N/A
N=356
Peer Online Motivational Interviewing for Sexual and Gender Minority Male Survivors
Sexual Abuse
Bottom Line
View on ClinicalTrials.gov: NCT03794986 ↗Enrolled (actual)
356
Serious AEs
0.6%
Results posted
Apr 2024
Primary outcome: Primary: Number of Participants Who Engage in Mental Health Treatment — 23; 18; 31; 26 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Trauma-informed SGM affirmative care (Behavioral); Motivational Interviewing (Behavioral)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- Male
- Sponsor
- Yale University
- Primary completion
- Nov 2021
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number of Participants Who Engage in Mental Health Treatment |
23; 18; 31; 26; 28; 31 | — |
| PRIMARY Center for Epidemiological Studies Depression Scale |
30.50; 30.70; 24.04; 22.87; 27.33; 25.46 | — |
| SECONDARY Post Traumatic Stress Disorder |
36.26; 36.45; 29.30; 27.84; 32.22; 29.21 | — |
| SECONDARY Psychosocial Functioning |
45.64; 44.71; 39.88; 38.51; 39.97; 34.05 | — |
| SECONDARY Substance Abuse |
4.92; 4.75; 7.71; 8.26; 5.89; 5.69 | — |
| SECONDARY Substance Abuse |
4.92; 4.75; 7.71; 8.26; 5.89; 5.69 | — |
Summary
The study will conduct a randomized comparative effectiveness trial of peer-facilitated, online, 6-week group Motivational Interviewing (MI) vs. Motivational Interviewing (MI) with a trauma-informed Sexual and Gender Minority (SGM) affirmative care approach.
Eligibility Criteria
Inclusion Criteria
- 18 years or older
- English-speaking; men who have sex with men or individuals identifying as SGM males
- Individuals who report a history of sexual abuse and individuals who self-report a minimum cut-off score of 3.0 or higher on emotional distress, using a 4-question symptom inventory.
Exclusion Criteria
- Individuals who endorse active psychosis
- Individuals who have a cognitive dysfunction
- SGM men who report that they are currently in formal mental health counseling
Data sourced from ClinicalTrials.gov (NCT03794986). 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.