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Clinical Trials/NCT07381868
NCT07381868RecruitingNot Applicable

Social Media Psychosocial Support Group to Reduce Alcohol Consumption in Women: a Pilot Randomized Controlled Trial

The University of Hong Kong1 site in 1 country60 target enrollmentStarted: May 1, 2026Last updated:
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
60
Locations
1
Primary Endpoint
Alcohol use

Study Overview

Brief Summary

This proposed study aims to develop and examine the feasibility, acceptability, and preliminary effectiveness of a proactive intervention model that combines brief psychological counselling, Ecological Momentary Assessment (EMA) and social media psychosocial support group to reduce alcohol consumption in women.

Detailed Description

Targeted participants are adult women with a total a total score≥3 in Alcohol Use Disorders Identification Test - Consumption (AUDIT-C). Sixty participants will be actively recruited from the social media platform in Hong Kong.

This study will be a two-arm (allocation ratio:1:1; permutated block size of 2, 4, and 8), single blinded, parallel, pilot randomized controlled trial (RCT) with follow-ups at 4, 8, and 12 weeks post-enrollment using consolidated standards of reporting (CONSORT) to evaluate the effectiveness of the intervention. The control group will receive an evidence-based intervention composed of brief psychological counselling and health education, 4-week EMA and social media psychosocial support group, guided by comprehensive assessment. Surveys will be collected via telephone. Semi-structured individual telephone or face-to-face indepth interviews will be conducted with the participants in the intervention group to understand the experience and the perceptions towards the EMA data collection and ocial media psychosocial support group intervention on alcohol consumption.

The clinical outcome of this study will be the difference in the alcohol consumption, anxiety and depressive levels, stress levels, and family well-being between the two groups at 4, 8, and 12 weeks.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Health Services Research
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Adult women (age 18+),
  • Had a total score ≥3 in AUDIT-C [suggesting at-risk drinkers (i.e., binge drinking)]( potential distress symptoms),
  • Able to read and understand Chinese and use an instant messaging app weekly

Exclusion Criteria

  • Women who are undergoing psychiatric/psychological treatment

Arms & Interventions

Conrtol group

Active Comparator

Participatns in the control group will receive alcohol brief intervention according to their AUDIT score at baseline and 4 weeks 1-to-1 health education messages.

Intervention: Brief alcohol use counselling and health education (Behavioral)

Intervention group

Experimental

A 4-week psychological support group for interactive counselling will be provided to encourage reducing alcohol consumption. MHealth messages will also be provided according to the stages of change for alcohol use.

Intervention: mHealth-based motivational counselling (Behavioral)

Intervention group

Experimental

A 4-week psychological support group for interactive counselling will be provided to encourage reducing alcohol consumption. MHealth messages will also be provided according to the stages of change for alcohol use.

Intervention: Brief alcohol use counselling and health education (Behavioral)

Intervention group

Experimental

A 4-week psychological support group for interactive counselling will be provided to encourage reducing alcohol consumption. MHealth messages will also be provided according to the stages of change for alcohol use.

Intervention: Social media group support with engagement management (Behavioral)

Outcomes

Primary Outcomes

Alcohol use

Time Frame: 4-, 8-, and 12-weeks after enrollment

Alcohol use is measured by the Alcohol Use Disorders Identification Test (AUDIT) scale. It is a standardized, 10-item self-report screening instrument developed by the World Health Organization (WHO) to identify hazardous alcohol consumption, harmful drinking behaviors, and alcohol use disorders (AUDs). Respondents rate each item on a 5-point Likert scale (0 = never to 4 = daily or almost daily), with total scores ranging from 0 to 40. The higher the score, the greater the risk of individual alcohol abuse and dependence. Established cutoff values guide interpretation: Scores 0-7: Generally indicates low-risk or abstinence. Scores 8-14: Suggests hazardous or harmful alcohol use. Scores 15-19: Indicates a high level of harmful alcohol use. Simple advice and periodic review are advised. Scores 20-40: Suggests a likely alcohol dependence syndrome and the need for further diagnostic evaluation and specialist treatment consideration.

Secondary Outcomes

  • Anxiety(4-, 8-, and 12-weeks after enrollment)
  • Depressive symptoms(4-, 8-, and 12-weeks after enrollment)
  • Stress(4-, 8-, and 12-weeks after enrollment)
  • Perceived family well-being(4-, 8-, and 12-weeks after enrollment)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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