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NCT05262426Completed

Developing mHealth to Promote PrEP Use Among Thai Young Vulnerable Adolescents and Emerging Adults

Optimizing an mHealth Intervention to Improve Uptake and Adherence of the HIV Pre-exposure Prophylaxis (PrEP) in Vulnerable Adolescents and Emerging Adults

Source: ClinicalTrials.gov · Last updated 8 Sept 2026

Brief summary (registry, in English)

The main aim of this study is to develop technology-based interventions to improve HIV pre-exposure prophylaxis (PrEP) uptake and adherence among Thai young transgender women.

Status (registry)
Completed
Study type
Interventional
Enrollment
145 (actual)
First submitted
7 Feb 2022
Start date
27 Dec 2021
Primary completion date
31 Jan 2026
Lead sponsor
University of Massachusetts, Worcester
Diseases
HIV
NCT number
NCT05262426

What you commit to

  • Study type: Interventional
  • Participants enrolled: 145
  • From 27 Dec 2021 to the primary completion date, 31 Jan 2026
  • 3 sites 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 illness

  • Have a serious cognitive or psychiatric problem that would compromise ability to provide informed consent
  • Have active suicidal ideation or major mental illness (e.g., untreated psychosis or mania) at the time of interview (patients will be referred for treatment)
  • Have a serious cognitive or psychiatric problem that would compromise ability to provide informed consent
  • Have active suicidal ideation or major mental illness (e.g., untreated psychosis or mania) at the time of interview (patients will be referred for treatment)
  • Currently enrolled in another HIV intervention study

Lab values

  • Laboratory or clinical findings that would preclude PrEP initiation (e.g., decreased creatinine clearance)
    • Healthcare providers
  • Laboratory or clinical findings that would preclude PrEP initiation (e.g., decreased creatinine clearance)

Other

  • None
    • Aim 2:

Who the study is looking for

  • Age 16-29 years old
  • Male sex at birth
  • Self-identifies as woman or transgender women or culturally identifies with the female spectrum
  • Confirmed HIV-negative status
  • Self-reported recent history of condomless sex in the past 6 months
  • Able to understand, read and speak Thai
  • Either having not started PrEP (Group 1: PrEP naive), currently on PrEP but not adherent to PrEP (taking ≤3 pills/week) in the past month (Group 2: PrEP users) or currently on PrEP with good adherence (Group 3: PrEP users with good adherence).
  • Have at least 1-year experience working with HIV-negative transgender women, including providing PrEP prescription and counseling
  • Age 16-29 years old
  • Male sex at birth
  • Self-identifies as woman or transgender women or culturally identifies with the female spectrum
  • Confirmed HIV-negative status
  • Self-reported recent history of condomless sex in the past 6 months
  • Able to understand, read and speak Thai
  • Either having not started PrEP (Group 1: PrEP naive), currently on PrEP but not adherent to PrEP (taking ≤3 pills/week) in the past month (Group 2: PrEP users).

Criteria the registry did not label

  • Aim 1:
  • Transgender women participants

Age in the registry: 16 years to 29 years · Sex: Male · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Institute of HIV Research and Innovation
Coordinator of this site? Confirm its status
BangkokThailandUnknown status
SWING Foundation
Coordinator of this site? Confirm its status
BangkokThailandUnknown status
Rainbow Sky Association of Thailand
Coordinator of this site? Confirm its status
BangkokThailandUnknown status

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