Brief Mobile Intervention for Prepartying

Sponsor
RAND (Other)
Overall Status
Recruiting
CT.gov ID
NCT04016766
Collaborator
University of Southern California (Other)
500
1
2
12.7
39.3

Study Details

Study Description

Brief Summary

The primary objective of the research study is to develop and test a prepartying (aka "pregaming") specific brief mobile app intervention that is intended to help college students reduce their prepartying drinking behavior. Such behavior has been identified as a major contributor to alcohol-related negative consequences among young people. The investigators will first develop the intervention content based on theory and research supporting mechanisms of change in brief interventions with college students and document normative drinking information from 500 college students for inclusion in the intervention content. Investigators will then beta test the intervention with a sample of 14 heavy drinking college students. Focus group feasibility and acceptability feedback will inform the final intervention content. Investigators will then pilot test the mobile-based intervention in a randomized controlled trial of 500 college students who preparty frequently (n = 250 intervention, n = 250 attention control) and determine the efficacy of the intervention on (1) preventing heavy consumption levels during and after prepartying and on (2) reducing students' global levels of heavy drinking and consequences one and three months post-intervention.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Mobile app prepartying intervention
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
500 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Mobile Application Intervention Targeting the High Risk Drinking Practice of Prepartying
Actual Study Start Date :
Aug 9, 2021
Anticipated Primary Completion Date :
May 31, 2022
Anticipated Study Completion Date :
Aug 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Prepartying mobile app intervention

Mobile app intervention

Behavioral: Mobile app prepartying intervention
The intervention is comprised of a theoretically-informed and empirically-supported, brief, accessible, and personalized intervention to address prepartying drinking. the prepartying intervention app will be tailored toward an individual's personal goals, beliefs (perceptions, expectancies, self-efficacy), and behavior (protective strategies), and focus on the core components of brief interventions that have been cited as constructs that mediate the effects of multiple component intervention programs (e.g., correcting perceived norms, use of protective behavioral strategies, increased self-efficacy, challenging expectancies, feedback on blood alcohol level).

No Intervention: Control

Control participants receive a personalized attention control task (i.e., listing and ranking favorite movies, music, and books), which controls for the time needed by the intervention group to view the intervention material.

Outcome Measures

Primary Outcome Measures

  1. Prepartying frequency [Past month (30 days)]

    Number of days reported prepartying on the timeline followback

  2. Drinks during prepartying [Past month (30 days)]

    Average number of drinks reported during prepartying on the timeline followback

  3. Drinking frequency [Past month (30 days)]

    Number of days reported any drinking on the timeline followback

  4. Drinks on drinking days [Past month (30 days)]

    Average number of drinks reported during drinking days on the timeline followback

  5. 21-item Brief Young Adult Alcohol Consequences Questionnaire [Past month (30 days)]

    Number of 21 assessed alcohol consequences experienced (yes/no). Yes responses are summed to yield a score on this measure. Higher scores indicate experience of a greater number of consequences. Scores range from 0 (no consequences) to 21 (experience of all 21 consequences)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 24 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • full time undergraduate college student

  • between the ages of 18 and 24

  • report typically prepartying at least once per week

Exclusion Criteria:
  • not meeting inclusion criteria

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Southern California Los Angeles California United States 90089

Sponsors and Collaborators

  • RAND
  • University of Southern California

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
RAND
ClinicalTrials.gov Identifier:
NCT04016766
Other Study ID Numbers:
  • R34AA025968
First Posted:
Jul 11, 2019
Last Update Posted:
Aug 17, 2021
Last Verified:
Aug 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Aug 17, 2021