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N/A Completed N=398 Randomized Supportive Care

Family-focused vs. Drinker-focused Smartphone Interventions to Reduce Drinking-related Consequences of COVID-19

Alcohol Use Disorder · Family Members · Behavior, Addictive
Source: ClinicalTrials.gov NCT05419128 ↗
Enrolled (actual)
398
Serious AEs
0.0%
Results posted
May 2025
Primary outcomePrimary: % of Patient Risky Drinking Days — 27.53; 18.58; 15.44; 28.12 percentage of high-risk drinking days

Summary

This R01 project titled "Family-focused vs. Drinker-focused Smartphone Interventions to Reduce Drinking-related Consequences of COVID-19" is a Hybrid II RCT/implementation study to modify and test two of our alcohol smartphone interventions to address the fallout from COVID. We propose a three-arm RCT comparing a smartphone control group vs. a drinker-focused intervention vs. a family-focused intervention. All study arms recruit dyads comprising a person who drinks and a family partner.

Outcome Measures

OutcomeResultp-value
PRIMARY
% of Patient Risky Drinking Days
53.99; 48.78; 43.43; 27.98; 30.52; 28.43
SECONDARY
Psychological Distress
69.77; 71.97; 70.35; 51.16; 48.36; 52.84
SECONDARY
% Days Abstinent
27.59; 28.79; 38.59; 58.25; 50.07; 60.30
SECONDARY
Relationship Satisfaction
22.87; 22.09; 22.73; 21.65; 22.86; 23.24

Eligibility Criteria

Inclusion Criteria

  • Identified patients and their concerned significant others must give informed consent; agree to complete interviews at baseline, 4, 8, and 12 months; and not have a mental or physical condition that limits smartphone use. Identified patients must be age 18 or older and meet criteria for risky drinking (for men, >4 standard drinks in a day; for women, >3 in a day), or meet criteria for AUD (any severity) defined by DSM-5 and have had at least 1 drink in the past 3 months . Partner must be a committed romantic partner/spouse, close friend or family member (e.g. sibling, parent, grandparent, adult child age 21 or older).

Exclusion Criteria

  • Individuals were not eligible if they had current (last 6 months) evidence of serious mental illness (eg, active psychosis, active manic phase), or if either partner reported serious interpersonal violence, to avoid risk of violence from engagement on potentially sensitive subjects.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05419128). 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. Informational only — not medical advice.

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