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Not yet recruiting Not applicable NCT07433270

PAIRS: Friend-Based AISA Intervention

No applicable phase (e.g. observational)
Conditions: Sexual Violence College Drinking Behavioral Changes

Sponsor: State University of New York at Buffalo

trial.available_in: БГ
Overview
This Phase 2 trial will to examine the efficacy of a brief dyad-based motivational interview (PAIRS MI) delivered to friend dyads with an active treatment-as-usual condition, and a 1-year follow-up.
Description
In this project the investigators will conduct a Phase 2 trial to test the efficacy of a friend-based motivational interview (FMI) compared to a treatment-as-usual (TAU) control, following participants over 1-year post-intervention (Aim 1.). With this trial the investigators also will address some key questions about FMI effects on target attitudes and behaviors (Aim 2.a.) that may be mechanisms of intervention outcome (Aim 2.b.). This includes Instrumental mechanisms (readiness, barriers, and assault protective behavior skills), and the dyadic relationship (closeness, collaboration between the friends in the dyad). Aim 1. In a Phase 2 trial, the investigators will examine the efficacy of a friend-based motivational intervention (FMI) to reduce AISA risk relative to an active control condition over 1-year post-intervention. The investigators will compare the FMI to a standard sexual assault prevention intervention widely used on U.S. college campuses. The investigators will use a three-level HLM, with repeated measures over one year (3, 6, 9, 12-month follow-up) nested within person (Level 2), and person nested within dyad (Level 3) to examine AISA outcomes. The investigators expect those in the FMI to report fewer incidences of AISA at follow-up assessments. Both AISA and assaults not involving alcohol will be examined. Aim 2. Examine mechanisms (instrumental, relationship) of intervention effects. In this dyad-based FMI, an interdependent process may unfold that influences outcomes whereby the FMI influences AISA risk through a person's own change, as well as through their friend's change. It is important to distinguish these two processes as each may be an important part of intervention effects. Accordingly, with longitudinal Actor-Partner Interdependence Models (APIM, Cook \& Kenny, 2005; Kenny \& Ledermann, 2017) the investigators will test whether the intervention impacts mechanisms of change through actor (a person's own change), partner (friend's change) effects, or both (Aims 2a-2c). Aim 2.a. Examine intervention effects on instrumental and relationships putative mediators, whether the putative predictors predict AISA. In this aim the investigators will test pathways relevant to the proposed mediational pathways (intervention to mediator, and mediator to outcome). Aim 2.b. Formally test actor (person's own change) mechanisms (indirect effects). Indirect effects through instrumental (readiness, FAPB skills, and perceived barriers) and relationship (closeness and collaboration) mechanisms will be tested. The investigators expect that the FMI will predict increases in closeness, collaboration, readiness, and FAPB skills, and decreases in perceived barriers, which in turn, will predict declines in AISA. Aim 2.c. Formally test partner (friend's change) mechanisms (indirect effects). Indirect effects through friend's instrumental (readiness, FAPB skills, and perceived barriers) and relationship (closeness and collaboration) mechanisms w
Who can participate
Inclusion Criteria: * Women * 4 or more drinks in a single sitting 2 or more times monthly in the past 3 months * does not live at home with parents * reports going out (not necessarily drinking) with the other member of their dyad \> 1/week Exclusion Criteria: * Can not speak and understand English sufficiently
Interventions
Friend-Based Motivational Interview
BEHAVIORAL
Treatment as usual (TAU)
BEHAVIORAL
Locations 1
United States (1)
University at Buffalo Department of Psychology
Buffalo , New York
Technical details
Status
Not yet recruiting
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Female only
Minimum age
18 Years
Maximum age
24 Years
Healthy volunteers
No
Start date
01.04.2026
Completion date
01.08.2030
Registry ID
NCT07433270
Source
clinicaltrials.gov
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