CClinicalTrials.gg
CompletedNCT05855655MBQRUpdated Nov 24, 2025Results posted

Developing an Online Mindfulness-based Intervention to Reduce Minority Stress and HIV Risk Among Young Adult MSM - Aim 3

An interventional study of Mindfulness-Based Queer Resilience (MBQR) in Hiv, Minority Stress and Mental Health Wellness 1, sponsored by Brown University. Completed at 1 site in United States. Open to male participants aged 18 Years to 34 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-11-24.

Sponsored by Brown University · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
68
Allocation
Randomized
Ages
18 Years to 34 Years
Sex
Male
01

Study 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 Aims 1 and 2 of the broader study. Aim 1 used qualitative, community engaged methods, along with a quantitative online survey, to inform intervention development with the study population. Aim 2 involved 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). The next phase of the intervention development (Aim 3 - registered here) will enroll and randomize a sample of 60 distressed, high-risk YMSM into one of two groups: MBQR intervention (n=30) or active control condition (n=30). Researchers aim to over-enroll YMSM of color (e.g., Black/Latinx YMSM) and anticipate the group to include approximately 50-60% Black/Latinx YMSM (or YMSM of color). Outcomes of feasibility and acceptability include rates of recruitment and retention, number of sessions attended, self-reported at-home practice of mindfulness, completion of assessment, and exit interviews.

Read the detailed description

In 2017, gay, bisexual, and other men who have sex with men (MSM) made up 70% of new HIV infections in the U.S., and young adult MSM (age 18-34; YMSM) account for the majority of HIV cases. YMSM also experience prevalent, often co-occurring mental health issues, including depression, anxiety, and substance use, creating a "syndemic" condition surrounding HIV risk and suboptimal HIV testing.

A key driver of such disparities experienced by YMSM is minority stress. Experiences of identity-based discrimination lead to internalized stigma and maladaptive coping (e.g., emotion dysregulation, avoidant coping, impulsivity) The "downstream" effects of minority stress are poor mental health (depression and anxiety), increased sexual risk, and lack of engagement in key health services such as HIV testing due to anxiety related to identity disclosure to providers and anticipation of stigmatizing encounters. Recent evidence also suggests discrimination exposure is linked to heightened physiological stress response (cortisol level) that represents depletion of coping resources and increased risk for development of stress-linked psychological disorders (depression, anxiety). Therefore, reducing minority stress represents a promising transdiagnostic approach to reduce the burden of HIV and mental health issues experienced by YMSM.

Research suggests that Mindfulness-Based Interventions (MBIs) target mechanisms relevant to minority stress, including self-acceptance, emotional dysregulation, and avoidant coping. Therefore, as an individual-level intervention, MBIs may serve as an innovative HIV prevention intervention by lowering the syndemic risk among YMSM through reducing psychological symptoms, improving coping, and enhancing HIV-related behavioral health. However, no evidence-based MBIs have been tested for HIV prevention, and clinical and research evidence suggests further adaptation is warranted to improve its relevance and optimize engagement for YMSM.

This study aims to develop an internet-delivered MBI to address minority stress and its negative HIV-related health consequences experienced by YMSM. Specifically, the researchers propose to adapt, refine, and pilot-test an evidence-based MBI, Mindfulness-based Stress Reduction (MBSR), to promote mental and sexual health and HIV testing engagement among distressed, high-risk YMSM. Aims 1-3 will support the subsequent production and evaluation of the adapted intervention. To maximize reach, scalability, and availability to a population that experience challenges seeking in-person counseling and health services, the intervention will also be adapted for internet-based delivery.

Aim 1. (Previously Completed) Adapt MBSR for distressed, high-risk YMSM using internet delivery, guided by the ADAPT-ITT model. Researchers conducted iterative phases of formative research including online-based focus groups with YMSM, solicitation of feedback from stakeholders, and revision of intervention protocols. This process resulted in the first-draft of an internet-delivered, mindfulness-based intervention protocol for use with YMSM, known as "Mindfulness-Based Queer Resilience (MBQR)".

Aim 2. (Previously Completed - see ClinicalTrials.gov ID: NCT05540652) Refine intervention protocol by administering adapted materials to distressed, high-risk YMSM (n=18) through internet-based open pilot and gather feedback. Following integration of feedback, this process will result in a finalized protocol of an internet-delivered, mindfulness-based intervention protocol for YMSM.

Aim 3. (This is the focus of this Clinical Trial Registration) Examine the feasibility and acceptability of the internet-delivered mindfulness-based intervention (iMBI), called "Mindfulness-based Queer Resilience (MBQR)", for HIV prevention. Researchers will enroll and randomize a sample of 60 distressed, high-risk YMSM into one of two groups: MBQR intervention (n=30) or active control condition (n=30). They will aim to over-enroll YMSM of color (e.g., Black/Latinx YMSM) and anticipate the group to include approximately 50-60% Black/Latinx YMSM (or YMSM of color). The study will examine outcomes of feasibility and acceptability, such as rates of recruitment and retention, number of sessions attended, self-reported at-home practice of mindfulness, completion of assessment, and exit interviews.

02

Conditions studied

  • Hiv
  • Minority Stress
  • Mental Health Wellness 1

Keywords

  • Mindfulness-based intervention
  • Sexual minority
  • LGBTQ
  • HIV prevention
03

In context

Acquired Immunodeficiency Syndrome

2,040 studies on the registry are indexed under Acquired Immunodeficiency Syndrome; 272 are open to participants now.

This study's enrollment of 68 is below the median of 105 across 1,543 interventional studies indexed under Acquired Immunodeficiency Syndrome.

Browse Acquired Immunodeficiency Syndrome studies →

Lead sponsor

Brown University is the lead sponsor of 282 studies on the registry; 42 are open to participants now.

Of its 25 completed or terminated interventional studies of FDA-regulated products, 18 (72%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 34 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes

Eligibility criteria

Inclusion Criteria:

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

Exclusion Criteria: Participants will be excluded from the study if they are determined to have symptoms that would prevent them from giving meaningful consent or participate in study activities including any of the following criteria:

  • Significant cognitive impairment
  • Psychosis
  • Currently symptomatic and untreated bipolar disorder
  • Imminent suicidal risk
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
68 participants (actual)

Study arms

  • Experimental
    Mindfulness-Based Queer Resilience (MBQR)

    MBQR is an online, Zoom-based mindfulness course that meets 2.5 hour per week for ten weeks, facilitated by queer mindfulness teachers, with weekly home practice and additional reflection and reading activities that can be completed by participants independently via study website portal. In addition to the 10 weekly sessions there is an all-day retreat (6hrs) that takes place around week 6. The participants also meet one-on-one with the instructor(s) at the beginning and middle of class for a 30-minute welcome call and check in.

    Behavioral: Mindfulness-Based Queer Resilience (MBQR)

  • Active comparator
    Health Education

    The online Health Education course is a self-paced program that can be largely completed independently (no group meeting, no all-day) by control group participants. The ten weekly modules are estimated to take around 30 to 90 minutes each to complete and consist of readings, videos, infographics, and other related activities (e.g., reflections, quizzes).

    Behavioral: Mindfulness-Based Queer Resilience (MBQR)

Interventions

  • BehavioralMindfulness-Based Queer Resilience (MBQR)

    This work aims to develop an internet-delivered MBI to address minority stress and its negative HIV-related health consequences experienced by young men who have sex with men (YMSM). This aim will examine the feasibility and acceptability of the internet-delivered mindfulness-based intervention (iMBI), called "Mindfulness-based Queer Resilience (MBQR)", for HIV prevention. The study will enroll and randomize a sample of 60 distressed, high-risk YMSM into one of two groups: MBQR intervention (n=30) or active control condition (n=30).

06

What researchers measure

Primary outcomes

  1. Feasibility of Online Mindfulness-Based Queer Resilience as Measured by Recruitment Rates

    The primary aim of the study is to evaluate feasibility and acceptability of Mindfulness-Based Queer Resilience. Feasibility will be assessed via three measures. One measure of feasibility will be participant recruitment rates. The recruitment rate will be calculated by comparing the total number of participants screened eligible to those who were successfully enrolled in the study. See other primary outcomes for other measures used.

    Time frame: During recruitment period of study, up to 2 months

  2. Feasibility of Online Mindfulness-Based Queer Resilience as Measured by Retention Rates: HIV/STI Testing Submission

    The primary aim of the study is to evaluate feasibility and acceptability of Mindfulness-Based Queer Resilience. Feasibility will be assessed via three measures. One measure of feasibility will be participant retention rates, as measured by number of participants completing assessments. Data for one of the three assessments (i.e., HIV/STI testing submission) is reported here. Number of participants analyzed for each timepoint represent the number of participants who submitted any of the three assessments. See other primary outcomes for other measures used.

    Time frame: Baseline, Post-intervention (week 10), and 6-month Follow-up

  3. Feasibility of Online Mindfulness-Based Queer Resilience as Measured by Retention Rates: Nail Sample Submission

    The primary aim of the study is to evaluate feasibility and acceptability of Mindfulness-Based Queer Resilience. Feasibility will be assessed via three measures. One measure of feasibility will be participant retention rates, as measured by number of participants completing assessments. Data for one of the three assessments (i.e., nail sample submission for cortisol level testing) is reported here. Number of participants analyzed for each timepoint represent the number of participants who submitted any of the three assessments. See other primary outcomes for other measures used.

    Time frame: Baseline, Post-intervention (week 10), and 6-month Follow-up

  4. Feasibility of Online Mindfulness-Based Queer Resilience as Measured by Retention Rates: Survey Submission

    The primary aim of the study is to evaluate feasibility and acceptability of Mindfulness-Based Queer Resilience. Feasibility will be assessed via three measures. One measure of feasibility will be participant retention rates, as measured by number of participants completing assessments. Data for one of the three assessments (i.e., post-intervention and 6-month follow-up survey submission) are reported here. Number of participants analyzed for each timepoint represent the number of participants who submitted any of the three assessments. See other primary outcomes for other measures used.

    Time frame: Baseline, Post-intervention (week 10), and 6-month Follow-up

  5. Feasibility of Online Mindfulness-Based Queer Resilience as Measured by Engagement

    The primary aim of the study is to evaluate feasibility and acceptability of Mindfulness-Based Queer Resilience. Feasibility will be assessed via three measures. One measure of feasibility will be engagement with the MBQR program (i.e, adherence to the prescribed intervention), which will be assessed by class attendance data. The average number of sessions that participants attended the MBQR sessions is reported here.

    Time frame: During intervention period (10 weeks)

  6. Acceptability of Online Mindfulness-Based Queer Resilience as Measured by the Client Satisfaction Questionnaire

    The primary aim of the study is to evaluate feasibility and acceptability of Mindfulness-Based Queer Resilience. Acceptability will be assessed using three measures. One such measure of acceptability will be via acceptability ratings using the validated 8-item Client Satisfaction Questionnaire (CSQ-8). Participants rated each item on a four-point Likert scale. Total scores for the CSQ-8 range from 8 to 32, with higher values indicating higher satisfaction. See other primary outcomes for other measures used.

    Time frame: Post-intervention (week 10)

  7. Acceptability of Online Mindfulness-Based Queer Resilience as Measured by a Session Evaluation Form

    The primary aim of the study is to evaluate feasibility and acceptability of Mindfulness-Based Queer Resilience. Acceptability will be assessed using three measures. One such measure of acceptability will be via a session evaluation form that provides both qualitative and quantitative feedback on the study intervention using 10 questions, rated on a four-point Likert scale, and 6 free response questions. The quantitative data is reported here. Total scores range from 10 to 40, with higher values indicating higher satisfaction. See other primary outcomes for other measures used.

    Time frame: Post-intervention (week 10)

07

Results

Posted Nov 24, 2025

Participant flow

Participant flow — Overall Study
MilestoneMindfulness-Based Queer Resilience (MBQR)Health Education
Started3434
Post-intervention assessment3433
6-month follow-up3033
Completed3033
Not completed41
Withdrew: Withdrawal by subject01
Withdrew: Lost to follow-up40

Outcome measures

PrimaryFeasibility of Online Mindfulness-Based Queer Resilience as Measured by Recruitment Rates

The primary aim of the study is to evaluate feasibility and acceptability of Mindfulness-Based Queer Resilience. Feasibility will be assessed via three measures. One measure of feasibility will be participant recruitment rates. The recruitment rate will be calculated by comparing the total number of participants screened eligible to those who were successfully enrolled in the study. See other primary outcomes for other measures used.

Time frame:
During recruitment period of study, up to 2 months
Reported as:
Count of participants · Participants
Feasibility of Online Mindfulness-Based Queer Resilience as Measured by Recruitment Rates
ParticipantsPre-randomization
Feasibility of Online Mindfulness-Based Queer Resilience as Measured by Recruitment Rates68
PrimaryFeasibility of Online Mindfulness-Based Queer Resilience as Measured by Retention Rates: HIV/STI Testing Submission

The primary aim of the study is to evaluate feasibility and acceptability of Mindfulness-Based Queer Resilience. Feasibility will be assessed via three measures. One measure of feasibility will be participant retention rates, as measured by number of participants completing assessments. Data for one of the three assessments (i.e., HIV/STI testing submission) is reported here. Number of participants analyzed for each timepoint represent the number of participants who submitted any of the three assessments. See other primary outcomes for other measures used.

Time frame:
Baseline, Post-intervention (week 10), and 6-month Follow-up
Reported as:
Count of participants · Participants
Feasibility of Online Mindfulness-Based Queer Resilience as Measured by Retention Rates: HIV/STI Testing Submission
ParticipantsMindfulness-Based Queer Resilience (MBQR)Health Education
Baseline — Completed all assessments3434
Post-intervention — Completed all assessments2629
6-month Follow-up — Completed all assessments2728
PrimaryFeasibility of Online Mindfulness-Based Queer Resilience as Measured by Retention Rates: Nail Sample Submission

The primary aim of the study is to evaluate feasibility and acceptability of Mindfulness-Based Queer Resilience. Feasibility will be assessed via three measures. One measure of feasibility will be participant retention rates, as measured by number of participants completing assessments. Data for one of the three assessments (i.e., nail sample submission for cortisol level testing) is reported here. Number of participants analyzed for each timepoint represent the number of participants who submitted any of the three assessments. See other primary outcomes for other measures used.

Time frame:
Baseline, Post-intervention (week 10), and 6-month Follow-up
Reported as:
Count of participants · Participants
Feasibility of Online Mindfulness-Based Queer Resilience as Measured by Retention Rates: Nail Sample Submission
ParticipantsMindfulness-Based Queer Resilience (MBQR)Health Education
Baseline3028
Post-intervention2326
6-month Follow-up2324
PrimaryFeasibility of Online Mindfulness-Based Queer Resilience as Measured by Retention Rates: Survey Submission

The primary aim of the study is to evaluate feasibility and acceptability of Mindfulness-Based Queer Resilience. Feasibility will be assessed via three measures. One measure of feasibility will be participant retention rates, as measured by number of participants completing assessments. Data for one of the three assessments (i.e., post-intervention and 6-month follow-up survey submission) are reported here. Number of participants analyzed for each timepoint represent the number of participants who submitted any of the three assessments. See other primary outcomes for other measures used.

Time frame:
Baseline, Post-intervention (week 10), and 6-month Follow-up
Reported as:
Count of participants · Participants
Feasibility of Online Mindfulness-Based Queer Resilience as Measured by Retention Rates: Survey Submission
ParticipantsMindfulness-Based Queer Resilience (MBQR)Health Education
Baseline3434
Post-intervention3331
6-month Follow-up2832
PrimaryFeasibility of Online Mindfulness-Based Queer Resilience as Measured by Engagement

The primary aim of the study is to evaluate feasibility and acceptability of Mindfulness-Based Queer Resilience. Feasibility will be assessed via three measures. One measure of feasibility will be engagement with the MBQR program (i.e, adherence to the prescribed intervention), which will be assessed by class attendance data. The average number of sessions that participants attended the MBQR sessions is reported here.

Time frame:
During intervention period (10 weeks)
Reported as:
Mean · Sessions
Feasibility of Online Mindfulness-Based Queer Resilience as Measured by Engagement
SessionsMindfulness-Based Queer Resilience (MBQR)Health Education
Feasibility of Online Mindfulness-Based Queer Resilience as Measured by Engagement7.18 ± 3.43—
PrimaryAcceptability of Online Mindfulness-Based Queer Resilience as Measured by the Client Satisfaction Questionnaire

The primary aim of the study is to evaluate feasibility and acceptability of Mindfulness-Based Queer Resilience. Acceptability will be assessed using three measures. One such measure of acceptability will be via acceptability ratings using the validated 8-item Client Satisfaction Questionnaire (CSQ-8). Participants rated each item on a four-point Likert scale. Total scores for the CSQ-8 range from 8 to 32, with higher values indicating higher satisfaction. See other primary outcomes for other measures used.

Time frame:
Post-intervention (week 10)
Reported as:
Mean · Scores on a scale
Acceptability of Online Mindfulness-Based Queer Resilience as Measured by the Client Satisfaction Questionnaire
Scores on a scaleMindfulness-Based Queer Resilience (MBQR)Health Education
Acceptability of Online Mindfulness-Based Queer Resilience as Measured by the Client Satisfaction Questionnaire26.61 ± 3.6018.25 ± 5.47
PrimaryAcceptability of Online Mindfulness-Based Queer Resilience as Measured by a Session Evaluation Form

The primary aim of the study is to evaluate feasibility and acceptability of Mindfulness-Based Queer Resilience. Acceptability will be assessed using three measures. One such measure of acceptability will be via a session evaluation form that provides both qualitative and quantitative feedback on the study intervention using 10 questions, rated on a four-point Likert scale, and 6 free response questions. The quantitative data is reported here. Total scores range from 10 to 40, with higher values indicating higher satisfaction. See other primary outcomes for other measures used.

Time frame:
Post-intervention (week 10)
Reported as:
Mean · Scores on a scale
Acceptability of Online Mindfulness-Based Queer Resilience as Measured by a Session Evaluation Form
Scores on a scaleMindfulness-Based Queer Resilience (MBQR)Health Education
Acceptability of Online Mindfulness-Based Queer Resilience as Measured by a Session Evaluation Form33.27 ± 4.8926.22 ± 5.92

Adverse events

Collected over From enrollment until end of follow-up, up to 6 months. Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Mindfulness-Based Queer Resilience (MBQR)0/34 (0%)0/34 (0%)0/34 (0%)
Health Education0/34 (0%)0/34 (0%)0/34 (0%)

Baseline characteristics

Age, Continuous
Age, Continuous(Years)Mindfulness-Based Queer Resilience (MBQR)Health EducationTotal
Mean27.50 ± 4.1227.15 ± 4.3027.32 ± 4.18
Sex/Gender, Customized
Sex/Gender, Customized(Participants)Mindfulness-Based Queer Resilience (MBQR)Health EducationTotal
Female000
Male293160
Gender Nonbinary, Nonconforming, Genderqueer538
Ethnicity (NIH/OMB)
Ethnicity (NIH/OMB)(Participants)Mindfulness-Based Queer Resilience (MBQR)Health EducationTotal
Hispanic or Latino12719
Not Hispanic or Latino222749
Unknown or Not Reported000
Race/Ethnicity, Customized
Race/Ethnicity, Customized(Participants)Mindfulness-Based Queer Resilience (MBQR)Health EducationTotal
Race — American Indian or Native American202
Race — Asian358
Race — Black549
Race — Multiracial268
Race — Native Hawaiian or Pacific Islander000
Race — White161430
Race — Other6511
Sexual Orientation
Sexual Orientation(Participants)Mindfulness-Based Queer Resilience (MBQR)Health EducationTotal
Gay262652
Straight000
Bisexual112
Pansexual415
Other369
08

Study locations

1 site
  • Brown University
    Providence, Rhode Island 02912, United States
09

References and documents

Study documents

  • Study protocol · Mar 31, 2023
  • Statistical analysis plan · Mar 31, 2023
  • Informed consent form · Apr 4, 2023

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: Yes — Following data collection, cleaning, and analysis, we plan to publish de-identified quantitative data at an open science data repository (e.g., Open Science Framework). De-identified qualitative data will be available upon request to the study PI.

Supporting information: Study protocol, Sap, Icf

10

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 24, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT05855655
Lead sponsor
Brown University
Collaborators
National Center for Complementary and Integrative Health (NCCIH)
Responsible party
Sponsor
First posted
May 11, 2023
Start date
Apr 8, 2023
Primary completion
Sep 30, 2024
Completion
Sep 30, 2024
Results posted
Nov 24, 2025
Last update
Nov 24, 2025

Study contacts

Shufang Sun, Ph.D.
principal investigator · Brown University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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