Skip to main content
Clinical Trials/NCT03589508
NCT03589508
Completed
N/A

Testing A Couple-based Program for Alcohol Risk Reduction in the National Guard

University of Massachusetts, Worcester1 site in 1 country44 target enrollmentJuly 1, 2016

Overview

Phase
N/A
Intervention
Not specified
Conditions
Alcohol; Harmful Use
Sponsor
University of Massachusetts, Worcester
Enrollment
44
Locations
1
Primary Endpoint
Attitude Items
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The purpose of this project is to develop and test indicated prevention intervention to harness support and health promoting endeavors to address use of alcohol to cope with reintegration challenges in Massachusetts National Guard (MANG) service members.

Detailed Description

Specific Aim 1: To modify the existing, efficacious Alcohol Behavioral Couple Therapy (ABCT) manual into a 6-session prevention protocol, called Alcohol Behavioral Couple Prevention (ABCP) that will be developed for delivery via in-person and telehealth platforms. The goal of the new ABCP is for individuals or family dyads to learn to work together to minimize hazardous drinking in order to effectively address other problems often present among returning service members. Specific Aim 2: To field test feasibility and preliminary efficacy of a prevention protocol using a successive cohort design. First, an in-person protocol will be tested with 4 National Guard (NG) members and then adapt and test the protocol for 4 NG members via an analog telehealth design. Again, the manual and accompanied materials will be revised. Specific Aim 3: To conduct a small Randomized Controlled Trial (RCT) to compare 2 conditions with 22 NG Members in each: (1) In person (ABCP_P; 11 individual, 11 dyad), and (2) Telehealth (ABCP_T; 11 individual, 11 dyad).

Registry
clinicaltrials.gov
Start Date
July 1, 2016
End Date
March 25, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University of Massachusetts, Worcester
Responsible Party
Principal Investigator
Principal Investigator

Elizabeth Epstein

Professor

University of Massachusetts, Worcester

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • unable to give consent
  • Prisoners
  • Principal Investigators determined the participant requires a higher level of care (based on unstabilized psychiatric disorder, and/or high drinking or drug use severity, and/or inability to attend to adl's and/or agitated behavior
  • Service Member is unable to read or comprehend English at the 7th grade education level

Outcomes

Primary Outcomes

Attitude Items

Time Frame: Baseline and through study completion, about 8 weeks

6 item self-report questionnaire assessing attitudes toward drinking under different circumstances. Item scores were summed to calculate total scores, with scores ranging from 6 to 24. Higher scores indicate greater attitudes about acceptability of drinking across situations.

Percent Drinking Days

Time Frame: Change from baseline at 2 months post session 1

Derived from Timeline Followback (TLFB)

Percent Heavy Drinking Days

Time Frame: Change from baseline at 2 months post session 1

Derived from Timeline Followback (TLFB)

Mean Drinks Per Drinking Day

Time Frame: Change from baseline at 2 months post session 1

Derived from Timeline Followback (TLFB)

Secondary Outcomes

  • Coping Strategies Scale(Change from baseline at 2 months post Session 1)
  • Alcohol Expectancies Questionnaire 3(Change from baseline at 2 months post Session 1)
  • Treatment Services Review(Weekly for up to 8 weeks)
  • Couple Satisfaction Inventory 16(Baseline and through study completion, about 8 weeks)
  • Perceived Social Support - Family(Baseline and through study completion, about 8 weeks)
  • Outcomes Questionnaire (OQ) - 30(Baseline and through study completion, about 8 weeks)
  • Working Alliance Inventory Short Form(Baseline and through study completion, about 8 weeks)
  • Use of Prevention Skills(Baseline and through study completion, about 8 weeks)
  • Copello Coping Questionnaire(Baseline and through study completion, about 8 weeks)
  • World Health Organization Quality of Life (WHOQOL) Questionnaire - Bref(Change from baseline at 2 months post Session 1)

Study Sites (1)

Loading locations...

Similar Trials