Implementation of PrEP Care Among Women in Family Planning Clinics

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-45
SponsorRush University Medical Center

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Eligible participants include ciswomen presenting at a PPIL health center with a positive STI test (syphilis, gonorrhea, or chlamydia) and identified in the EHR using STI testing records and new fields for optimizing support of provider PrEP counseling.

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • POWER Up strategies -

    Behavioral

    Clinics will implement adapted POWER Up intervention strategies when a patient is flagged as PrEP eligible.

Treatment groups

250 Participants
are divided into 2 treatment groups
Group A: Intervention - Aim 2Experimental treatment 1 intervention
Group B: Control - Aim 2No intervention 0 interventions

Trial outcomes

Primary outcomes

1

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.

Time frame
1 month

Secondary outcomes

1

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.

Time frame
6 months

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Rush University Medical Center

Lead sponsor

National Institute of Mental Health (NIMH)

Collaborator

University of Illinois at Chicago

Collaborator

Planned Parenthood of Illinois

Collaborator

This trial is not recruiting at the moment. You can still explore other options: