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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01118416
Other study ID # R01DA020366
Secondary ID
Status Completed
Phase N/A
First received May 5, 2010
Last updated May 30, 2013
Start date June 2006
Est. completion date October 2011

Study information

Verified date May 2013
Source Hunter College
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The primary aim of this study is to test a brief 4-session risk reduction intervention, based on Motivational Enhancement Therapy (MET) to reduce the co-occurrence of club drug use and sexual risk taking behaviors among non-treatment seeking young men who have sex with men (YMSM) in NYC.


Description:

This study is a randomized clinical trial. A sample of 300 non-treatment seeking YMSM (ages 18-24) who report risky sex and club drug use in the past 90 days are being enrolled using active and passive community-based recruitment strategies in NYC. After baseline assessment, participants are being randomly assigned to one of two study arms: a Brief Risk Reduction Intervention Condition - a four session MET intervention piloted for feasibility and acceptability among YMSM, designed to increase readiness to change club drug use and unprotected sex; or an Education Comparison Condition - four sessions of facilitated education regarding the effects of club drugs and unprotected sex. Participants undergo follow-up assessments 3, 6, 9, and 12 months after baseline.


Recruitment information / eligibility

Status Completed
Enrollment 317
Est. completion date October 2011
Est. primary completion date September 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 29 Years
Eligibility Inclusion Criteria:

- At least 5 days of drug use (cocaine, ketamine, ecstasy, methamphetamine, or GHB) in the past 90 days;

- At least 1 instance of unprotected anal sex in the past 90 days;

- Biological male;

- HIV-negative;

- Residential stability;

- Ability to communicate in written English.

Exclusion Criteria:

- Unstable, serious psychiatric symptoms;

- Currently suicidal/homicidal;

- Evidence of gross cognitive impairment;

- Reports current enrollment in a drug or HIV related intervention or research study.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Behavioral:
HIV prevention intervention randomized control trial
Substance using HIV-negative young MSM who engage in sexual risk are randomized to either a motivational interviewing or an education condition to reduce sexual risk and drug use.

Locations

Country Name City State
United States Center for HIV/AIDS Educational Studies and Training of Hunter College, CUNY New York New York

Sponsors (1)

Lead Sponsor Collaborator
Hunter College

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Sexual risk Participants in the MET condition will report greater reductions in the number of unprotected anal intercourse acts and in the proportion of days of club drug use than those in the education comparison condition at the end of the intervention period (3 months) and will maintain greater reductions in the number of unprotected anal intercourse acts and the proportion of days of club drug use than those in the education comparison condition at the three follow-up assessments (6, 9, and 12 months). every three months over the course of a year No
Secondary motivation to change club drug use and unsafe sex over 12 months The following factors assessed at baseline will predict club drug use and unsafe sex over the 12-month outcome period: baseline severity of club drug use, baseline severity of other substance use, motivation, decisional balance, and self-efficacy. every three months over the course of a year No
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