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Completed

NCT Number: NCT03823599

Alcohol Brief Intervention Plus Personalized Mobile Chat-based Intervention to Reduce Alcohol Misuse in an Emergency Department

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"

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

School of Nursing, The University of Hong Kong

Hong Kong, 000000

About this study

According to the Department of Health, a local epidemiological study was conducted in 2001 and showed that about one in ten of all motor vehicle deaths were associated with alcohol consumption. Also, the statistics from the Transportation department showed that 874 vehicle accidents resulting in personal injury were related to alcohol misuse, which included 24 fatal cases between the period of 2000 and 2010. With the aforementioned statistics supported, the hospital Accident and Emergency Department (AED) serves as the most important entrance and safeguard to the healthcare system for the public, since victims of traffic accidents or violence related to heavy drinking are frequently encountered in AED, this serves as an ideal place for provision of initial alcohol intervention and further stabilization related to alcohol problem of patients. Although AED is a hectic environment with very high patients turnover, substantial evidence had shown feasibility and efficacy of Alcohol Brief Intervention (ABI) in reducing patients' subsequent alcohol drinking. In oversea, multiple research had been done to show ABI were effective and feasible for reducing alcohol misuse, but the effect was not long lasting and lead to subsequent relapse. In addition to this, no further trial has been done to investigate the feasibility of implementing an RCT on evaluating the effect of ABI and continuous chat-based intervention on reducing alcohol consumption among patients in AED in Hong Kong.

According to the WHO, the standard ABI approach includes: giving feedback and information about the screening result and hazard of drinking; emphasizing the benefits of quit drinking and informing about alcohol problems; setting goal on reducing alcohol consumption; reviewing advice and ; giving encouragement. In this pilot study, a brief alcohol counselling using face-to-face ABI will be delivered together with continuous interactive chat-based intervention via instant messaging mobile application "WhatsApp" to those patients with AUDIT score ≥ 8, who are considered to have hazardous and harmful drinking problems according to the guideline.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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.

Exclusion criteria

  • 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

Treatment and study plan

Mobile chat-based instant messages

Behavioral

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

Alcohol brief intervention

Behavioral

The Control group will receive face-to-face ABI plus an alcohol leaflet from DH.

Primary outcomes

  1. change in unit of alcohol consumption in gram

    Time frame: at 3-month after baseline.

    Assessed by unit in gram and compare the alcohol consumption between intervention and control group at 3-month after baseline.

Secondary outcomes

  1. change in unit of alcohol consumption in gram

    Time frame: at 1-month after phase I

    Assessed by unit in gram and compare the alcohol consumption between intervention and control group at 1-month after phase I

  2. 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"

    Time frame: at 1 and 3 months after phase I

    Defined by 5 [male] or 4 [female] in a row for binge drinking and compare the episode of binge drinking between intervention group and control at baseline, 1 and 3-month follow-up questionnaires

  3. 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"

    Time frame: at 1 and 3 months after phase I

    Compare the frequency of drinking between intervention group and control at baseline, 1 and 3-month follow-up questionnaires

  4. attempt to reduce drinking measured by asking whether they have tried to reduce drinking at past month (yes or no)

    Time frame: at 1 and 3 months after phase I

    Compare the attempt to reduce drinking between intervention group and control group at baseline, 1 and 3-month follow-up questionnaires

  5. change in confidence to reduce drinking measured by Likert scale (1-10)

    Time frame: at 1 and 3 months after phase I

    Score ranges from 0 to 10 with higher score indicates a high level. The score will be compared between intervention group and control group at baseline, 1 and 3-month follow-up questionnaires

  6. Alcohol Problems Scale at 1 and 3-month follow-up

    Time frame: at 1 and 3 months after phase I

    The 14-item measure of alcohol-related personal, social, sexual, and legal problems (eg, being physically aggressive toward someone while under the influence of alcohol).The score will be compared between intervention group and control group at baseline, 1 and 3-month follow-up questionnaires

Sponsors and collaborators

Lead sponsor

The University of Hong Kong

Other

Collaborators

  • Queen Mary Hospital, Hong Kong

Registry information

Official study title

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

Important dates

Study start
2019
Primary completion
2019
Study completion
2019
First posted
Jan 30, 2019
Registry last updated
Sep 26, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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