PLUS PINK: HHRP+ Adaptation for Women With HIV Under Community Supervision
Completed · Not applicable
Conditions studied: HIV
In brief
After enrollment, participants will be randomized to either receive the intervention (treatment) from trained health educators or undergo observation as usual (control group). Randomization will be stratified by HIV serostatus. A control group is appropriate because participants will still receive services offered through probation and will be offered the intervention after completion of the trial. Subjects will be paid, not for participating in the intervention, but for providing research assessments. The newly adapted intervention will be delivered over no more than a 3-month period (it will be shorter if the adaptation process is supportive). Baseline assessments will assess the pre-intervention period. The 3-month assessment will be the end-of-intervention effects and the post-intervention assessments will be at 6, 9 and 12 months. HIV prevention knowledge will be assessed based on quizzes used previously for HHRP+; though final quiz content will depend on final selected materials for the intervention. Subjects will be followed for 12 months with assessments by trained research assistants.
Key facts
- Study ID
- NCT03175094
- Run by
- Yale University
- People needed
- 90
- Starts
- 2015-03-03
- Expected to finish
- 2017-11-10
- Last updated by the study team
- 2021-08-04
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- age ≥18 years old
- female
- have laboratory confirmed HIV OR are at-risk for HIV (ever injected drugs, ever engaged in commercial sex work, were incarcerated in prison or jail within the past 2 years, had condomless sex with an HIV+ partner or partner whose HIV status is unknown in the past 90 days, or had a diagnosed sexually transmitted infection in the past 90 days),
- and are under or anticipating transfer to probation.are either a) sentenced to probation or on intensive pretrial supervision by a probation officer; b) sentenced to parole; or c) incarcerated in jail or prison in the prior 60 days.
- Potential participants will be excluded
You may not qualify if…
- unable or unwilling to provide informed consent,
- have <3 months of remaining scheduled supervision term,
- or are threatening to staff
Where it is running
- Yale AIDS Program — New Haven, Connecticut, United States
Full record on ClinicalTrials.gov
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