Peer-delivered Brief Motivational Interviewing Via Instant Messaging Interaction in Reducing the Drug Abuse Among Youth
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| ClinicalTrials.gov Identifier: NCT04672746 |
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Recruitment Status :
Not yet recruiting
First Posted : December 17, 2020
Last Update Posted : December 21, 2020
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Drug Abuse Adolescent Behavior | Behavioral: Brief MI interaction via instant communication Behavioral: General health information | Not Applicable |
Show detailed description
| 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 |
| Arm | Intervention/treatment |
|---|---|
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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.
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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. |
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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.
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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. |
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | up to 25 Years (Child, Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
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.
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
| Contact: William Ho cheung Li, PhD | 39176634 | william3@hku.hk |
| Hong Kong | |
| The University of Hong Kong | |
| Hong Kong, Hong Kong | |
| Study Director: | William Li, PhD | The University of Hong Kong |
| 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) |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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drug abuse brief motivational interview peer counselling instant messaging adolescent |
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Substance-Related Disorders Chemically-Induced Disorders Mental Disorders |

