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| ID | Type | Description | Link |
|---|---|---|---|
| R21CA215557-02 | U.S. NIH Grant/Contract | View source |
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| Name | Class |
|---|---|
| National Cancer Institute (NCI) | NIH |
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Head and neck cancer survivors and their primary caregivers (N=25 dyads) will be enrolled to pilot test a nutrition support system with a care planning clinic visit and a caregiver mobile App. Participants will be asked to complete baseline and 6-week follow-up surveys. The clinic session (offered in person or remotely) will include a needs assessment and a tailored care plan with information, educational materials and referrals about participants' symptoms, behaviors, social concerns and caregiving tasks. After the visit, the program will provide an App for caregivers with follow-up resources and mobile support for one month.
The long-term goal of this research is to improve physical, emotional and social post-treatment outcomes in head and neck cancer survivors and caregivers by implementing a nutrition-focused mobile-Support program to prepare and support caregivers after treatment.
Head and neck cancer survivors and their primary caregivers (N=25 dyads) will be recruited to a single-arm intervention study to evaluate the feasibility, acceptability and short-term effects of a nutrition-focused mobile support system. The intervention includes 1) a clinic visit (offered in-person or virtually) with a tablet-based needs assessment at the end of or after completing treatment which will generate 2) a tailored care plan with messages, educational materials and referrals mapped to survivor and caregiver-endorsed concerns and 3) a caregiver App with encouragement, reminders and tips delivered through messaging and peer videos. Participants will complete baseline and 6-week follow-up surveys.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| HEART | Experimental | Patients and caregivers will complete a HEART visit virtually or in person. The visit includes a needs assessment that generates a tailored care plan with messages, referrals and educational materials for discussion with a nurse. Caregivers will receive brief training about the HEART App and then use the App for 4 weeks with bi-weekly real-time prompts and feedback. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Heart APP | Behavioral | The HEART intervention includes a care planning visit for patients and caregivers and an App for caregivers focused on nutrition, self-care and support. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Number of Participants Meeting Patient-Caregiver Session and Care Plan Acceptability Criteria | Investigator developed questionnaire investigating acceptability of session intervention and care plan. Items were rated on a 6-point descriptive scale from strongly disagree to strongly agree. Participants that meet criteria are those that chose moderately or strongly agree. Items included: Session made me feel prepared, care plan information was helpful emotionally, care plan was helpful practically, amount of information in care plan provided was appropriate, timing of session of session was appropriate. | 6 week follow-up visit |
| Intervention Delivery/ Fidelity | Number of caregivers receiving all session content and delivery of the intervention as planned (intro to session, nurse care plan discussion, viewed nutritional support video, app training). | 6 week follow up visit |
| Intervention Reach | Percentage of those recruited who completed baseline and 6 week follow up surveys and the intervention session. | Baseline and 6 week follow up visit |
| Measure | Description | Time Frame |
|---|---|---|
| Ease of Use/System Usability | System Usability Scale (SUS) - The SUS consists of a 10 item questionnaire with five response options for respondents; from Strongly agree to Strongly disagree. Scores range from 0-100, with higher scores indicating better usability. | 6 week follow up visit only (no baseline comparison) |
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Patient Inclusion Criteria:
Patient Exclusion Criteria:
Caregiver Inclusion Criteria:
Caregiver Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Katherine Sterba, PhD. MPH | Medical University of SC | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Medical University of South Carolina | Charleston | South Carolina | 29425 | United States |
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Head and neck cancer patients and caregivers were recruited at the end of radiation therapy.
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| ID | Title | Description |
|---|---|---|
| FG000 | HEART | Patients and caregivers will complete a HEART visit virtually or in person. The visit includes a needs assessment that generates a tailored care plan with messages, referrals and educational materials for discussion with a nurse. Caregivers will receive brief training about the HEART App and then use the App for 4 weeks with bi-weekly real-time prompts and feedback. Heart APP: The HEART intervention includes a care planning visit for patients and caregivers and an App for caregivers focused on nutrition, self-care and support. |
| Title | Milestones | Reasons Not Completed | ||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
|
Not provided
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| ID | Title | Description |
|---|---|---|
| BG000 | HEART | Patients and caregivers will complete a HEART visit virtually or in person. The visit includes a needs assessment that generates a tailored care plan with messages, referrals and educational materials for discussion with a nurse. Caregivers will receive brief training about the HEART App and then use the App for 4 weeks with bi-weekly real-time prompts and feedback. Heart APP: The HEART intervention includes a care planning visit for patients and caregivers and an App for caregivers focused on nutrition, self-care and support. |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | 5 individuals who enrolled did not complete the study. |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Number of Participants Meeting Patient-Caregiver Session and Care Plan Acceptability Criteria | Investigator developed questionnaire investigating acceptability of session intervention and care plan. Items were rated on a 6-point descriptive scale from strongly disagree to strongly agree. Participants that meet criteria are those that chose moderately or strongly agree. Items included: Session made me feel prepared, care plan information was helpful emotionally, care plan was helpful practically, amount of information in care plan provided was appropriate, timing of session of session was appropriate. | Posted | Number | participants | 6 week follow-up visit |
|
Baseline to 6 weeks followup
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | HEART Patients | Patients and caregivers will complete a HEART visit virtually or in person. The visit includes a needs assessment that generates a tailored care plan with messages, referrals and educational materials for discussion with a nurse. Caregivers will receive brief training about the HEART App and then use the App for 4 weeks with bi-weekly real-time prompts and feedback. Heart APP: The HEART intervention includes a care planning visit for patients and caregivers and an App for caregivers focused on nutrition, self-care and support |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Katherine R. Sterba, PhD, MPH | Medical University of South Carolina | 843- 876-2419 | sterba@musc.edu |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | Jun 17, 2021 | Nov 10, 2022 | Prot_SAP_001.pdf |
| ICF | No | No | Yes | Informed Consent Form: Patient Consent | Sep 2, 2020 | Dec 30, 2022 | ICF_002.pdf |
| ICF | No | No | Yes | Informed Consent Form: Caregiver consent | Sep 2, 2020 | Dec 30, 2022 | ICF_003.pdf |
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| ID | Term |
|---|---|
| D006258 | Head and Neck Neoplasms |
| ID | Term |
|---|---|
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
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Not provided
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| Mean Score of Unmet Needs |
30-item Cancer Survivors/Partners Unmet Needs instruments (CaSUN/ CaSPUN). Needs were endorsed on a yes/no basis, with a range of 0-30 total endorsed needs. A higher score indicates more endorsed needs. Average number of needs is reported. |
| Baseline and 6 week follow up visit |
| PROMIS Depression- Short Form (SF) v1.0 Form 8A | PROMIS Depression- SF v1.0 form 8A is an 8-item Patient-Reported Outcomes Measure Information System (PROMIS) short-form instrument. Respondents are asked how often in the past 7 days they have experienced specific depression symptoms, using a 5-point ordinal rating scale of "Never," "Rarely," "Sometimes," "Often," and "Always" whereby a higher score indicates higher depression. Raw score totals are converted to an item response theory-based T-scores. The T-score rescales the raw score into a standardized score with a mean of 50 and a standard deviation (SD) of 10 with a range of 38.2 to 81.3. Therefore, a person with a T-score of 40 is one SD below the mean. A decrease in change from baseline to 6 week followup indicates reduced depression. | Baseline and 6 week follow-up visit |
| Mean Score of Survivorship Readiness/Caregiver Preparedness | The 11-item Preparing for Life As a New Survivor (PLANS) Knowledge Subscale, developed at the University of Michigan, is utilized to evaluate survivor and caregiver (1) knowledge of diagnosis, treatment and side effects, and (2) communication with the cancer team regarding diagnosis, treatment and side effects and 3) preparedness for what to expect over the next year. Items are rated on a 6-point scale where: strongly disagree=1, moderately disagree =2, slightly disagree=3, slightly agree= 4, moderately agree=5 and strongly agree=6. Items were averaged, with a range of 1-6 with higher scores indicating higher levels of agreement. | Baseline and 6 week follow-up visit |
| Mean Score of Self-Efficacy | Based on the National Cancer Institute Follow-up Care Use Among Survivors (FOCUS) survey, two questions were asked: "How confident are you that you can get advice or information related to your/your loved one's cancer if you needed at this time?" and "How confident are you that you can (assist your loved one to) keep to the follow-up care schedule recommended by your doctors?" Participants rated items on a 5-point Likert scale where 0="Not at all confident" to 4= "Completely confident." Scores were averaged for each question, whereby higher scores indicated higher level of confidence. Change from baseline to 6 week follow up is also reported. Negative change indicates decline in self-efficacy. | Baseline and 6 week follow-up visit |
| Mean Score of Dyadic Coping/ Dyadic Efficacy | Dyadic Coping was measured using a 5-item cancer-specific subscale version of the Dyadic Coping Inventory. Items are rated on a 5-point scale from 1 ("never") to 5 ("always"). Scores were averaged with a higher score indicating a better outcome. A decrease in change between baseline and 6 week followup visit indicates worsening outcome over time. Dyadic Efficacy is an investigator developed 1-item question "How confident are you that you and your loved one can work together as a team to manage the cancer-related problems that come up?" Item was answered on a scale of 0 ("not at all confident") to 10 ("extremely confident"), with average score reported. A decrease in change between baseline and 6 week followup visit indicates worsening, where as an increase in change indicates improvement. | Baseline and 6 week follow-up visit |
| Health-Related Quality-of-Life (PROMIS Scale v1.2 - Global Health) | PROMIS Scale v1.2 - Global Health short form consists of 10 items that assess overall perceived quality of life and five general domains of health and functioning including overall physical health, mental health, social health, pain, and fatigue. Scoring uses a 5-point Likert scale with the response scores reversed (5=None to 1=Very severe) so that higher scores for responses always indicate better health. Raw scores are summed and converted to a T-score (mean score of 50, SD ± 10), Therefore a person with a T-score of 40 is one SD below the mean. A decrease in the change from baseline to 6 week follow up indicates worsening quality of life, whereas an increase indicates improvement. | Baseline and 6 week follow-up visit |
| Caregiver Burden | 4-item screening version of the Zarit Burden Interview is a self-report measure of caregiver burden. Caregivers rate each item on a 5-point Likert scale (0=never, 4= nearly always). Higher scores indicate greater caregiver distress. Total score range: 0 to 16, ≥ 8: high burden. An increase in change from baseline to 6 week follow up visit indicates increased caregiver distress. | Baseline and 6 week follow up visit |
| Ease of Mobile App Use/User Engagement | Number of weekly prompt responses missed out of 184 total expected (23 caregivers given 2 prompts per week for 4 weeks). | 4 weeks during app use |
| Number of Participants With Care Plan Use Endpoints | Number of participants of use of care plan after session, including patient and caregiver report of "Referred to Care Plan again," "Used Care Plan," "Used educational materials," and "Shared Care Plan with others." | 6 week follow up visit |
| Percentage of Participants Rating App Satisfaction/ Perceived Importance | Ratings of satisfaction with app and prompts on a 6 point descriptive rating scale ranging from strongly agree to strongly disagree. Measurements reported below are count of participants who moderately or strongly agreed with individual prompts. | 6 week follow up visit |
| Process Monitoring Data | Resources needed: Session length overall, length of nursing portion of session, length of app training- number of minutes | After session completion |
| Change From Baseline in Nutritional Status Scale | Investigator-developed 1 item: "During the past two weeks, how satisfied have you been with your nutritional status (from Extremely satisfied (1) to Not at all satisfied (5))?" | Baseline and 6 week follow up visit |
| Change From Baseline in Symptom Distress/Symptom Management | Adapted Symptom Distress Scale 1 item scaled to assess how distressing symptoms are to participant. 0= not at all distressing, 10= extremely distressing 1 item to assess patient and caregiver perceptions concerning patient ability to manage symptoms. 0= can manage extremely well, 10= cannot manage at all | Baseline and 6 week follow up visit |
| Change From Baseline in Emotional Support | PROMIS Short Form v2.0 - Emotional Support - 4a is a 4-item questionnaire. Item banks (currently adults only) assess perceived feelings of being cared for and valued as a person; having confidant relationships. PROMIS instruments are scored using item-level calibrations. Each question usually has five response options ranging in value from one to five. Raw scores are the sum of values of the response to each question then rescaled to to a standardized T-score with a mean of 50 and a standard deviation (SD) of 10. Therefore a person with a T-score of 40 is one SD below the mean. | Baseline and 6 week follow up visit |
| Change From Baseline in Symptom Severity | MD Anderson Symptom Inventory (MDASI) Head and Neck Module- Includes 13 core items and an additional 9 head and neck cancer module items which calculates a total score of symptom severity. The MDASI assesses the severity of symptoms at their worst in the last 24 hours on a 0-10 Numeric Rating Scale, with 0 being "not present" and 10 being "as bad as you can imagine." Core items and module symptom items are averaged into a mean module severity. A higher score always indicates an increase in severity. A decrease in change from baseline to 6 week follow up indicates improvement of symptoms. | Baseline and 6 week follow up visit |
| Mean |
| Full Range |
| years |
|
| Sex: Female, Male | 5 individuals who enrolled did not complete the study | Count of Participants | Participants |
|
| Ethnicity (NIH/OMB) | 5 individuals who enrolled did not complete the study | Count of Participants | Participants |
|
| Race (NIH/OMB) | 5 individuals who enrolled in the study did not complete the study. | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
|
| OG001 | HEART Caregivers | Patients and caregivers will complete a HEART visit virtually or in person. The visit includes a needs assessment that generates a tailored care plan with messages, referrals and educational materials for discussion with a nurse. Caregivers will receive brief training about the HEART App and then use the App for 4 weeks with bi-weekly real-time prompts and feedback. Heart APP: The HEART intervention includes a care planning visit for patients and caregivers and an App for caregivers focused on nutrition, self-care and support |
|
|
| Primary | Intervention Delivery/ Fidelity | Number of caregivers receiving all session content and delivery of the intervention as planned (intro to session, nurse care plan discussion, viewed nutritional support video, app training). | Posted | Count of Participants | Participants | 6 week follow up visit |
|
|
|
| Primary | Intervention Reach | Percentage of those recruited who completed baseline and 6 week follow up surveys and the intervention session. | 50 enrolled, 4 lost to follow up | Posted | Count of Participants | Participants | Baseline and 6 week follow up visit |
|
|
|
| Secondary | Ease of Use/System Usability | System Usability Scale (SUS) - The SUS consists of a 10 item questionnaire with five response options for respondents; from Strongly agree to Strongly disagree. Scores range from 0-100, with higher scores indicating better usability. | System Usability Scale only measured in Caregivers. | Posted | Mean | Full Range | score on a scale | 6 week follow up visit only (no baseline comparison) |
|
|
|
| Secondary | Mean Score of Unmet Needs | 30-item Cancer Survivors/Partners Unmet Needs instruments (CaSUN/ CaSPUN). Needs were endorsed on a yes/no basis, with a range of 0-30 total endorsed needs. A higher score indicates more endorsed needs. Average number of needs is reported. | Posted | Mean | Full Range | score on a scale | Baseline and 6 week follow up visit |
|
|
|
| Secondary | PROMIS Depression- Short Form (SF) v1.0 Form 8A | PROMIS Depression- SF v1.0 form 8A is an 8-item Patient-Reported Outcomes Measure Information System (PROMIS) short-form instrument. Respondents are asked how often in the past 7 days they have experienced specific depression symptoms, using a 5-point ordinal rating scale of "Never," "Rarely," "Sometimes," "Often," and "Always" whereby a higher score indicates higher depression. Raw score totals are converted to an item response theory-based T-scores. The T-score rescales the raw score into a standardized score with a mean of 50 and a standard deviation (SD) of 10 with a range of 38.2 to 81.3. Therefore, a person with a T-score of 40 is one SD below the mean. A decrease in change from baseline to 6 week followup indicates reduced depression. | Posted | Mean | Full Range | T-Score | Baseline and 6 week follow-up visit |
|
|
|
| Secondary | Mean Score of Survivorship Readiness/Caregiver Preparedness | The 11-item Preparing for Life As a New Survivor (PLANS) Knowledge Subscale, developed at the University of Michigan, is utilized to evaluate survivor and caregiver (1) knowledge of diagnosis, treatment and side effects, and (2) communication with the cancer team regarding diagnosis, treatment and side effects and 3) preparedness for what to expect over the next year. Items are rated on a 6-point scale where: strongly disagree=1, moderately disagree =2, slightly disagree=3, slightly agree= 4, moderately agree=5 and strongly agree=6. Items were averaged, with a range of 1-6 with higher scores indicating higher levels of agreement. | Posted | Mean | Full Range | score on a scale | Baseline and 6 week follow-up visit |
|
|
|
| Secondary | Mean Score of Self-Efficacy | Based on the National Cancer Institute Follow-up Care Use Among Survivors (FOCUS) survey, two questions were asked: "How confident are you that you can get advice or information related to your/your loved one's cancer if you needed at this time?" and "How confident are you that you can (assist your loved one to) keep to the follow-up care schedule recommended by your doctors?" Participants rated items on a 5-point Likert scale where 0="Not at all confident" to 4= "Completely confident." Scores were averaged for each question, whereby higher scores indicated higher level of confidence. Change from baseline to 6 week follow up is also reported. Negative change indicates decline in self-efficacy. | Posted | Mean | Full Range | score on a scale | Baseline and 6 week follow-up visit |
|
|
|
| Secondary | Mean Score of Dyadic Coping/ Dyadic Efficacy | Dyadic Coping was measured using a 5-item cancer-specific subscale version of the Dyadic Coping Inventory. Items are rated on a 5-point scale from 1 ("never") to 5 ("always"). Scores were averaged with a higher score indicating a better outcome. A decrease in change between baseline and 6 week followup visit indicates worsening outcome over time. Dyadic Efficacy is an investigator developed 1-item question "How confident are you that you and your loved one can work together as a team to manage the cancer-related problems that come up?" Item was answered on a scale of 0 ("not at all confident") to 10 ("extremely confident"), with average score reported. A decrease in change between baseline and 6 week followup visit indicates worsening, where as an increase in change indicates improvement. | Posted | Mean | Full Range | score on a scale | Baseline and 6 week follow-up visit |
|
|
|
| Secondary | Health-Related Quality-of-Life (PROMIS Scale v1.2 - Global Health) | PROMIS Scale v1.2 - Global Health short form consists of 10 items that assess overall perceived quality of life and five general domains of health and functioning including overall physical health, mental health, social health, pain, and fatigue. Scoring uses a 5-point Likert scale with the response scores reversed (5=None to 1=Very severe) so that higher scores for responses always indicate better health. Raw scores are summed and converted to a T-score (mean score of 50, SD ± 10), Therefore a person with a T-score of 40 is one SD below the mean. A decrease in the change from baseline to 6 week follow up indicates worsening quality of life, whereas an increase indicates improvement. | Posted | Mean | Full Range | T-Score | Baseline and 6 week follow-up visit |
|
|
|
| Secondary | Caregiver Burden | 4-item screening version of the Zarit Burden Interview is a self-report measure of caregiver burden. Caregivers rate each item on a 5-point Likert scale (0=never, 4= nearly always). Higher scores indicate greater caregiver distress. Total score range: 0 to 16, ≥ 8: high burden. An increase in change from baseline to 6 week follow up visit indicates increased caregiver distress. | Change in mean score from baseline to six weeks measured in caregivers only | Posted | Mean | Full Range | units on a scale | Baseline and 6 week follow up visit |
|
|
|
|
| Secondary | Ease of Mobile App Use/User Engagement | Number of weekly prompt responses missed out of 184 total expected (23 caregivers given 2 prompts per week for 4 weeks). | Measured in Caregivers only. (23 caregivers given 2 prompts per week for 4 weeks= 184 prompts). | Posted | Number | number of missed prompts | 4 weeks during app use | prompts | prompts |
|
|
|
| Secondary | Number of Participants With Care Plan Use Endpoints | Number of participants of use of care plan after session, including patient and caregiver report of "Referred to Care Plan again," "Used Care Plan," "Used educational materials," and "Shared Care Plan with others." | Posted | Count of Participants | Participants | 6 week follow up visit |
|
|
|
| Secondary | Percentage of Participants Rating App Satisfaction/ Perceived Importance | Ratings of satisfaction with app and prompts on a 6 point descriptive rating scale ranging from strongly agree to strongly disagree. Measurements reported below are count of participants who moderately or strongly agreed with individual prompts. | Posted | Count of Participants | Participants | 6 week follow up visit |
|
|
|
| Secondary | Process Monitoring Data | Resources needed: Session length overall, length of nursing portion of session, length of app training- number of minutes | Posted | Mean | Full Range | minutes | After session completion |
|
|
|
| Secondary | Change From Baseline in Nutritional Status Scale | Investigator-developed 1 item: "During the past two weeks, how satisfied have you been with your nutritional status (from Extremely satisfied (1) to Not at all satisfied (5))?" | Posted | Mean | Full Range | score on a scale | Baseline and 6 week follow up visit |
|
|
|
| Secondary | Change From Baseline in Symptom Distress/Symptom Management | Adapted Symptom Distress Scale 1 item scaled to assess how distressing symptoms are to participant. 0= not at all distressing, 10= extremely distressing 1 item to assess patient and caregiver perceptions concerning patient ability to manage symptoms. 0= can manage extremely well, 10= cannot manage at all | Posted | Mean | Full Range | score on a scale | Baseline and 6 week follow up visit |
|
|
|
| Secondary | Change From Baseline in Emotional Support | PROMIS Short Form v2.0 - Emotional Support - 4a is a 4-item questionnaire. Item banks (currently adults only) assess perceived feelings of being cared for and valued as a person; having confidant relationships. PROMIS instruments are scored using item-level calibrations. Each question usually has five response options ranging in value from one to five. Raw scores are the sum of values of the response to each question then rescaled to to a standardized T-score with a mean of 50 and a standard deviation (SD) of 10. Therefore a person with a T-score of 40 is one SD below the mean. | Posted | Mean | Full Range | T-Score | Baseline and 6 week follow up visit |
|
|
|
| Secondary | Change From Baseline in Symptom Severity | MD Anderson Symptom Inventory (MDASI) Head and Neck Module- Includes 13 core items and an additional 9 head and neck cancer module items which calculates a total score of symptom severity. The MDASI assesses the severity of symptoms at their worst in the last 24 hours on a 0-10 Numeric Rating Scale, with 0 being "not present" and 10 being "as bad as you can imagine." Core items and module symptom items are averaged into a mean module severity. A higher score always indicates an increase in severity. A decrease in change from baseline to 6 week follow up indicates improvement of symptoms. | Posted | Mean | Full Range | score on a scale | Baseline and 6 week follow up visit |
|
|
|
| 0 |
| 23 |
| 0 |
| 23 |
| 0 |
| 23 |
| EG001 | HEART Caregivers | Patients and caregivers will complete a HEART visit virtually or in person. The visit includes a needs assessment that generates a tailored care plan with messages, referrals and educational materials for discussion with a nurse. Caregivers will receive brief training about the HEART App and then use the App for 4 weeks with bi-weekly real-time prompts and feedback. Heart APP: The HEART intervention includes a care planning visit for patients and caregivers and an App for caregivers focused on nutrition, self-care and support | 0 | 23 | 0 | 23 | 0 | 23 |
Not provided
Not provided
|
| Black or African American |
|
| White |
|
| More than one race |
|
| Unknown or Not Reported |
|
| Change from baseline to 6 week follow up visit |
|
| Change from baseline to 6 week follow up visit |
|
| Change from baseline to 6 weeks follow up |
|
| Change- Self Efficacy: confidence in obtaining cancer related advice/adhering to follow up care |
|
| Baseline- Self Efficacy: adhering to recommended follow up care |
|
| 6 week f/u visit- Self Efficacy: adhering to recommended follow up care |
|
| Change - Self Efficacy: adhering to recommended follow up care |
|
| Dyadic Coping: Change from baseline to 6 week follow up |
|
| Dyadic Efficacy: Baseline |
|
| Dyadic Efficacy: 6 week follow up visit |
|
| Dyadic Efficacy: Change from baseline to 6 week follow up |
|
| 6 week follow up visit |
|
| Change from baseline to 6 week follow up visit |
|
|
| Used educational materials |
|
| Shared Care Plan with others |
|
| App provided practical tips |
|
| Amount of app information was appropriate |
|
|
| Change from baseline to 6 week follow up visit |
|
| Symptom Distress: Baseline to 6 week follow up visit |
|
| Symptom Management: Baseline |
|
| Symptom Management: 6 week follow up |
|
| Symptom Management: Baseline to 6 week follow up visit |
|
| Change from baseline to 6 week follow up visit |
|
|