Improving Health Outcomes for Women Living With HIV

Not Applicable

Completed

• Conditions: HIV/AIDS
• Interventions: Behavioral: Peer Navigation

• Registration Number: NCT03525340
• Lead Sponsor: University of California, San Francisco

Brief Summary

This study will develop and conduct a trans-specific peer navigation intervention in Brazil, which integrates the I-Care approach developed in South Africa with the Model of Gender Affirmation (GA), developed by the investigators to specifically address HIV prevention and care among trans women.

Detailed Description

Globally, transgender ('trans') women have 49 times higher odds of HIV infection compared to other groups and trans women living with HIV (TWH) access HIV care and adhere to medication at significantly lower rates than other at-risk groups. Poor engagement in HIV care for TWH is a result of reduced access to and avoidance of healthcare due to stigma and negative experiences with providers, and occurs in the context of social and economic marginalization that foments unstable employment and housing, familial alienation, limited social support, and substance abuse. Interventions to mitigate these barriers to care are critical to reducing HIV-related disparities and poor health outcomes for this highly vulnerable population, particularly where disparities are most apparent, including Brazil. Peer-based navigation (PN) interventions have demonstrated success in improving engagement in HIV care in low-resource settings. The investigators recently conducted a PN intervention ('I-Care') in rural South Africa that significantly improved both linkage to care and retention for men and women. While the PN intervention addresses HIV care engagement by providing social support and skills to work with health providers and family, it requires specific adaptation and a conceptual model that addresses the unique needs of TWH identified during formative research and in consultations with Brazilian stakeholders in 2015. The investigators propose to develop and conduct a trans-specific PN intervention in Brazil, tentatively named 'TransAmigas', which integrates the I-Care approach with the Model of Gender Affirmation (GA), developed by the research team to specifically address HIV prevention and care among trans women. The investigators will use the ADAPT-ITT methodology to develop TransAmigas, incorporating the GA model in the Brazilian context (Aim 1). The investigators will then conduct a pilot study to test the feasibility and acceptability of TransAmigas in São Paulo, Brazil (Aim 2) by randomizing TWH to the intervention (n=100) or to clinical referral (n=50). During the nine month pilot, the investigators will track both navigator and patient adherence to the program, recruitment needs, cohort retention, and reported satisfaction and preferences for program content through surveys at baseline and nine months. Finally, the investigators will prepare for a multi-site efficacy trial (Aim 3) by extracting clinical data from participants' records at the referral clinic, generating preliminary efficacy data by comparing retention in HIV care and viral load by intervention arm. Clinical data will inform future trial sample size. The study will be implemented in Sao Paulo, Brazil, where universal access to care and public support for gender transition care provide an enabling environment for this work to be most effective and where the team has established academic partnerships and a collaboration with the State-run reference and training clinical site (CRT), which includes trans-specific clinical services. If feasible, acceptable, and ultimately proven efficacious, TransAmigas will be the first evidence-based HIV care intervention for TWH globally - filling a crucial gap in programming.

Study Timeline

• Study First Submitted: 2018-02-28
• Study First Submitted QC: 2018-05-02
• Study Start: 2018-05-07
• Study First Posted: 2018-05-15
• Primary Completion: 2019-10-15
• Study Completion: 2019-10-15
• Status Verified: 2019-11
• Last Update Submitted: 2019-11-20
• Last Update Posted: 2019-11-22

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Male
• Target Recruitment: 113

Inclusion Criteria

• have either a recent HIV diagnosis (within the prior 12 months) or be out of care for previously diagnosed HIV
• be a resident of the São Paulo area
• consent for study staff to review their clinical records

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Exclusion Criteria

• female sex at birth
• less than 18 years of age
• not HIV-positive
• currently engaged in care
• unable to provide informed consent
• reside outside of the São Paulo area

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Peer Navigation	Peer Navigation	Participants in the peer navigation arm will meet with a peer navigator at least once per month for nine months in-person, and have at least one other navigator contact per month. Like the standard of care arm, they will provide informed consent, respond to baseline and endline surveys, and have clinic record data extracted for the 9 months of their study participation.

Primary Outcome Measures

Name	Time	Method
Acceptability of Peer Navigation Intervention	Baseline	Proportion of transgender women offered navigation services who accept invitation

Secondary Outcome Measures

Name	Time	Method
Feasibility of Peer Navigation Intervention: Enrollment rate	At 9 months	Proportion of transgender women living with HIV who are screened, eligible, enrolled, and successfully complete navigation.
Trial Planning - Linkage to confirmatory testing	At 9 months	Time from diagnosis to CD4+ T-cell count results
Trial Planning - Adherence	At 9 months	Proportion of days covered (# of dispensed days of medication / # of days between refills)
Trial Planning - Retention	At 9 months	Proportion of patients who remain on treatment following 9 months of enrollment in pilot
Trial Planning - Viral Suppression	At 9 months	Proportion of participants with viral load 1) undetectable and 2) below 1000 copies/mL
Feasibility of Peer Navigation Intervention: Patient Satisfaction	At 9 months	Proportion in TransAmigas who report satisfaction with navigation quality, duration, contact schedule, thematic content, support.
Trial Planning - Defaulting	At 9 months	Proportion of participants not in care 90 days after prescribed medication estimated to last 90
Feasibility of Peer Navigation Intervention: Navigator Retention	At 9 months	Proportion of navigators who remain in program.
Trial Planning - Linkage to ART	At 9 months	Time from diagnosis to antiretroviral therapy initiation

Trial Locations

Locations (1)

Santa Casa Medical School; 🇧🇷 São Paulo, Brazil