Alcohol Brief Intervention Plus Personalized Mobile Chat-based Intervention to Reduce Alcohol Misuse in an Emergency Department
A Pilot Study on the Feasibility of Alcohol Brief Intervention Plus Personalized Mobile Chat-based Intervention to Reduce Alcohol Misuse in an Emergency Department in Hong Kong
1 other identifier
interventional
20
1 country
1
Brief Summary
This project focuses on patients in AED. Objectives of this project are:
- 1.To examine the factors associated with alcohol drinking and alcohol use disorder
- 2.To examine the effect of face-to-face alcohol brief intervention on drinking reduction
- 3.To examine the effect of a continuous interactive chat-based intervention via "WhatsApp" on drinking reduction
- 4.To explore the perception of face-to-face alcohol brief intervention
- 5.To explore the perception of continuous interactive chat-based intervention via instant messaging mobile application "WhatsApp"
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Feb 2019
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 27, 2019
CompletedFirst Posted
Study publicly available on registry
January 30, 2019
CompletedStudy Start
First participant enrolled
February 1, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 30, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
May 30, 2019
CompletedSeptember 26, 2019
September 1, 2019
3 months
January 27, 2019
September 24, 2019
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
change in unit of alcohol consumption in gram
Assessed by unit in gram and compare the alcohol consumption between intervention and control group at 3-month after baseline.
at 3-month after baseline.
Secondary Outcomes (6)
change in unit of alcohol consumption in gram
at 1-month after phase I
change in episode of binge drinking measured by asking "Never", "less than a month", "two to four times a month", " two to three times a week" and "almost everyday"
at 1 and 3 months after phase I
change in frequency of drinking by asking "Never", "less than a month", "two to four times a month", " two to three times a week" and "almost everyday"
at 1 and 3 months after phase I
attempt to reduce drinking measured by asking whether they have tried to reduce drinking at past month (yes or no)
at 1 and 3 months after phase I
change in confidence to reduce drinking measured by Likert scale (1-10)
at 1 and 3 months after phase I
- +1 more secondary outcomes
Study Arms (2)
Intervention group
EXPERIMENTALAlcohol brief intervention+mobile chat-based instant messages
control group
ACTIVE COMPARATORAlcohol brief intervention
Interventions
Subjects in the active arm study will receive 5-minute face-to-face ABI, alcohol leaflet from Department of Health (DH) plus continuous interactive chat-based intervention for 1 month as an extension of alcohol brief intervention at baseline
The Control group will receive face-to-face ABI plus an alcohol leaflet from DH.
Eligibility Criteria
You may qualify if:
- Hong Kong resident aged 18 to 65
- scored ≥ 8 in the Alcohol Use Disorder Identification Test (AUDIT) in the past 12 months
- able to communicate in Cantonese (including reading Chinese)
- using a phone with instant messaging mobile application "WhatsApp" installed for communication.
You may not qualify if:
- patients with communication barrier (either physically or cognitively)
- currently participating in other alcohol treatment services or clinics
- will be hospitalized immediate after A\&E consultation
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- The University of Hong Konglead
- Queen Mary Hospital, Hong Kongcollaborator
Study Sites (1)
School of Nursing, The University of Hong Kong
Hong Kong, 000000, Hong Kong
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Man Ping Wang, PhD
The University of Hong Kong
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
January 27, 2019
First Posted
January 30, 2019
Study Start
February 1, 2019
Primary Completion
April 30, 2019
Study Completion
May 30, 2019
Last Updated
September 26, 2019
Record last verified: 2019-09