Mode
Text Size
Log in / Sign up
N/A N=30 Treatment

Social Support Intervention for Addiction Recovery

Alcohol; Harmful Use · Alcohol

Enrolled (actual)
30
Serious AEs
0.0%
Results posted
Nov 2025
Primary outcome: Primary: Recruitment Feasibility — 10 participants per month

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
LDART (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Yale University
Primary completion
Jul 2024

Outcome Measures

OutcomeResultp-value
PRIMARY
Recruitment Feasibility
10
PRIMARY
Retention Feasibility
23
PRIMARY
Intervention Acceptability (Engagement With Intervention)
22.9
PRIMARY
Intervention Acceptability (Subjective Experience)
18
SECONDARY
Percentage of Drinking Days Per Month
61.3; 45.2; 42.6
SECONDARY
Percentage of Heavy Drinking Days Per Month
27.1; 17.1; 17.9
SECONDARY
Hours Spent Engaging With Recovery Support Services
2.4; 10.8; 7.6
SECONDARY
World Health Organization Quality of Life - Brief Version
57.1; 60.7; 60.1
SECONDARY
Brief Assessment of Recovery Capital
43.9; 46.9; 45.3

Summary

The purpose of this research study is to determine whether using a web-based intervention is feasible, acceptable, and helpful for people who engage in hazardous alcohol use and want to cut down or quit.

Eligibility Criteria

Inclusion Criteria

  • 18 years of age or older
  • Is at the time of study participation residing in Connecticut, USA
  • Is fluent in English and has a 6th grade reading level or higher
  • Alcohol Use Disorders Identification Test (AUDIT) score of ≥8
  • Has had at least one heavy drinking day in the past month
  • Has some desire to cut down or quit their alcohol use
  • Has a smartphone or computer with access to internet

Exclusion Criteria

  • Has vulnerable population status (e.g., pregnant people, prisoners)
  • Is at the time of study participation receiving in-patient psychiatric treatment involving hospitalization
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT06022107). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search