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Peer-delivered Brief Motivational Interviewing Via Instant Messaging Interaction in Reducing the Drug Abuse Among Youth

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ClinicalTrials.gov Identifier: NCT04672746
Recruitment Status : Not yet recruiting
First Posted : December 17, 2020
Last Update Posted : December 21, 2020
Sponsor:
Information provided by (Responsible Party):
The University of Hong Kong

Brief Summary:
This is a two-arm, parallel-group, randomized controlled trial with an allocation ratio 1:1, by comparing the 12-month drug abuse reduction between the youth drug abusers who are individually randomized to participate in the intervention group receiving medical peer-delivered intervention of interactive brief motivational interviewing via instant messaging communication and those in the control group receiving general health information.

Condition or disease Intervention/treatment Phase
Drug Abuse Adolescent Behavior Behavioral: Brief MI interaction via instant communication Behavioral: General health information Not Applicable

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 134 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Treatment
Official Title: The Medical Peer-delivered Intervention of Brief Motivational Interviewing Via Instant Messaging Interaction in Reducing the Drug Abuse Among Youth in Hong Kong: A Randomized Controlled Trial
Estimated Study Start Date : March 2021
Estimated Primary Completion Date : August 2022
Estimated Study Completion Date : December 2023

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: Brief MI interaction via instant communication
The interaction communication using brief motivational interviewing will be applied via the chatting function of instant messaging apps (e.g., WhatsApp, WeChat). The intervention will last for 6 month with a frequency of at least twice a week.
Behavioral: Brief MI interaction via instant communication
Telephone peer counselling+referral to treatment if required+The interaction communication using brief motivational interviewing via the chatting function of instant messaging apps (e.g., WhatsApp, WeChat). The intervention will last for 6 month with a frequency of at least twice a week.

Placebo Comparator: General health information
The subjects will receive general health information via SMS, such as "do physical exercise for at least 30 min per week will keep you healthy" for 6 month with a frequency of least twice a week.
Behavioral: General health information
Telephone peer counselling+referral to treatment if required+general health information via SMS, such as "do physical exercise for at least 30 min per week will keep you healthy" for 6 month with a frequency of least twice a week.




Primary Outcome Measures :
  1. Changes in drug consumption at 12 months comparing to that at baseline [ Time Frame: 12 month ]
    The participants' changes in drug consumption between baseline and 12 months follow-up measured using a structured-questionnaire gathering the frequency and categoties 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.


Secondary Outcome Measures :
  1. Changes in drug consumption at 6 month comparing to that at baseline [ Time Frame: 6 month ]
    The participants' changes in drug consumption between baseline and 6 months follow-up using using a structured-questionnaire gathering the frequency and categoties 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.

  2. 30 days self-reported drug abstinence at 6 months [ Time Frame: 6 month ]
    The participants' 30 days self-reported drug abstinence at 6 months follow-up measured using using a structured-questionnaire gathering the frequency and categoties of drug consumption in the past 30 days. The self-reported non-drug consumption indicating drug abstinence.

  3. 30 days self-reported drug abstinence at 12 months [ Time Frame: 12 month ]
    The participants' 30 days self-reported drug abstinence at 12 months follow-up measured using using a structured-questionnaire gathering the frequency and categoties of drug consumption in the past 30 days. The self-reported non-drug consumption indicating drug abstinence.

  4. Changes in relapse risk among the quitters at 6 months comparing to that at baseline [ Time Frame: 6 month ]
    The participants' changes in relapse risk between baseline and 6 months follow-up measured using the Stimulant Relapse Risk Scale (Chinese version). The scale consists of 27 items and measures the risk of stimulant reuse in 5 dimensions: anxiety and intention to use drug, emotionality problems, compulsivity for drug use, positive expectancies and lack of control over drug, and lack of negative expectancy for drug use.

  5. Changes in relapse risk among the quitters at 12 months comparing to that at baseline [ Time Frame: 12 month ]
    The participants' changes in relapse risk between baseline and 12 months follow-up measured using the Stimulant Relapse Risk Scale (Chinese version). The scale consists of 27 items and measures the risk of stimulant reuse in 5 dimensions: anxiety and intention to use drug, emotionality problems, compulsivity for drug use, positive expectancies and lack of control over drug, and lack of negative expectancy for drug use.

  6. Changes in the contemplation stages at 6 months comparing to that at baseline [ Time Frame: 6 month ]
    The participants' changes in the contemplation stages between baseline,and 6 months follow-up measured using the Contemplation Ladder Tool. The tool consists of 5 items which include pre-contemplation stage, contemplation stage, decision stage, action stage, and maintenance stage.

  7. Changes in the contemplation stages at 12 months comparing to that at baseline [ Time Frame: 12 month ]
    The participants' changes in the contemplation stages between baseline, and 12 months follow-up measured using the Contemplation Ladder Tool. The tool consists of 5 items which include pre-contemplation stage, contemplation stage, decision stage, action stage, and maintenance stage.

  8. Changes of motivation towards solving the problem at 6 months comparing to that at baseline [ Time Frame: 6 month ]
    Participants' changes of motivation towards solving the problem between baseline and 6 months follow up measured using the Chinese version of Treatment Needs/Motivation Scales (TCU MOTForm). The scale consists of 36 items with 5 dimensions: Problem Recognition (PR), Desire for Help (DH), Treatment Readiness (TR), Pressures for Treatment (PT), and Treatment Needs (TN), which are using a 5-likert score. The score of the scale ranges from 36 to 180, with higher score indicating a higher motivation towards solving the problem.

  9. Changes of motivation towards solving the problem at 12 months comparing to that at baseline [ Time Frame: 12 month ]
    Participants' changes of motivation towards solving the problem between baseline and 12 months follow up measured using the Chinese version of Treatment Needs/Motivation Scales (TCU MOTForm). The scale consists of 36 items with 5 dimensions: Problem Recognition (PR), Desire for Help (DH), Treatment Readiness (TR), Pressures for Treatment (PT), and Treatment Needs (TN), which are using a 5-likert score. The score of the scale ranges from 36 to 180, with higher score indicating a higher motivation towards solving the problem.



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Ages Eligible for Study:   up to 25 Years   (Child, Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • aged ≤ 25 years;
  • report taking drugs within the past 30 days;
  • be able to speak Cantonese and 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

Exclusion Criteria:

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

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04672746


Contacts
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Contact: William Ho cheung Li, PhD 39176634 william3@hku.hk

Locations
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Hong Kong
The University of Hong Kong
Hong Kong, Hong Kong
Sponsors and Collaborators
The University of Hong Kong
Investigators
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Study Director: William Li, PhD The University of Hong Kong
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Responsible Party: The University of Hong Kong
ClinicalTrials.gov Identifier: NCT04672746    
Other Study ID Numbers: MedPAC-RCT
First Posted: December 17, 2020    Key Record Dates
Last Update Posted: December 21, 2020
Last Verified: December 2020
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Yes
Plan Description: 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)

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by The University of Hong Kong:
drug abuse
brief motivational interview
peer counselling
instant messaging
adolescent
Additional relevant MeSH terms:
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Substance-Related Disorders
Chemically-Induced Disorders
Mental Disorders