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| ID | Type | Description | Link |
|---|---|---|---|
| 1R01MH134264 | U.S. NIH Grant/Contract | View source |
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| Name | Class |
|---|---|
| National Institute of Mental Health (NIMH) | NIH |
| University of Illinois at Chicago | OTHER |
| Planned Parenthood of Illinois | UNKNOWN |
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This study will evaluate implementation strategies to address barriers and increase uptake of PrEP among Black cisgender women in Planned Parenthood of Illinois (PPIL) health centers.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Intervention - Aim 2 | Experimental | During the intervention period, PPIL staff will capture PrEP eligible women through an updated electronic flag alert in the patient's electronic medical record. The flag will alert to offer the patient PrEP navigation services and implement adapted POWER Up intervention strategies according to training. |
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| Control - Aim 2 | No Intervention | PPIL health centers will follow current PrEP navigation procedures using current monitoring system. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| POWER Up strategies - | Behavioral | Clinics will implement adapted POWER Up intervention strategies when a patient is flagged as PrEP eligible. |
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| Measure | Description | Time Frame |
|---|---|---|
| PrEP prescriptions among Black women accessing PPIL services and eligible for PrEP. | PrEP eligibility among Black women will be defined based on positive STI test and identified in the EHR using STI testing records and new fields for optimizing support of provider PrEP counseling. Using de-identified patient-level EHR data for eligible women at each clinic within each time point, we will create a dichotomous variable for having received a prescription for PrEP during a given time period. | 1 month |
| Measure | Description | Time Frame |
|---|---|---|
| Receipt of PrEP refills among Black women accessing FP services at 6 months. | Using de-identified patient-level EHR data for eligible patients at each clinic within each time point, we will create a dichotomous variable for receiving refills of prescriptions for PrEP of those with an initial PrEP prescription. | 6 months |
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Inclusion Criteria:
Exclusion Criteria:
- Participants will be excluded if they are not PrEP eligible, have a negative STI test, or are not identified in the EHR.
Ciswomen will be eligible for participation in this study.
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Cristina MA Barkowski, MSW | Contact | 312-942-6382 | cristina_m_barkowski@rush.edu | |
| Kate P Palmer, MPH | Contact | 312-563-9389 | kate_p_palmer@rush.edu |
| Name | Affiliation | Role |
|---|---|---|
| Sadia Haider, MD, MPH | Rush University Medical Center | Principal Investigator |
| Amy Johnson, PhD, MSW | Ann and Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine | Principal Investigator |
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