Unsafe Sex Clinical Trial
— MLMSOfficial title:
Evaluating Locally Developed Homegrown HIV Prevention Interventions
NCT number | NCT01640392 |
Other study ID # | 1 U01SP001573-01 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | April 2012 |
Est. completion date | April 2015 |
Verified date | August 2019 |
Source | Los Angeles County Department of Public Health |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of the MyLife MyStyle Evaluation Project is to determine whether the MyLife MyStyle group-level intervention reduces HIV sexual-risk behaviors among 18- to 29-year-old African American men who have sex with men (MSM). Specifically, the project will test whether participants of the MyLife MyStyle program will report at least a 15% absolute decrease in frequency of unprotected anal sex with male partners at three and six months post-intervention compared with the wait-list control participants.
Status | Completed |
Enrollment | 528 |
Est. completion date | April 2015 |
Est. primary completion date | April 2015 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Male |
Age group | 18 Years to 29 Years |
Eligibility |
Inclusion Criteria: - Identify as African American or Black - Identify as male - Age 18 to 29 years - Reside within Los Angeles County - Self-reported anal sex with a male partner in the past 12 months - Has not participated in an HIV prevention intervention in the past 3 months - Able to complete ACASI and MyLife sessions in English Exclusion Criteria: - Identify as a transgender female - Plan to move out of Los Angeles County before the end of their follow-up period (within 7 months) |
Country | Name | City | State |
---|---|---|---|
United States | In The Meantime Men's Group, Inc. | Los Angeles | California |
Lead Sponsor | Collaborator |
---|---|
Los Angeles County Department of Public Health | Centers for Disease Control and Prevention, In The Meantime Men's Group, Inc. |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Reduced unprotected anal sex with male partners | Proportion of intervention participants reporting any unprotected anal intercourse (either insertive or receptive) with male partners at six-month follow-up (and three months for short-term effects) compared with those in the wait-list control arm. | up to 6 months following Intervention groups' third (final) session | |
Secondary | Increased communication with partners | Increase frequency of communication with partner(s) about safer sex, HIV status, STI status | 3 months and 6 months following intervention groups' third (final) session | |
Secondary | Decrease unprotected sex because condom was not available | Proportion of intervention participants reporting episodes of unprotected anal sex when a condom is not available at six-month follow-up (and three months for short-term effects) compared with those in the wait-list control arm. | 3 months and 6 months following Intervention groups' third (final) session | |
Secondary | Decrease number of sexual partners | Number of sexual partners reported by intervention participants at six-month follow-up (and three months for short-term effects) compared with the number reported by the wait-list control participants. | 3 months and 6 months following Intervention groups' third (final) session | |
Secondary | Increase help-seeking behaviors for sexual health, e.g., STI testing, HIV testing, health screenings | Proportion of intervention participants reporting help-seeking behaviors for sexual health at six-month follow-up (and three months for short-term effects) compared with those in the wait-list control arm. | 3 months and 6 months following Intervention groups' third (final) session |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT01907126 -
HIV/STI Risk Reduction for Incarcerated Women With Interpersonal Violence
|
Phase 2 | |
Completed |
NCT03980873 -
Cognitive-Behavioral Therapy for Young Adult Lesbian, Gay and Bisexual: Transdiagnostic Minority Stress Approach
|
N/A | |
Completed |
NCT02387489 -
A Clinical Trial of SBIRT Services in School-based Health Centers
|
N/A | |
Completed |
NCT01849029 -
Cognitive Processing Intervention for Trauma, HIV/STI Risks, and Substance Use Among Native Women
|
N/A | |
Completed |
NCT01499706 -
Telephone-delivered Behavioral Interventions to Reduce Risky Sexual Behavior in HIV-positive Late Middle-age and Older Adults
|
Phase 1 | |
Completed |
NCT01351389 -
Brief Interventions in the Emergency Department for Alcohol and HIV/Sexual Risk
|
N/A | |
Recruiting |
NCT03224416 -
Individual and Contextual Factors That Influence Sexual Decisions
|
N/A | |
Not yet recruiting |
NCT06435234 -
Construction of a Risky Sexual Behaviour Intervention Programme for College Students Based on BCW Theory
|
N/A | |
Completed |
NCT01690494 -
Protect and Connect: Couple HIV Prevention for Drug Involved Male Offenders
|
N/A | |
Completed |
NCT03637322 -
Evaluation of Implementation of the Phoenix PrEP (Pre-Exposure Prophylaxis) Access Project for Youth Aged 13-24
|
||
Completed |
NCT01376895 -
Project Power: An HIV Risk Reduction Intervention for Black Men Who Have Sex With Men and Women (BMSM/W)
|
Phase 1/Phase 2 | |
Active, not recruiting |
NCT04597424 -
Combined Prevention of Sexually Transmitted Infections (STIs) in Men Who Have Sex With Men and Using Oral Tenofovir Disoproxil Fumarate/ Emtricitabine (TDF/FTC) for HIV Pre-Exposure Prophylaxis (PrEP)
|
Phase 3 | |
Completed |
NCT02847858 -
Health-E You: Reducing Unintended Pregnancies Among Hispanic Adolescents
|
N/A | |
Completed |
NCT03961633 -
AWARE Intervention: Feasibility and Efficacy Trial at Three University Health Services Centers
|
N/A |