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N/A N=19 Prevention

Developing an Online Mindfulness-based Intervention to Reduce Minority Stress and HIV Risk Among Young Adult MSM

HIV · Minority Stress · Mental Health Wellness 1

Enrolled (actual)
19
Serious AEs
0.0%
Results posted
Nov 2025
Primary outcome: Primary: Feasibility of Online Mindfulness-Based Queer Resilience as Measured by Recruitment Rates — 19 Participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Mindfulness-Based Queer Resilience (MBQR) (Behavioral)
Age
Adult · 18+ yrs
Sex
Male
Sponsor
Brown University
Primary completion
Dec 2022

Outcome Measures

OutcomeResultp-value
PRIMARY
Feasibility of Online Mindfulness-Based Queer Resilience as Measured by Recruitment Rates
19
PRIMARY
Feasibility of Online Mindfulness-Based Queer Resilience as Measured by Retention Rates
18; 15
PRIMARY
Feasibility of Online Mindfulness-Based Queer Resilience as Measured by Session Attendance and Home Practice Completion
5.84; 5.32
PRIMARY
Acceptability of Online Mindfulness-Based Queer Resilience as Measured by the Client Satisfaction Questionnaire
26.17
PRIMARY
Acceptability of Online Mindfulness-Based Queer Resilience as Measured by a Session Evaluation Form
16.17

Summary

The overall aim of the research study is to develop and test a mindfulness-based program for young adult gay, bisexual, and queer men at risk for HIV (Brown University IRB approved protocol #2004002698). Researchers have completed Aim 1 of the broader study, which was to use qualitative, community engaged methods, along with a quantitative online survey, to inform intervention development with the study population. The next phase of the intervention development (Aim 2 - registered here), involves seeking feedback on the developed mindfulness program through an open-pilot with 18 participants from the same study population (young adult gay, bisexual, and queer men at risk for HIV).

Eligibility Criteria

Inclusion Criteria

  • Assigned male at birth
  • Being 18 to 34 years of age
  • Identify as a cisgender man
  • Reside in the United States
  • Can read and speak in English
  • Engaged in condomless anal sex with another man in the past 6-months
  • Endorse distress, measured by the PHQ-9 and GAD-7
  • Possess a device (phone, tablet, computer) that allows for online conferencing
  • HIV-negative or status unknown (self-report)

Exclusion Criteria: Participants will be excluded from the study if they are determined to have symptoms preventing them from giving meaningful consent or study activities such as:

  • Significant cognitive impairment
  • Psychosis
  • Imminent suicidal risk
  • Substance abuse
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05540652). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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