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NCT05799339Completed

Optimizing CAB-LA as PrEP for Women Who Inject Drugs

Exploring Engagement and Opportunities to Optimize CAB-LA as Pre-exposure Prophylaxis (PrEP) for Women Who Inject Drugs

Source: ClinicalTrials.gov · Last updated 29 Dec 2025

Brief summary (registry, in English)

The goal of this study is to elicit information crucial for designing strategies to support engagement in cabotegravir, a long-acting injectable form of pre-exposure prophylaxis (PrEP) to reduce HIV risk among women who inject drugs (WWID), a population with high unmet need that has been understudied in all phases of PrEP research. The main questions this study aims to answer are: 1. How do WWID perceive long-acting injectable cabotegravir (CAB-LA) as a HIV prevention tool? 2. If and how their decisions to initiate CAB-LA as PrEP are informed by their experiences with other long-acting medications, experience with daily oral medications, and their personal circumstance (e.g., like housing or addition severity)? 3. Do PrEP outcomes (e.g., adherence) and engagement in care over time differ between WWID prescribed CAB-LA versus daily oral PrEP? The sample for this study will be derived from and ongoing prospective trial of "TIARAS," a multi-component behavioral intervention designed to reduce HIV acquisition risk among women who inject drugs (see NCT05192434).

Status (registry)
Completed
Study type
Observational
Enrollment
144 (actual)
First submitted
23 Mar 2023
Start date
Jan 2022
Primary completion date
Jul 2025
Lead sponsor
Alexis Roth
Diseases
HIV
NCT number
NCT05799339

What you commit to

  • Study type: Observational
  • Participants enrolled: 144
  • From Jan 2022 to the primary completion date, Jul 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Unable to provide informed consent

Who the study is looking for

  • HIV-negative cisgender female
  • age ≥ 18 years
  • speaks/reads English
  • reporting past 6 months day non-prescription injection drug use
  • enrolled in the TIARAS trial (NCT05192434)

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Prevention Point Philadelphia
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.