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Substance Use and Sexual Risk Reduction Intervention for Homeless Youth

15 april 2016 uppdaterad av: RAND

Brief AOD Use and Sexual Risk Reduction Group MI Intervention for Homeless

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.

Studieöversikt

Status

Avslutad

Detaljerad beskrivning

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.

Studietyp

Interventionell

Inskrivning (Faktisk)

200

Fas

  • Inte tillämpbar

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

    • California
      • Hollywood, California, Förenta staterna
        • My Friend's Place
      • Venice Beach, California, Förenta staterna, 90291
        • Safe Place for Youth

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år till 24 år (Vuxen)

Tar emot friska volontärer

Ja

Kön som är behöriga för studier

Allt

Beskrivning

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

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Förebyggande
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Ingen (Open Label)

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: 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.
Inget ingripande: Usual care control
Participant receive HIV information brochure and Community Resource Guide.

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Change in substance use
Tidsram: 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
baseline, 3 months
Change in substance use intentions
Tidsram: baseline, 3 months
Intentions to use the following in the next 3 months: alcohol; marijuana; other drugs
baseline, 3 months
Change in negative consequences from drinking
Tidsram: baseline, 3 months
baseline, 3 months
Change in use of drinking protective strategies
Tidsram: baseline, 3 months
baseline, 3 months
Change in number of different sex partners
Tidsram: baseline, 3 months
baseline, 3 months
Change in condom use
Tidsram: baseline, 3 months
baseline, 3 months
Change in substance use before or during sex
Tidsram: baseline, 3 months
baseline, 3 months
Change in HIV knowledge
Tidsram: baseline, 3 months
baseline, 3 months
Change in sex-related protective strategies
Tidsram: baseline, 3 months
baseline, 3 months
Change in sexual intentions
Tidsram: 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
baseline, 3 months
Change in HIV testing
Tidsram: baseline, 3 months
Self-report of being tested in lifetime, past 3 months
baseline, 3 months

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Sponsor

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart

1 januari 2014

Primärt slutförande (Faktisk)

1 augusti 2015

Avslutad studie (Faktisk)

1 augusti 2015

Studieregistreringsdatum

Först inskickad

10 juli 2014

Först inskickad som uppfyllde QC-kriterierna

10 juli 2014

Första postat (Uppskatta)

14 juli 2014

Uppdateringar av studier

Senaste uppdatering publicerad (Uppskatta)

19 april 2016

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

15 april 2016

Senast verifierad

1 april 2016

Mer information

Termer relaterade till denna studie

Andra studie-ID-nummer

  • R34DA034813 (U.S.S. NIH-anslag/kontrakt)

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