NCT04634968

Brief Summary

A pilot randomized control trial will be conducted attaching to the MedPAC services to evaluate the feasibility and acceptability of a Motivational Interviewing (BMI) interaction via instant messaging apps on reducing the drug abuse among youth in Hong Kong.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
20

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Nov 2020

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

November 9, 2020

Completed
6 days until next milestone

Study Start

First participant enrolled

November 15, 2020

Completed
3 days until next milestone

First Posted

Study publicly available on registry

November 18, 2020

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 15, 2021

Completed
7 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 4, 2021

Completed
Last Updated

July 28, 2022

Status Verified

October 1, 2021

Enrollment Period

6 months

First QC Date

November 9, 2020

Last Update Submit

July 27, 2022

Conditions

Keywords

drug abusebrief motivational interviewpeer counsellinginstant messagingadolescent

Outcome Measures

Primary Outcomes (1)

  • Changes of drug abuse consumption

    The participants' changes of drug abuse consumption between baseline and 1-month follow-up.

    1-month

Secondary Outcomes (11)

  • Changes of level of readiness to quit

    1-month

  • The rate of changes of level of readiness to quit at 3 month comparing to that at baseline

    3-month

  • The rate of changes of level of readiness to quit at 6 month comparing to that at baseline

    6-month

  • Changes of perceived treatment needs

    1-month

  • Changes of perceived treatment needs

    3-month

  • +6 more secondary outcomes

Study Arms (2)

intervention group

EXPERIMENTAL

The interactive Brief MI-based text message communication via instant messaging apps (e.g., WhatsApp, WeChat) will be applied in the intervention group. The chatting function of WhatsApp and WeChat will be used as the intervention platform. The intervention will start on the first day after the participants join the follow-up group. The whole interactive text-communication intervention lasts for 1 month. The frequency of message communication will be at least twice a week. After completing the intervention, participants will be invited to complete an individualized telephone-based interview for collecting further information on the intervention content.

Behavioral: Brief Motivational Interviewing interaction

control group

PLACEBO COMPARATOR

The participants in the control group will receive general health communication twice every week via SMS. The communication lasts for 1 month. After completing the intervention, participants will be invited to complete an individualized telephone-based interview for collecting further information on the intervention content.

Behavioral: General health communication

Interventions

Telephone peer counselling+ Brief Motivational Interviewing interaction, and telephone-based interview after receiving all information.

intervention group

Telephone peer counselling+ General health communication, and telephone-based interview, and telephone-based interview after receiving all information.

control group

Eligibility Criteria

Age13 Years - 25 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • age 25 years old or below,
  • report taking drugs within the past 30 days,
  • be able to speak Cantonese, read Traditional Chinese,
  • accept to received counseling use messaging apps (such as WhatsApp, WeChat, and SMS text messenger),
  • have verbally consented to join the follow-up intervention.

You may not qualify if:

  • have acute psychosis or other mental problems,
  • be undergoing other drug abuse recovery treatment.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

The University of Hong Kong

Hong Kong, Hong Kong

Location

Related Publications (3)

  • Saunders B, Wilkinson C, Phillips M. The impact of a brief motivational intervention with opiate users attending a methadone programme. Addiction. 1995 Mar;90(3):415-24. doi: 10.1046/j.1360-0443.1995.90341510.x.

  • Padwa H, Guerrero EG, Serret V, Rico M, Gelberg L. Adapting substance use brief interventions for adolescents: perspectives of adolescents living with adults in substance use disorder treatment. Subst Abuse Rehabil. 2018 Dec 5;9:137-142. doi: 10.2147/SAR.S177865. eCollection 2018.

  • de Gee EA, Verdurmen JE, Bransen E, de Jonge JM, Schippers GM. A randomized controlled trial of a brief motivational enhancement for non-treatment-seeking adolescent cannabis users. J Subst Abuse Treat. 2014 Sep;47(3):181-8. doi: 10.1016/j.jsat.2014.05.001. Epub 2014 May 17.

MeSH Terms

Conditions

Substance-Related DisordersAdolescent Behavior

Condition Hierarchy (Ancestors)

Chemically-Induced DisordersMental DisordersBehavior

Study Officials

  • Denise Shuk Ting Cheung, Phd

    HKU

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 9, 2020

First Posted

November 18, 2020

Study Start

November 15, 2020

Primary Completion

May 15, 2021

Study Completion

December 4, 2021

Last Updated

July 28, 2022

Record last verified: 2021-10

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 is completed and the results of the project have been published.
Access Criteria
Request could be sent to Principal Investigator (william3@hku.hk)

Locations