' or '5' to each question divided by the number completing all 4-items where "items" refer to the individual questions or statements that participants respond to in order to assess their perceptions of an intervention. Each item is designed to measure a specific aspect of either acceptability or feasibility. | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| | | Title | Denominators | Categories |
|---|
| | |
| |
| Secondary | Number of Participants Who Agree or Completely Agree (a Score of 4 or Higher) Across All Items on the FIM at Month 1 and 3 | | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Months 1 and 3 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| | |
| Secondary | Number of HIV Care Providers Who Agree or Completely Agree (a Score of 4 or Higher) Across All Items on the FIM at Month 1, 4 and 8 | | Analysis was performed on the HIV care providers which includes any HIV care provider who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Months 1, 4, and 8 | | | | ID | Title | Description |
|---|
| OG000 | HIV Care Providers | Eligible HIV Care Providers completed study assessments at each data collection time point. |
| | |
| Secondary | Number of IC/ ASA Staff Who Agree or Completely Agree (a Score of 4 or Higher) Across All Items on the FIM Prior to Month 1 and at Months 3 and 8 | | Analysis was performed on the IC/ASA staff which includes any IC/ASA staff who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | Prior to Month 1 (Baseline) and at Months 3 and 8 | | | | ID | Title | Description |
|---|
| OG000 | IC/ASA Staff | Eligible IC/ASA Staff completed study assessments at each data collection time point. |
| | |
| Secondary | Change in FIM Score Over Time in Participants at Month 3 and 8 | The mean score for feasibility of the intervention administration was calculated by averaging the responses from the 4 items. The responses were scored based on a scale of 1 to 5 where 1=completely disagree, 2=disagree, 3=neither agree nor disagree, 4=agree, and 5=completely agree. | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Mean | Standard Deviation | Scores on a scale | | From Month 1 (Baseline) to Months 3 and 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| |
| Secondary | Change in FIM Score Over Time in HIV Care Providers at Month 4 and 8 | | Analysis was performed on the HIV care providers which includes any HIV care provider who completed any portion of any questionnaire at the specified timepoint. | Posted | | Mean | Standard Deviation | Scores on a scale | | From Month 1 (Baseline) to Months 4 and 8 | | | | ID | Title | Description |
|---|
| OG000 | HIV Care Providers | Eligible HIV care providers completed study assessments at each data collection time point. |
| | |
| Secondary | Change in FIM Score Over Time in IC/ ASA Staff at Month 3 and 8 | | Analysis was performed on the IC/ASA staff which includes any IC/ASA staff who completed any portion of any questionnaire at the specified timepoint. | Posted | | Mean | Standard Deviation | Scores on a scale | | From Month 1 (Baseline) to Months 3 and 8 | | | | ID | Title | Description |
|---|
| OG000 | IC/ASA Staff | Eligible IC/ASA Staff completed study assessments at each data collection time point. |
| | |
| Secondary | Number of Participants Assessed for Feasibility of CABENUVA Administration by Other Quantitative Questionnaires at Month 1 | The tailored questionnaire for participants receiving CABENUVA was developed specifically for this study and contains items regarding the reasons for switching to CABENUVA, adherence to their previous oral HIV medication, preferences and attitudes regarding their medication regimen, and perceived advantages and disadvantages of receiving injections at the IC/ASA. In this outcome measure, participants were asked about their views on the IC/ASA administration model (any/biggest concerns about receiving CABENUVA at an infusion center). | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 1 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| |
| Secondary | Number of Participants Assessed for Feasibility of CABENUVA Administration (Concern About Continuing to Receive CABENUVA) by Other Quantitative Questionnaires at Month 3 and 8 | The tailored questionnaire for participants receiving CABENUVA was developed specifically for this study and contains items regarding the reasons for switching to CABENUVA, adherence to their previous oral HIV medication, preferences and attitudes regarding their medication regimen, and perceived advantages and disadvantages of receiving injections at the IC/ASA. In this outcome measure, participants were asked about their views on the IC/ASA administration model (any concerns about continuing to receive CABENUVA at an infusion center) at Months 3 and 8. | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 3 and 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| |
| Secondary | Number of Participants Assessed for Feasibility of CABENUVA Administration by Other Quantitative Questionnaires at Month 3 and 8 | Participants were asked about their views on the IC/ASA administration model (biggest concerns about continuing to receive CABENUVA at an infusion center). | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 3 and 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| |
| Secondary | Number of HIV Care Providers Assessed for Feasibility of CABENUVA Administration in Participants by Other Quantitative Questionnaires at Month 1 | The tailored HIV care provider/clinical staff questionnaire was developed specifically for this study and contains items regarding the provider's practice and experience, as well as their attitudes, expectations, and concerns regarding the use of CABENUVA/long-acting injectable administered by ICs/ASAs. | Analysis was performed on the HIV care providers which includes any HIV care provider who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 1 | | | | ID | Title | Description |
|---|
| OG000 | HIV Care Providers | Eligible HIV care Providers completed study assessments at each data collection time point. |
| |
| Secondary | Number of HIV Care Providers Assessed for Feasibility of CABENUVA Administration in Participants by Other Quantitative Questionnaires at Month 4 | | Analysis was performed on the HIV care providers which includes any HIV care provider who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 4 | | | | ID | Title | Description |
|---|
| OG000 | HIV Care Providers | Eligible HIV Care Providers completed study assessments at each data collection time point. |
| | |
| Secondary | Number of HIV Care Providers Assessed for Feasibility of CABENUVA Administration in Participants by Other Quantitative Questionnaires at Month 8 | | Analysis was performed on the HIV care providers which includes any HIV care provider who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 8 | | | | ID | Title | Description |
|---|
| OG000 | HIV Care Providers | Eligible HIV Care Providers completed study assessments at each data collection time point. |
| | |
| Secondary | Number of IC/ASA Staff Assessed for Feasibility of CABENUVA Administration in Participants by Other Quantitative Questionnaires Prior to Month 1 | The tailored IC staff questionnaire was developed specifically for this study and contains items regarding the staff member's role at the IC, as well as their attitudes, concerns, and anticipated/implemented procedures regarding the use of CABENUVA/long-acting injectable administered by ICs. The IC/ASA staff members were asked to indicate their level of concern across 16 areas of potential concern, on a five-point scale from "not at all concerned" to "extremely concerned." | Analysis was performed on the IC/ASA staff which includes any IC/ASA staff who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | Prior to Month 1 (Baseline) | | | | ID | Title | Description |
|---|
| OG000 | IC/ASA Staff | Eligible IC/ASA Staff completed study assessments at each data collection time point. |
| |
| Secondary | Number of IC/ASA Staff Assessed for Feasibility of CABENUVA Administration in Participants Assessed by Other Quantitative Questionnaires at Month 3 | The IC/ASA staff members were asked to indicate their level of concern across 16 areas of potential concern, on a five-point scale from "not at all concerned" to "extremely concerned." | Analysis was performed on the IC/ASA staff which includes any IC/ASA staff who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 3 | | | | ID | Title | Description |
|---|
| OG000 | IC/ASA Staff | Eligible IC/ASA Staff completed study assessments at each data collection time point. |
| |
| Secondary | Number of IC/ASA Staff Assessed for Feasibility of CABENUVA Administration in Participants by Other Quantitative Questionnaires at Month 8 | The IC/ASA staff members were asked to indicate their level of concern across 16 areas of potential concern, on a five-point scale from "not at all concerned" to "extremely concerned." | Analysis was performed on the IC/ASA staff which includes any IC/ASA staff who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 8 | | | | ID | Title | Description |
|---|
| OG000 | IC/ASA Staff | Eligible IC/ASA Staff completed study assessments at each data collection time point. |
| |
| Secondary | Number of Participants Assessed for Feasibility of CABENUVA Administration by Qualitative Interviews at Month 8 | Qualitative interviews were conducted at Month 8 to evaluate the opinions of participants on the feasibility of CABENUVA administration at IC/ASA. | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| |
| Secondary | Number of HIV Care Providers Assessed for Feasibility of CABENUVA Administration in Participants by Qualitative Interviews at Month 8 | Qualitative interviews were conducted at Month 8 to evaluate the general opinion of HIV care providers on the feasibility of referring participants to receive CABENUVA at the IC/ASA. | Analysis was performed on the HIV care providers which includes any HIV care provider who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 8 | | | | ID | Title | Description |
|---|
| OG000 | HIV/Care Providers | Eligible HIV Care Providers completed study assessments at each data collection time point. |
| |
| Secondary | Number of IC/ASA Staff Assessed for Feasibility of CABENUVA Administration in Participants by Qualitative Interviews at Month 8 | Qualitative interviews were conducted at Month 8 to evaluate the general opinion of IC/ ASA staff on feasibility of CABENUVA administration at the IC/ASA. | Analysis was performed on the IC/ASA staff which includes any IC/ASA staff who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 8 | | | | ID | Title | Description |
|---|
| OG000 | IC/ASA Staff | Eligible IC/ASA Staff completed study assessments at each data collection time point. |
| |
| Secondary | Composite Score of Feasibility Process Indications | Composite score of feasibility process was calculated as the mean of the following four scores: FIM Score, Consent Rate, Show Rate, and Return Rate at Visit, on a 0 to 100 scale, where higher numbers correspond to better feasibility. | Data was collected at the clinic level and analysis was performed on the Clinics that consented one or more participants for administration of intervention. | Posted | | Mean | Standard Deviation | Scores on a scale | | Up to and including Month 8 | Clinics | Clinics | | ID | Title | Description |
|---|
| OG000 | Clinics | Eligible clinics that consented one or more participants for injection were considered in this arm to evaluate feasibility. |
| |
| Secondary | Change in Composite Score and Each Item of Composite Score Over Time | This outcome measure was planned to evaluate change in composite score from baseline to month 8 according to the protocol. The composite score was however not evaluated as a change over time but as a point in time at month 8 as the components of each of the feasibility composite score (FIM score, consent rate, show rate and return rate) were captured at different time intervals. | Data was collected at the clinic level and analysis was performed on the Clinics that consented one or more participants for administration of intervention. | Posted | | Mean | Standard Deviation | Scores on a scale | | Baseline (Month 1) and at Month 8 | Clinics | Clinics | | ID | Title | Description |
|---|
| OG000 | Clinics | Eligible clinics that consented one or more participants for injection were considered in this arm to evaluate feasibility. |
| |
| Secondary | Number of HIV Care Providers Who Agree or Completely Agree (a Score of 4 or Higher) Across All Items on the Acceptability of Intervention Measure (AIM) | AIM was employed to evaluate the acceptability of CABENUVA administration at Infusion Centers/ ASAs. Higher scores for AIM indicate greater acceptability, where each item was scored from 1 to 5: Completely disagree (score=1), disagree (score=2), neither agree or disagree (score=3), agree (score=4), completely agree (score=5). | Analysis was performed on the HIV care providers which includes any HIV care provider who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | Months 1 (Baseline), 4, and 8 | | | | ID | Title | Description |
|---|
| OG000 | HIV Care Providers | Eligible HIV Care Providers completed study assessments at each data collection time point. |
| |
| Secondary | Number of Participants Who Agree or Completely Agree (a Score of 4 or Higher) Across All Items on the AIM | AIM were employed to evaluate the acceptability of CABENUVA administration at Infusion Centers/ ASAs. Higher scores for AIM indicate greater acceptability, where each item was scored from 1 to 5: Completely disagree (score=1), disagree (score=2), neither agree or disagree (score=3), agree (score=4), completely agree (score=5). | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | Month 1 (Baseline), 3 and 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| |
| Secondary | Number of IC/ ASA Staff Who Agree or Completely Agree (a Score of 4 or Higher) Across All Items on the AIM | AIM were employed to evaluate the acceptability of CABENUVA administration at Infusion Centers/ ASAs. Higher scores for AIM indicate greater acceptability, where each item was scored from 1 to 5: Completely disagree (score=1), disagree (score=2), neither agree or disagree (score=3), agree (score=4), completely agree (score=5). | Analysis was performed on the IC/ASA staff which includes any IC/ASA staff who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | Prior to Month 1 (Baseline), and at Month 3 and 8 | | | | ID | Title | Description |
|---|
| OG000 | IC/ASA Staff | Eligible IC/ASA Staff completed study assessments at each data collection time point. |
| |
| Secondary | Change in AIM Score Over Time in HIV Care Providers at Month 4 and 8 | The mean score for acceptability of the intervention is calculated by averaging the responses from 4 items. The responses were scored based on a scale of 1 to 5 where 1=completely disagree, 2=disagree, 3=neither agree nor disagree, 4=agree, and 5=completely agree. | Analysis was performed on the HIV care providers which includes any HIV care provider who completed any portion of any questionnaire at the specified timepoint. | Posted | | Mean | Standard Deviation | Scores on a scale | | Month 1 (Baseline), at Months 4 and 8 | | | | ID | Title | Description |
|---|
| OG000 | HIV Care Providers | Eligible HIV Care Providers completed study assessments at each data collection time point. |
| |
| Secondary | Change in AIM Score Over Time in Participants at Month 3 and 8 | The mean score for acceptability of the intervention is calculated by averaging the responses from 4 items. The responses were scored based on a scale of 1 to 5 where 1=completely disagree, 2=disagree, 3=neither agree nor disagree, 4=agree, and 5=completely agree. | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Mean | Standard Deviation | Scores on a scale | | Month 1 (Baseline), at Months 3 and 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| |
| Secondary | Change in AIM Score Over Time in IC/ ASA Staff at Month 3 and 8 | The mean score for acceptability of the intervention is calculated by averaging the responses from 4 items. The responses were scored based on a scale of 1 to 5 where 1=completely disagree, 2=disagree, 3=neither agree nor disagree, 4=agree, and 5=completely agree. | Analysis was performed on the IC/ASA staff which includes any IC/ASA staff who completed any portion of any questionnaire at the specified timepoint. | Posted | | Mean | Standard Deviation | Scores on a scale | | Month 1 (Baseline), at Months 3 and 8 | | | | ID | Title | Description |
|---|
| OG000 | IC/ASA Staff | Eligible IC/ASA Staff completed study assessments at each data collection time point. |
| |
| Secondary | Number of HIV Care Providers Assessed for Acceptability of CABENUVA Administration in Participants at IC/ ASA by Other Quantitative Questionnaire at Months 1, 4 and 8 | | Analysis was performed on the HIV care providers which includes any HIV care provider who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Months 1, 4 and 8 | | | | ID | Title | Description |
|---|
| OG000 | HIV Care Providers | Eligible HIV Care Providers completed study assessments at each data collection time point. |
| | |
| Secondary | Number of Participants Assessed for Acceptability of CABENUVA Administration at IC/ ASA by Other Quantitative Questionnaire in at Months 1, 3 and 8 | The participants were asked how acceptable it was to come to the IC/ASA for CABENUVA using a 7-point scale from "very acceptable" to "very unacceptable" where 1= very acceptable, 2= somewhat acceptable, 3= a little acceptable, 4= neutral, 5= a little unacceptable, 6= somewhat unacceptable and 7= very unacceptable. | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Months 1, 3 and 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| |
| Secondary | Number of IC/ ASA Staff Assessed for Acceptability of CABENUVA Administration in Participants at IC/ ASA by Other Quantitative Questionnaire Prior to Month 1 | | Analysis was performed on the IC/ASA staff which includes any IC/ASA staff who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | Prior to Month 1 (Baseline) | | | | ID | Title | Description |
|---|
| OG000 | IC/ASA Staff | Eligible IC/ASA Staff completed study assessments at each data collection time point. |
| | |
| Secondary | Number of IC/ ASA Staff Assessed for Acceptability of CABENUVA Administration in Participants at IC/ ASA by Other Quantitative Questionnaire at Months 3 and 8 | | Analysis was performed on the IC/ASA staff which includes any IC/ASA staff who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Months 3 and 8 | | | | ID | Title | Description |
|---|
| OG000 | IC/ASA Staff | Eligible IC/ASA Staff completed study assessments at each data collection time point. |
| | |
| Secondary | Number of Participants Assessed for Acceptability of CABENUVA Administration at IC/ASA by Qualitative Interviews at Month 8 | Participants were asked about their opinion on acceptability of CABENUVA administration at the IC/ASA. | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible IC/ASA Staff completed study assessments at each data collection time point. |
| |
| Secondary | Number of HIV Care Providers Assessed for Acceptability of CABENUVA Administration in Participants at IC/ASA by Qualitative Interviews at Month 8 | HIV care providers were asked about their opinion on the acceptability of participants receiving CABENUVA at the IC/ASA. | Analysis was performed on the HIV care providers which includes any HIV care provider who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 8 | | | | ID | Title | Description |
|---|
| OG000 | HIV Care Providers | Eligible HIV Care Providers completed study assessments at each data collection time point. |
| |
| Secondary | Number of IC/ASA Staff Assessed for Acceptability of CABENUVA Administration in Participants at IC/ASA by Qualitative Interviews at Month 8 | IC/ASA staff were asked about their opinion on the acceptability of administering CABENUVA at an IC/ASA. | Analysis was performed on the IC/ASA staff which includes any IC/ASA staff who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 8 | | | | ID | Title | Description |
|---|
| OG000 | IC/ASA Staff | Eligible IC/ASA Staff completed study assessments at each data collection time point. |
| |
| Secondary | Number of Expert Panel That Agree or Completely Agree (a Score of 4 or Higher) Across All Items on the FIM Scale | | Analysis was performed on the Expert Panel which includes any Expert Panel member who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | Prior to Month 1 (Baseline), and at Month 3 and 6 | | | | ID | Title | Description |
|---|
| OG000 | Expert Panel | Pre-determined Expert Panel comprising of selected HIV care providers and key IC staff completed study assessments at each data collection time point. |
| |
| Secondary | Number of Expert Panel That Agree or Completely Agree (a Score of 4 or Higher) Across All Items on the AIM Scale | | Analysis was performed on the Expert Panel which includes any Expert Panel member who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | Prior to Month 1 (Baseline), and at Month 3 and 6 | | | | ID | Title | Description |
|---|
| OG000 | Expert Panel | Pre-determined Expert Panel comprising of selected HIV care providers and key IC staff completed study assessments at each data collection time point. |
| |
| Secondary | Change in FIM Score of Expert Panel Over Time Through Month 6 | | Analysis was performed on the Expert Panel which includes any Expert Panel member who completed any portion of any questionnaire at the specified timepoint. | Posted | | Mean | Standard Deviation | Scores on a scale | | Prior to Month 1 (Baseline) and Up to Month 6 | | | | ID | Title | Description |
|---|
| OG000 | Expert Panel | Pre-determined Expert Panel comprising of selected HIV care providers and key IC staff completed study assessments at each data collection time point. |
| | |
| Secondary | Change in AIM Score of Expert Panel Over Time Through Month 6 | | Analysis was performed on the Expert Panel which includes any Expert Panel member who completed any portion of any questionnaire at the specified timepoint. | Posted | | Mean | Standard Deviation | Scores on a scale | | Prior to Month 1 (Baseline) and Up to Month 6 | | | | ID | Title | Description |
|---|
| OG000 | Expert Panel | Pre-determined Expert Panel comprising of selected HIV care providers and key IC staff completed study assessments at each data collection time point. |
| | |
| Secondary | Number of Expert Panel Members Assessed for Feasibility, Acceptability and Process of Insurance Coverage for CABENUVA Administration in Participants by Quantitative Questionnaires Prior to Month 1 | | Analysis was performed on the Expert Panel which includes any Expert Panel member who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | Prior to Month 1 (Baseline) | | | | ID | Title | Description |
|---|
| OG000 | Expert Panel | Pre-determined Expert Panel comprising of selected HIV care providers and key IC staff completed study assessments at each data collection time point. |
| |
| Secondary | Number of Expert Panel Members Assessed for Feasibility, Acceptability and Process of Communication for CABENUVA Administration in Participants by Quantitative Questionnaires Prior to Month 1 | | Analysis was performed on the Expert Panel which includes any Expert Panel member who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | Prior to Month 1 (Baseline) | | | | ID | Title | Description |
|---|
| OG000 | Expert Panel | Pre-determined Expert Panel comprising of selected HIV care providers and key IC staff completed study assessments at each data collection time point. |
| |
| Secondary | Number of Expert Panel Members Assessed for Feasibility, Acceptability and Process of CABENUVA Administration (Interval of Time) in Participants by Quantitative Questionnaires Prior to Month 1 | In this outcome measure, Expert Panel members were asked about their views on the IC/ASA administration model (for patients receiving CABENUVA injections at the infusion center, what is the preferred interval of time for patients to be seen by their HIV provider). | Analysis was performed on the Expert Panel which includes any Expert Panel member who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | Prior to Month 1 (Baseline) | | | | ID | Title | Description |
|---|
| OG000 | Expert Panel | Pre-determined Expert Panel comprising of selected HIV care providers and key IC staff completed study assessments at each data collection time point. |
| |
| Secondary | Number of Expert Panel Members Assessed for Feasibility, Acceptability and Process of Referring Participants for CABENUVA Administration by Quantitative Questionnaires Prior to Month 1 | | Analysis was performed on the Expert Panel which includes any Expert Panel member who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | Prior to Month 1 (Baseline) | | | | ID | Title | Description |
|---|
| OG000 | Expert Panel | Pre-determined Expert Panel comprising of selected HIV care providers and key IC staff completed study assessments at each data collection time point. |
| |
| Secondary | Number of Expert Panel Members Assessed for Feasibility, Acceptability and Process of Insurance and Communication for CABENUVA Administration in Participants by Quantitative Questionnaires at Month 3 | | Analysis was performed on the Expert Panel which includes any Expert Panel member who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 3 | | | | ID | Title | Description |
|---|
| OG000 | Expert Panel | Pre-determined Expert Panel comprising of selected HIV care providers and key IC staff completed study assessments at each data collection time point. |
| |
| Secondary | Number of Expert Panel Members Assessed for Feasibility, Acceptability and Process of Insurance and Communication for CABENUVA Administration in Participants by Quantitative Questionnaires at Month 6 | | Analysis was performed on the Expert Panel which includes any Expert Panel member who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 6 | | | | ID | Title | Description |
|---|
| OG000 | Expert Panel | Pre-determined Expert Panel comprising of selected HIV care providers and key IC staff completed study assessments at each data collection time point. |
| |
| Secondary | Number of Expert Panel Members Assessed for Feasibility, Acceptability and Process of CABENUVA Administration in Participants by Qualitative Interviews Prior to Month 1 | The Expert Panel were asked about the key steps focused on the process of CABENUVA administration at IC/ASAs in order to inform the development of the blueprint. | Analysis was performed on the Expert Panel which includes any Expert Panel member who completed any portion of any questionnaire at the specified timepoint study. | Posted | | Count of Participants | | Participants | | Prior to Month 1 (Baseline) | | | | ID | Title | Description |
|---|
| OG000 | Expert Panel | Pre-determined Expert Panel comprising of selected HIV care providers and key IC staff completed study assessments at each data collection time point. |
| |
| Secondary | Number of Expert Panel Members Assessed for Feasibility, Acceptability and Process of CABENUVA Administration in Participants by Qualitative Interviews at Month 6 | The Expert Panel were asked about the key steps focused on the process of CABENUVA administration at IC/ASAs in order to inform the development of the blueprint. | Analysis was performed on the Expert Panel which includes any Expert Panel member who completed any portion of any questionnaire at the specified timepoint study. | Posted | | Count of Participants | | Participants | | At Month 6 | | | | ID | Title | Description |
|---|
| OG000 | Expert Panel | Pre-determined Expert Panel comprising of selected HIV care providers and key IC staff completed study assessments at each data collection time point. |
| |
| Secondary | Number of Participants Assessed for Perceptions, Facilitators and Barriers/Concerns of CABENUVA Administration With Other Quantitative Questionnaires at Month 1 | | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 1 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| | |
| Secondary | Number of Participants Assessed for Perceptions, Facilitators and Barriers/Concerns of CABENUVA Administration With Other Quantitative Questionnaires (Q 1) at Month 3 and 8 | | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 3 and 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| |
| Secondary | Number of Participants Assessed for Perceptions, Facilitators and Barriers/Concerns of CABENUVA Administration With Other Quantitative Questionnaires (Q 2) at Months 3 and 8 | | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Months 3 and 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| |
| Secondary | Number of Participants Assessed for Perceptions, Facilitators and Barriers/Concerns of CABENUVA Administration With Other Quantitative Questionnaires (Q 3) at Months 3 and 8 | | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Months 3 and 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| |
| Secondary | Number of Participants Assessed for Perceptions, Facilitators and Barriers/Concerns of CABENUVA Administration With Other Quantitative Questionnaires (Q 4) at Months 3 and 8 | | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Months 3 and 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| |
| Secondary | Number of Participants Assessed for Perceptions, Facilitators and Barriers/Concerns of CABENUVA Administration With Other Quantitative Questionnaires (Q 5) at Months 3 and 8 | | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Months 3 and 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| |
| Secondary | Number of Participants Assessed for Perceptions, Facilitators and Barriers/Concerns of CABENUVA Administration With Other Quantitative Questionnaires (Q 6) at Months 3 and 8 | | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Months 3 and 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| |
| Secondary | Number of Participants Assessed for Perceptions, Facilitators and Barriers/Concerns of CABENUVA Administration With Other Quantitative Questionnaires (Q 7) at Months 3 and 8 | | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Months 3 and 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| |
| Secondary | Number of Participants Assessed for Perceptions, Facilitators and Barriers/Concerns of CABENUVA Administration With Other Quantitative Questionnaires (Q 8) at Months 3 and 8 | | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Months 3 and 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| |
| Secondary | Number of Participants Assessed for Perceptions, Facilitators and Barriers/Concerns of CABENUVA Administration With Other Quantitative Questionnaires (Q 9) at Months 3 and 8 | | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Months 3 and 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| |
| Secondary | Number of Participants Assessed for Perceptions, Facilitators and Barriers/Concerns of CABENUVA Administration With Other Quantitative Questionnaires (Q 10) at Months 3 and 8 | Participants were asked their opinion on who did they reach out to obtain answers to their questions. | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Months 3 and 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| |
| Secondary | Number of Participants Assessed for Perceptions, Facilitators and Barriers/Concerns of CABENUVA Administration With Other Quantitative Questionnaires (Q 11) at Months 3 and 8 | | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Months 3 and 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| |
| Secondary | Number of IC/ASA Staff Assessed for Perceptions, Facilitators and Barriers/Concerns of CABENUVA Administration in Participants With Other Quantitative Questionnaires Prior to Month 1 | Since CABENUVA must be administered within a two-week treatment window every month, IC/ASA staff were asked their opinion about the ease or difficulty in appointment re-scheduling and implementation of CABENUVA administration in their work-flow. | Analysis was performed on the IC/ASA staff which includes any IC/ASA staff who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | Prior to Month 1 (Baseline) | | | | ID | Title | Description |
|---|
| OG000 | IC/ASA Staff | Eligible IC/ASA Staff completed study assessments at each data collection time point. |
| |
| Secondary | Number of IC/ASA Staff Assessed for Perceptions, Facilitators and Barriers/Concerns of CABENUVA Administration in Participants With Other Quantitative Questionnaires at Month 3 | Since CABENUVA must be administered within a two-week treatment window (+/-)7 days relative to the target treatment date), the IC/ASA staff was asked their opinion about the ease or difficulty in appointment scheduling and re-scheduling and implementation of CABENUVA administration in their workflow. | Analysis was performed on the IC/ASA staff which includes any IC/ASA staff who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 3 | | | | ID | Title | Description |
|---|
| OG000 | IC/ASA Staff | Eligible IC/ASA Staff completed study assessments at each data collection time point. |
| |
| Secondary | Number of IC/ASA Staff Assessed for Perceptions, Facilitators and Barriers/Concerns of CABENUVA Administration in Participants With Other Quantitative Questionnaires at Month 8 | Since CABENUVA must be administered within a two-week treatment window (+/-)7 days relative to the target treatment date), the IC/ASA staff was asked their opinion about the ease or difficulty in appointment scheduling and re-scheduling and implementation of CABENUVA administration in their workflow. | Analysis was performed on the IC/ASA staff which includes any IC/ASA staff who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 8 | | | | ID | Title | Description |
|---|
| OG000 | IC/ASA Staff | Eligible IC/ASA Staff completed study assessments at each data collection time point. |
| |
| Secondary | Number of HIV Care Providers Assessed for Perceptions, Facilitators and Barriers/Concerns of CABENUVA Administration in Participants With Quantitative Questionnaires at Month 1 | | Analysis was performed on the HIV care providers which includes any HIV care provider who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 1 | | | | ID | Title | Description |
|---|
| OG000 | HIV Care Provider | Eligible HIV Care Providers completed study assessments at each data collection time point. |
| | |
| Secondary | Number of HIV Care Providers Assessed for Perceptions, Facilitators and Barriers/Concerns of CABENUVA Administration in Participants With Quantitative Questionnaires at Month 4 | | Analysis was performed on the HIV care providers which includes any HIV care provider who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 4 | | | | ID | Title | Description |
|---|
| OG000 | HIV Care Provider | Eligible HIV Care Providers completed study assessments at each data collection time point. |
| | |
| Secondary | Number of HIV Care Providers Assessed for Perceptions, Facilitators and Barriers/Concerns of CABENUVA Administration in Participants With Quantitative Questionnaires at Month 8 | | Analysis was performed on the HIV care providers which includes any HIV care provider who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 8 | | | | ID | Title | Description |
|---|
| OG000 | HIV Care Provider | Eligible HIV Care Providers completed study assessments at each data collection time point. |
| | |
| Secondary | Number of Participants Assessed for Facilitators of CABENUVA Administration by Qualitative Interviews at Month 8 | Participants were asked about facilitators that made the process of receiving CABENUVA at IC/ASAs easier. | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| |
| Secondary | Number of IC/ASA Staff Assessed for Barriers/Concerns of CABENUVA Administration in Participants by Qualitative Interviews at Month 8 | IC/ASA staff were asked their opinion on the infrastructure impact of administering CABENUVA. | Analysis was performed on the IC/ASA staff which includes any IC/ASA staff who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 8 | | | | ID | Title | Description |
|---|
| OG000 | IC/ASA Staff | Eligible IC/ASA Staff completed study assessments at each data collection time point. |
| |
| Secondary | Number of HIV Care Providers Assessed for Perceptions, Facilitators and Barriers/Concerns of CABENUVA Administration in Participants by Qualitative Interviews at Month 8 | HIV care providers were asked about the facilitators and challenges related to referring participants to IC/ASAs. | Analysis was performed on the HIV care providers which includes any HIV care provider who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 8 | | | | ID | Title | Description |
|---|
| OG000 | HIV Care Provider | Eligible HIV Care Providers completed study assessments at each data collection time point. |
| |
| Secondary | Number of Participants Assessed for Preference on the Location to Receive CABENUVA With Other Quantitative Questionnaires at Months 1, 3 and 8 | | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 1, 3 and 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| | |
| Secondary | Number of Participants Assessed for Preference on the Location to Receive CABENUVA by Qualitative Interviews at Month 8 | | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| | |
| Secondary | Number of Participants Assessed for Advantages of Receiving CABENUVA at IC/ ASA by Other Quantitative Questionnaires at Month 1 | In this outcome measure, participants were asked about their views on the IC/ASA administration model (advantages of going to the infusion center to receive CABENUVA). | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 1 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| |
| Secondary | Number of Participants Assessed for Advantages of Receiving CABENUVA at IC/ ASA by Other Quantitative Questionnaires at Months 3 and 8 | In this outcome measure, participants were asked about their views on the IC/ASA administration model (advantages of going to the infusion center to receive CABENUVA). | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Months 3 and 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| |
| Secondary | Number of HIV Care Providers Assessed for Advantages of Referring Participants to the IC/ ASA to Receive CABENUVA by Other Quantitative Questionnaires at Month 1, 4 and 8 | In this outcome measure, HIV care providers were asked about their views on the IC/ASA administration model (advantages of referring patients to an infusion center for CABENUVA). | Analysis was performed on the HIV care providers which includes any HIV care provider who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Months 1, 4 and 8 | | | | ID | Title | Description |
|---|
| OG000 | HIV Care Providers | Eligible HIV Care Providers completed study assessments at each data collection time point. |
| |
| Secondary | Number of Participants Assessed for Advantages of Receiving CABENUVA at IC/ ASA by Qualitative Interviews at Month 8 | | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| | |
| Secondary | Number of HIV Care Providers Assessed for Advantages of Participants Receiving CABENUVA at IC/ ASA by Qualitative Interviews at Month 8 | | Analysis was performed on the HIV care providers which includes any HIV care provider who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 8 | | | | ID | Title | Description |
|---|
| OG000 | HIV Care Providers | Eligible HIV Care Providers completed study assessments at each data collection time point. |
| | |
| Secondary | Number of Participants Assessed for Disadvantages of Receiving CABENUVA at IC/ ASA by Other Quantitative Questionnaires at Month 1 | In this outcome measure, participants were asked about their views on the IC/ASA administration model (disadvantages of going to the infusion center to receive CABENUVA). | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 1 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| |
| Secondary | Number of Participants Assessed for Disadvantages of Receiving CABENUVA at IC/ ASA by Other Quantitative Questionnaires at Months 3 and 8 | In this outcome measure, participants were asked about their views on the IC/ASA administration model (disadvantages of going to the infusion center to receive CABENUVA). | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Months 3 and 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| |
| Secondary | Number of HIV Care Providers Assessed for Disadvantages of Referring Participants to the IC/ ASA to Receive CABENUVA by Other Quantitative Questionnaires at Month 1 | In this outcome measure, HIV care providers were asked about their views on the IC/ASA administration model (potential disadvantages of referring patients to an IC for CABENUVA). | Analysis was performed on the HIV care providers which includes any HIV care provider who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 1 | | | | ID | Title | Description |
|---|
| OG000 | HIV Care Providers | Eligible HIV Care Providers completed study assessments at each data collection time point. |
| |
| Secondary | Number of HIV Care Providers Assessed for Disadvantages of Referring Participants to the IC/ ASA to Receive CABENUVA by Other Quantitative Questionnaires at Months 4 and 8 | In this outcome measure, HIV care providers were asked about their views on the IC/ASA administration model (disadvantages of referring patients to an IC for CABENUVA). | Analysis was performed on the HIV care providers which includes any HIV care provider who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Months 4 and 8 | | | | ID | Title | Description |
|---|
| OG000 | HIV Care Providers | Eligible HIV Care Providers completed study assessments at each data collection time point. |
| |
| Secondary | Number of Participants Assessed for Disadvantages of Receiving CABENUVA at IC/ ASA by Qualitative Interviews at Month 8 | | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| | |
| Secondary | Number of HIV Care Providers Assessed for Disadvantages for Participants Receiving CABENUVA at IC/ ASA by Qualitative Interviews at Month 8 | In this outcome measure, HIV care providers were asked about their views on the IC/ASA administration model (disadvantages for participants receiving CABENUVA at IC/ASAs). | Analysis was performed on the HIV care providers which includes any HIV care provider who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 8 | | | | ID | Title | Description |
|---|
| OG000 | HIV Care Providers | Eligible HIV Care Providers completed study assessments at each data collection time point. |
| |
| Secondary | Number of Participants Assessed for Acceptability of the Process of Receiving Injections at ICs/ ASAs by Other Quantitative Questionnaires at Month 1 | | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 1 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| | |
| Secondary | Number of Participants Assessed for Acceptability of the Process of Receiving Injections at ICs/ ASAs by Other Quantitative Questionnaires at Month 3 | | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 3 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| | |
| Secondary | Number of Participants Assessed for Acceptability of the Process of Receiving Injections at ICs/ ASAs by Other Quantitative Questionnaires at Month 8 | | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| | |
| Secondary | Number of Participants Assessed for Acceptability of the Process of Receiving Injections at ICs/ ASAs (Time Spent at IC) by Other Quantitative Questionnaires at Months 3 and 8 | | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Months 3 and 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| |
| Secondary | Number of HIV Care Providers Assessed for Acceptability of the Process of Referring Participants to the IC/ ASA for CABENUVA by Other Quantitative Questionnaires at Months 1, 4 and 8 | HIV care providers were asked about the type of patients they found acceptable to refer to an IC to receive CABENUVA. | Analysis was performed on the HIV care providers which includes any HIV care provider who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Months 1, 4 and 8 | | | | ID | Title | Description |
|---|
| OG000 | HIV Care Providers | Eligible HIV Care Providers completed study assessments at each data collection time point. |
| |
| Secondary | Number of Participants Assessed for Acceptability of the Process of Receiving Injections at ICs/ ASAs by Qualitative Interviews at Month 8 | Participants were asked about their opinion on the acceptability of CABENUVA administration at the IC. | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| |
| Secondary | Number of HIV Care Providers Assessed for Acceptability of the Process of Participants Receiving Injections at ICs/ ASAs by Qualitative Interviews at Month 8 | | Analysis was performed on the HIV care providers which includes any HIV care provider who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 8 | | | | ID | Title | Description |
|---|
| OG000 | HIV Care Providers | Eligible HIV Care Providers completed study assessments at each data collection time point. |
| | |
| Secondary | Number of IC/ASA Staff Assessed for Usefulness of the Blueprint Intervention With Other Quantitative Questionnaires Prior to Month 1 | The blueprint guides IC/ASA staff on what to do with referrals to receive CABENUVA at the IC/ASA. | Analysis was planned to be performed on the IC/ASA staff which includes any IC/ASA staff who completed any portion of any questionnaire at the specified timepoint. Prior to Month 1 there were no referrals given; hence the blueprint was not used and therefore it was not assessed. | Posted | | | | | | Prior to Month 1 (Baseline) | | | | ID | Title | Description |
|---|
| OG000 | IC/ASA Staff | Eligible IC/ASA Staff completed study assessments at each data collection time point. |
| |
| Secondary | Number of IC/ASA Staff Assessed for Usefulness of the Blueprint Intervention With Other Quantitative Questionnaires at Month 3 and 8 | The blueprint guides IC/ASA staff on what to do with referrals to receive CABENUVA at the IC/ASA. | Analysis was performed on the IC/ASA staff which includes any IC/ASA staff who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Months 3 and 8 | | | | ID | Title | Description |
|---|
| OG000 | IC/ASA Staff | Eligible IC/ASA Staff completed study assessments at each data collection time point. |
| |
| Secondary | Number of HIV Care Providers Assessed for Usefulness of Plan of Treatment (POT) by Other Quantitative Questionnaires at Months 4 and 8 | | Analysis was performed on the HIV care providers which includes any HIV care provider who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Months 4 and 8 | | | | ID | Title | Description |
|---|
| OG000 | HIV Care Providers | Eligible HIV Care Providers completed study assessments at each data collection time point. |
| | |
| Secondary | Number of IC/ASA Staff Assessed for Usefulness of the Blueprint Intervention and POT Assessed by Qualitative Interviews at Month 8 | | Analysis was performed on the IC/ASA staff which includes any IC/ASA staff who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | Month 8 | | | | ID | Title | Description |
|---|
| OG000 | IC/ASA Staff | Eligible IC/ASA Staff completed study assessments at each data collection time point. |
| | |
| Secondary | Number of HIV Care Providers Assessed for Usefulness of the Blueprint Intervention and POT by Qualitative Interviews at Month 8 | The blueprint guides HIV care providers on what to do with referrals to receive CABENUVA at the IC/ASA. | Analysis was performed on the HIV care providers which includes any HIV care provider who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | Month 8 | | | | ID | Title | Description |
|---|
| OG000 | HIV Care Providers | Eligible HIV Care Providers completed study assessments at each data collection time point. |
| |
| Secondary | Number of IC/ASA Staff Assessed for Overall Opinion of Administering the Injection at an IC/ ASA by Other Quantitative Questionnaires Prior to Month 1 and at Months 3 and 8 | | Analysis was performed on the IC/ASA staff which includes any IC/ASA staff who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | Prior to Month 1 (Baseline) and Months 3 and 8 | | | | ID | Title | Description |
|---|
| OG000 | IC/ASA Staff | Eligible IC/ASA Staff completed study assessments at each data collection time point. |
| | |
| Secondary | Number of Participants Assessed for Overall Opinion of Receiving the Injection at an IC/ ASA by Other Quantitative Questionnaires at Months 1, 3 and 8 | | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Months 1, 3 and 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| | |
| Secondary | Number of HIV Care Providers Assessed for Overall Opinion of Referring the Participant to an IC/ ASA by Other Quantitative Questionnaires at Month 1 | | Analysis was performed on the HIV care providers which includes any HIV care provider who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 1 | | | | ID | Title | Description |
|---|
| OG000 | HIV Care Providers | Eligible HIV Care Providers completed study assessments at each data collection time point. |
| | |
| Secondary | Number of HIV Care Providers Assessed for Overall Opinion of Referring the Participant to an IC/ ASA by Other Quantitative Questionnaires at Month 4 | | Analysis was performed on the HIV care providers which includes any HIV care provider who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 4 | | | | ID | Title | Description |
|---|
| OG000 | HIV Care Providers | Eligible HIV Care Providers completed study assessments at each data collection time point. |
| | |
| Secondary | Number of HIV Care Providers Assessed for Overall Opinion of Referring the Participant to an IC/ ASA by Other Quantitative Questionnaires at Month 8 | | Analysis was performed on the HIV care providers which includes any HIV care provider who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 8 | | | | ID | Title | Description |
|---|
| OG000 | HIV Care Providers | Eligible HIV Care Providers completed study assessments at each data collection time point. |
| | |
| Secondary | Number of HIV Care Providers Assessed for Overall Opinion of Continuing to Refer Participants to an IC/ ASA by Other Quantitative Questionnaires at Month 8 | | Analysis was performed on the HIV care providers which includes any HIV care provider who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 8 | | | | ID | Title | Description |
|---|
| OG000 | HIV Care Providers | Eligible HIV Care Providers completed study assessments at each data collection time point. |
| | |
| Secondary | Number of Participants Assessed for Overall Opinion of Receiving the Injection at an IC/ ASA by Qualitative Interview at Month 8 | Participants were asked about their overall favorable and non-favorable opinion of receiving CABENUVA at the IC/ASA. | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 8 | | | | ID | Title | Description |
|---|
| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
| |
| Secondary | Number of HIV Care Providers Assessed for Overall Opinion of Referring Patients to an IC/ ASA by Qualitative Interview at Month 8 | HIV care providers were asked about their overall favoring and non-favoring opinions on referring participants to IC/ASA for CABENUVA administration. | Analysis was performed on the HIV care providers which includes any HIV care provider who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 8 | | | | ID | Title | Description |
|---|
| OG000 | HIV Care Providers | Eligible HIV Care Providers completed study assessments at each data collection time point. |
| |
| Secondary | Number of IC/ASA Staff Assessed for Overall Opinion of Administering the Injection at an IC/ ASA by Qualitative Interview at Month 8 | IC/ASA staff was asked about their overall opinion on the participants referral process. | Analysis was performed on the IC/ASA staff which includes any IC/ASA staff who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Participants | | Participants | | At Month 8 | | | | ID | Title | Description |
|---|
| OG000 | IC/ASA Staff | Eligible IC/ASA Staff completed study assessments at each data collection time point. |
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| Secondary | Number of Injections Occurring Within Target Window From Target Date | This outcome measure evaluates the fidelity to treatment and dosing window. Fidelity to treatment and dosing window was defined based on a ±7-day window from target treatment date based on the calendar date of baseline injection. | Analysis was performed on the Safety set which includes any participant who completed any portion of any questionnaire at the specified timepoint. | Posted | | Count of Units | | Injections | | Up to and including Month 8 | Injections | Injections | | ID | Title | Description |
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| OG000 | Participants Receiving CABENUVA | Eligible participants received CABENUVA injections intramuscularly at infusion centers/ASAs monthly or every-2-months. |
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