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Not yet recruiting NCT06335121

Implementation of PrEP Care Among Women in Family Planning Clinics

No phase Interventional PrEP Uptake HIV Prevention

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: POWER Up strategies -.
Who it may be relevant to
Registry conditions: PrEP Uptake, HIV, Prevention. Basic parameters: 18 years — 45 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

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.

Interventions

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

Primary outcome measures

  • PrEP prescriptions among Black women accessing PPIL services and eligible for PrEP. [Time frame: 1 month]
Secondary outcome measures (1)
  • Receipt of PrEP refills among Black women accessing FP services at 6 months. [Time frame: 6 months]

Eligibility criteria

Inclusion criteria

  • 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.

Exclusion criteria

\- Participants will be excluded if they are not PrEP eligible, have a negative STI test, or are not identified in the EHR.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Health services research

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06335121 · 21120602 · 1R01MH134264

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗