Effectiveness of a Peer-led Personalized Support Program Using Instant Messaging Applications and a Self-determination Theory-based Intervention to Help Young Drug Abusers Quit Drugs: A Randomized Controlled Trial
Planned date reported by the registry; this milestone is not confirmed as achieved.
Study Completion
December 31, 2026
Estimated
Planned date reported by the registry; this milestone is not confirmed as achieved.
Brief Summary
Aim: To test the effectiveness of a peer-led personalized support program using instant messaging applications and a self- determination theory-based intervention to help young drug abusers quit drugs.
Hypothesis to be tested: The investigators hypothesize that compared with those in the control group, the participants in the intervention group will experience greater success in reducing and quitting drugs and will have a better health-related quality of life at 12 months follow-up.
Registry Overview
Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.
Recruitment status
recruiting
Estimated enrollment
200 participants
Study completion date
December 31, 2026
Estimated
Planned date reported by the registry; this milestone is not confirmed as achieved.
Listed locations
1 countries · 1 sites
Trial Relationships
Click on a node to explore related trials.
Some registry-reported names shown below are not yet linked in this graph.
Related Scientific Literature
Loading related publications...
Study Timeline
Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.
First Submitted
April 13, 2023
Actual (reported)
First Posted
June 26, 2023
Actual (reported)
Study Start
June 30, 2023
Actual (reported)
Primary Completion
December 31, 2026
Estimated
Planned date reported by the registry; this milestone is not confirmed as achieved.
Study Completion
December 31, 2026
Estimated
Planned date reported by the registry; this milestone is not confirmed as achieved.
Participants' change in drug consumption between baseline and 12-month follow-up will be measured by a structured-questionnaire. The questionnaire gathers the frequency and categories of drug consumption in the past 30 days. The more frequencies and the more kinds of drug used indicating the higher consumption of drug abuse.
12 month
Secondary Outcomes (6)
The self-reported drug abuse abstinence rate
6 month and 12 month
The change in drug consumption
6 month
The changes of the contemplation stages at 6-month and 12-month
6 month and 12 month
Change of other health-related lifestyles
6 month and 12 month
The quality of life
6 month and 12 month
+1 more secondary outcomes
Study Arms (2)
Intervention group
EXPERIMENTAL
Each participant will receive the telephone that will be delivered by a trained peer supporter using the Ask, Warn, Advise, Refer and Do-it-Again (AWARD) model. For the advice steps, participants will be asked about the priority they place on engagement in health-related lifestyles. A brief intervention on the selected health-related lifestyle will be given. In addition, they will be informed that they will receive instant messaging via WeChat or WhatsApp to assist them to adhere to their schedule of the desirable health-related lifestyle throughout the study period. For the first 6 months of the study period, peer supporters will send WhatsApp or WeChat messages approximately once per week to the participants to remind them to adhere to their schedule of the desirable health-related lifestyle. In addition, the participants will receive four independent 1-minute videos which focus on the health risks associated with abusing drugs and the benefits of quitting drugs.
Other: Health-risk behaviorsOther: Theory of planned behavior, Self-determination theoryOther: Assist them to adhere to their schedule of quitting drugs throughout the study periodOther: Assist them to adhere to their schedule of desirable health-related lifestyles/quitting drugs throughout the study periodOther: (AWARD) model
Interventions
Health-risk behaviorsOther
Participants will be asked about the priority they place on engagement in health-related lifestyles, such as quitting drugs, alcohol, smoking or exercising regularly.
Intervention group
Theory of planned behavior, Self-determination theoryOther
The participants will be asked to quit drugs immediately or progressively with the ultimate goal of quitting drugs completely.
Eligibility Criteria
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Trained peer supporters will answer calls from potential participants and explain the nature and purpose of the project to them. Each participant will then receive a brief intervention over the telephone that will be delivered by a trained peer supporter using the Ask, Warn, Advise, Refer and Do-it-Again (AWARD) model. Participants will be asked to quit drugs immediately or progressively. In addition, they will be informed that they will receive instant messaging via WeChat or WhatsApp from peer supporters to assist them to adhere to their schedule of quitting drugs throughout the study period. For the first six months, participants will receive four independent 1-minute videos which focus on the health risks associated with abusing drugs and the benefits of quitting drugs without any schedule of the desirable health-related lifestyle throughout the study period.
Other: Theory of planned behavior, Self-determination theoryOther: Assist them to adhere to their schedule of quitting drugs throughout the study periodOther: (AWARD) modelOther: Receive four independent 1-minute videos
Control Group
Intervention group
Assist them to adhere to their schedule of quitting drugs throughout the study periodOther
The participants will receive instant messaging via WeChat or WhatsApp from peer supporters to assist them to adhere to their schedule of quitting drugs throughout the study period.
Control GroupIntervention group
Assist them to adhere to their schedule of desirable health-related lifestyles/quitting drugs throughout the study periodOther
The participants will receive instant messaging via WeChat or WhatsApp from peer supporters to assist them to adhere to their schedule of desirable health-related lifestyles/quitting drugs throughout the study period.
Intervention group
(AWARD) modelOther
Participants receive a brief intervention using the Ask, Warn, Advise, Refer and Do-it-Again (AWARD) model
Control GroupIntervention group
Receive four independent 1-minute videosOther
The participants will receive four independent 1-minute videos which focus on the health risks associated with abusing drugs and the benefits of quitting drugs.
Control GroupIntervention group
Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.
have an history of drug abuse within the past 12 months (including all types of drugs such as narcotics analgesics, hallucinogens, depressants, stimulants, tranquillizers and other recreational drugs)
You may not qualify if:
psychologically or physically unable to communicate
be aged 18 - 35
be able to communicate in Cantonese
have a medical background
complete the training courses and pass the evaluation of peer supporter qualification
psychologically or physically unable to communicate
Contact the study team to confirm eligibility.
Technology
Technology, Industry, and Agriculture
Television
Planned date reported by the registry; this milestone is not confirmed as achieved.
Study Completion
December 31, 2026
Estimated
Planned date reported by the registry; this milestone is not confirmed as achieved.
Last Updated
May 31, 2025
Record last verified: 2025-05
Data Sharing
IPD Sharing
Will share
The relevant anonymized patient level data, full dataset, technical appendix, and statistical code are available on reasonable request. The approval from the Principal Investigator for the purpose of data use is required.
Time Frame
After the project has been completed and the results of the project has been published
Access Criteria
Request could be sent to Principal Investigator (williamli@cuhk.edu.hk)
Source record
Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.
Source: ClinicalTrials.gov.
JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.