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NCT05145868

Just-In-Time Intervention to Reduce Alcohol-Facilitated Intimate Partner Violence Perpetration

Recruiting now NA Last updated 14 March 2025
What this trial tests

NA trial testing Alcohol Skills and Emotion Regulation Intervention in Alcohol Drinking in 400 participants. Currently enrolling.

Timeline
3 January 2023
Primary endpoint
1 April 2026
30 April 2026

Quick facts

Lead sponsorGeorgia State University
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Enrollment400
Start date3 January 2023
Primary completion1 April 2026
Estimated completion30 April 2026
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Georgia State University

Who can join

Adults 18 to 30, any sex, with Alcohol Drinking or Aggression. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Acute alcohol intoxication is a robust predictor of intimate partner violence (IPV) perpetration for young adult men and women; therefore, interventions delivered proximally to drinking episodes - a period of high risk - are needed to reduce alcohol-facilitated IPV. This project seeks to improve public health by delivering a just-in-time text messaging intervention proximally to drinking episodes and evaluating the impact of the intervention on alcohol-facilitated IPV in a sample of at-risk young adult men and women. Additionally, through an innovative design this project is poised to answer these important questions: whether receiving a message, when, for whom, what type, and under what conditions this just-in-time messaging intervention leads to reductions in alcohol use and IPV perpetration.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Alcohol Drinking

Currently open trials in the same condition.

Other Georgia State University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing