Substance Use and Sexual Risk Reduction Intervention for Homeless Youth

Sponsor
RAND (Other)
Overall Status
Completed
CT.gov ID
NCT02188797
Collaborator
(none)
200
2
2
19
100
5.3

Study Details

Study Description

Brief Summary

The goal of this study is to evaluate a group-based motivational interviewing (MI)-delivered risk reduction program for homeless young adults. It is hypothesized that youth who participate in the program will show greater reductions in substance use intentions, behavior and consequences, as well as sexual activity intentions and risk behavior, over a 3-month period compared to a usual care control sample of youth who do not participate in the program.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Group MI risk reduction program
N/A

Detailed Description

This study addresses an important gap in prevention services for homeless youth by conducting a pilot test of an innovative 4-session integrated substance use and sexual risk reduction program for this population that is feasible to deliver in settings where these youth seek services. The study has 2 specific aims:

Aim 1: Investigate whether homeless youth who participate in the program show reductions in substance use and intentions, behavior and consequences, as well as sexual activity intentions and risk behavior, over a 3-month period compared to a usual care control sample of youth who do not receive the program.

Aim 2: Gain a better understanding of intervention effects by exploring whether improvements in self-efficacy, readiness to change, outcome expectancies, and exposure to peer substance use and offers serve as explanatory mechanisms for reductions in substance use- and sexual activity- related intentions and risk behaviors among youth who participate in the program.

The program will be evaluated using a form of group-randomized design, although with crossover of conditions and groups to avoid the problems of power reduction associated with conventional group randomization. The unit of analysis will be the individual, but individuals will be assigned to groups based on the agency where they are seeking services. Youth at two drop-in centers serving homeless youth will either be in the intervention condition or a "usual care" control condition. The field period will be divided into four phases. The two agencies will alternate across phases in serving as the "intervention site" or "control site," with each agency having a total of two intervention phases and two control phases.

Intervention Condition: This condition involves a four-session voluntary intervention that is delivered within a drop-in center setting and is based on the investigator's previous intervention work with adolescents and young adults. Each session lasts approximately 1 hour. The intervention focuses on both sexual risk behavior and substance use. Although some sessions focus more heavily on sexual risk and others on substance use, each session includes content that emphasizes the interrelated nature of these two risk behaviors. In all sessions, participants will receive a personalized feedback sheet that specifically addresses a topic being discussed during that particular session. An motivational interviewing approach will be used to present material during the group sessions.

"Usual Care" Condition: The "usual care" condition reflects the resources typically available in settings that serve homeless youth: an HIV informational brochure that discusses the connection between substance use and HIV risk, and a Community Resource Guide that lists free or low-cost substance use and HIV-related services.

Study Design

Study Type:
Interventional
Actual Enrollment :
200 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Brief AOD Use and Sexual Risk Reduction Group MI Intervention for Homeless
Study Start Date :
Jan 1, 2014
Actual Primary Completion Date :
Aug 1, 2015
Actual Study Completion Date :
Aug 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Experimental: Group MI risk reduction program

Participants receive four 1-hour group motivational interviewing sessions focused on reducing substance use and sexual risk behavior. They also receive an HIV information brochure and Community Resource Guide.

Behavioral: Group MI risk reduction program

No Intervention: Usual care control

Participant receive HIV information brochure and Community Resource Guide.

Outcome Measures

Primary Outcome Measures

  1. Change in substance use [baseline, 3 months]

    past month quantity-frequency of alcohol and marijuana; past 3 months frequency of alcohol, binge drinking, marijuana, crack, cocaine, heroin, methamphetamine, ecstasy, hallucinogens, inhalants, prescription drug misuse

  2. Change in substance use intentions [baseline, 3 months]

    Intentions to use the following in the next 3 months: alcohol; marijuana; other drugs

  3. Change in negative consequences from drinking [baseline, 3 months]

  4. Change in use of drinking protective strategies [baseline, 3 months]

  5. Change in number of different sex partners [baseline, 3 months]

  6. Change in condom use [baseline, 3 months]

  7. Change in substance use before or during sex [baseline, 3 months]

  8. Change in HIV knowledge [baseline, 3 months]

  9. Change in sex-related protective strategies [baseline, 3 months]

  10. Change in sexual intentions [baseline, 3 months]

    Separate items for intentions for buying/getting condoms, carrying condoms, talking to partner about condoms, using condoms, using condoms when drinking or using drugs, getting tested

  11. Change in HIV testing [baseline, 3 months]

    Self-report of being tested in lifetime, past 3 months

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 24 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • between 18-24 years, receiving services at one of the participating drop-in centers, planning to be in the study area for the next month
Exclusion Criteria:
  • obvious cognitive impairment observed during screening process; non-English speaking

Contacts and Locations

Locations

Site City State Country Postal Code
1 My Friend's Place Hollywood California United States
2 Safe Place for Youth Venice Beach California United States 90291

Sponsors and Collaborators

  • RAND

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
RAND
ClinicalTrials.gov Identifier:
NCT02188797
Other Study ID Numbers:
  • R34DA034813
First Posted:
Jul 14, 2014
Last Update Posted:
Apr 19, 2016
Last Verified:
Apr 1, 2016

Study Results

No Results Posted as of Apr 19, 2016