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OpenTrials
Active, not recruiting

NCT Number: NCT05145868

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

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.

Active, not recruiting

This study is active but is not currently recruiting participants.

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Key information

Conditions

Alcohol Drinking Aberrant Motor Behavior in Dementia Aggression Behavior Behavioral Symptoms Drinking Behavior Emotion Regulation Emotional Regulation Self-Control Social Behavior

Age range

18 year–30 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Georgia State University

Atlanta, Georgia, 30303, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18-30 years old
  • Consumed alcohol an average of 2 times per week in last 3 months
  • At least two instances of heavy episodic drinking in last month
  • Currently in a romantic relationship
  • History of IPV perpetration within last 3 months
  • Willing to provide cell phone number and carrier and receive text messages for 30 days

Exclusion criteria

  • None

Treatment and study plan

Alcohol Skills and Emotion Regulation Intervention

Behavioral

The text-based intervention will provide alcohol reduction strategies and emotion regulation skills.

Attention Control

Other

Text-messages will be sent that include no intervention content to serve as an attention control

Primary outcomes

  1. Alcohol Use

    Time frame: 30 days

    Drinking Quantity (number of drinks consumed)

  2. Alcohol Use

    Time frame: 1-month follow-up

    Drinking Quantity (number of drinks consumed)

  3. Alcohol Use

    Time frame: 3-month follow-up

    Drinking Quantity (number of drinks consumed)

  4. Alcohol Use

    Time frame: 6-month follow-up

    Drinking Quantity (number of drinks consumed)

  5. Intimate Partner Violence

    Time frame: 30 days

    Occurrence (yes/no) of psychological or physical Aggression against an intimate partner

  6. Intimate Partner Violence

    Time frame: 1-month follow-up

    Frequency of Psychological or Physical Aggression against an intimate partner

  7. Intimate Partner Violence

    Time frame: 3-month follow-up

    Frequency of Psychological or Physical Aggression against an intimate partner

  8. Intimate Partner Violence

    Time frame: 6-month follow-up

    Frequency of Psychological or Physical Aggression against an intimate partner

Sponsors and collaborators

Lead sponsor

Georgia State University

Other

Registry information

Official study title

Evaluation and Optimization of a Just-in-Time Messaging Intervention to Reduce Alcohol-Facilitated Intimate Partner Violence Perpetration Among At-Risk Young Adult Men and Women

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
Dec 6, 2021
Registry last updated
Aug 27, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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