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Completed

NCT Number: NCT03525340

Improving Health Outcomes for Women Living With HIV

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.

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Key information

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

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

Treatment and study plan

Peer navigation

Behavioral

Peer navigators help participants identify barriers that pose challenges to the participant's engagement in care and adherence and help develop an overall action plan for addressing these barriers by identifying specific changes that can be made/attempted to overcome an identified barrier. This may involve accompanying a participant to their social services/health appointments, or assisting a participant with disclosure of her HIV status to a family member or friend. The overall goal is to develop knowledge of social/HIV-related health services and good problem-solving skills in order to tackle multiple, potentially overlapping barriers. Over time, participants are encouraged to take increasing degrees of responsibility for identifying and implementing their own problem-solving strategies.

Primary outcomes

  1. Acceptability of Peer Navigation Intervention

    Time frame: Baseline

    Proportion of transgender women offered navigation services who accept invitation

Secondary outcomes

  1. Feasibility of Peer Navigation Intervention: Patient Satisfaction

    Time frame: At 9 months

    Proportion in TransAmigas who report satisfaction with navigation quality, duration, contact schedule, thematic content, support.

  2. Feasibility of Peer Navigation Intervention: Enrollment rate

    Time frame: At 9 months

    Proportion of transgender women living with HIV who are screened, eligible, enrolled, and successfully complete navigation.

  3. Feasibility of Peer Navigation Intervention: Navigator Retention

    Time frame: At 9 months

    Proportion of navigators who remain in program.

  4. Trial Planning - Linkage to ART

    Time frame: At 9 months

    Time from diagnosis to antiretroviral therapy initiation

  5. Trial Planning - Linkage to confirmatory testing

    Time frame: At 9 months

    Time from diagnosis to CD4+ T-cell count results

  6. Trial Planning - Retention

    Time frame: At 9 months

    Proportion of patients who remain on treatment following 9 months of enrollment in pilot

  7. Trial Planning - Defaulting

    Time frame: At 9 months

    Proportion of participants not in care 90 days after prescribed medication estimated to last 90

  8. Trial Planning - Adherence

    Time frame: At 9 months

    Proportion of days covered (# of dispensed days of medication / # of days between refills)

  9. Trial Planning - Viral Suppression

    Time frame: At 9 months

    Proportion of participants with viral load 1) undetectable and 2) below 1000 copies/mL

Sponsors and collaborators

Lead sponsor

University of California, San Francisco

Other

Collaborators

  • National Institute of Mental Health (NIMH)

Registry information

Official study title

Improving Health Outcomes for HIV-Positive Women in Brazil

Important dates

Study start
2018
Primary completion
2019
Study completion
2019
First posted
May 15, 2018
Registry last updated
Nov 22, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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