- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02951858
Substance Use Screening Among Drug User
October 31, 2016 updated by: DU, Jiang, Shanghai Mental Health Center
Screening and Brief Interventions for Substance Use in Primary Medical Institution
The purpose of this research is to improve the ability of primary medical staffs in screening and intervention for alcohol, benzodiazepines, and other illicit drug use.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
In order to reduce the social and personal harm caused by drugs, it is urgent to strengthen the ability of the primary health institutions in screening and intervention the addictive substances use.
Firstly, the investigators will invite 10 primary medical staffs and 10 experts in addition to revise the manual of Alcohol, Smoking, and Substance Use Involvement Screening Test (ASSIST) and Brief Intervention (BI).
Then, the investigators will recruit 100 medical staffs to participate the training of ASSIST and BI.
Secondly, the researcher will investigate the effects of BI technology in reducing the use of addictive substances, improve the addiction related knowledge of patients through randomized controlled study.
Finally, the investigators will collect the research information, revise the manual, and promote the training.
Study Type
Interventional
Enrollment (Anticipated)
218
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 60 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- aged 18-60 years;
- the patient to the community medical institutions;
- ASSIST score is in 12-27, in a moderate risk;
- voluntary to participate;
- to agree to complete baseline interviews and follow-up studies.
Exclusion Criteria:
- unable to complete the questionnaire;
- serious physical illness, action inconvenience.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Intervention Group
The medical staffs who received the training will use the manual of brief intervention to deliver it and other materials about the harm of substance use.
|
The medical staffs who received the training will use the manual of brief intervention to deliver BI and other materials about the harm of substance use.
|
Active Comparator: Control Group
The participants only receive the materials about the harm of substance use.
|
The participants only receive the materials about the harm of substance use.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Risk Behaviors measured by ASSIST questionnaire
Time Frame: 1 month
|
Risk Behaviors will be measured by ASSIST questionnaire.
|
1 month
|
Knowledge related to Substance Use measured by Knowledge related to Addiction questionnaire
Time Frame: 1 month
|
Knowledge related to substance use will be measured by Knowledge related to Addiction questionnaire.
|
1 month
|
Motivation measured by Pre-treatment Readiness Scale
Time Frame: 1 month
|
Motivation will be measured by Pre-treatment Readiness Scale (PRS).
|
1 month
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Depression measured by Self-Rating Depression Scale
Time Frame: 1 month
|
the change of depression will be measured by Self-Rating Depression Scale (SDS).
|
1 month
|
Anxiety measured by Self-Rating Anxiety Scale
Time Frame: 1 month
|
the change of anxiety will be measured by Self-Rating Anxiety Scale (SAS).
|
1 month
|
Self-esteem measured by Self-esteem questionnaire
Time Frame: 1 month
|
the change of self-esteem will be measured by Self-esteem questionnaire.
|
1 month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Jiang Du, M.D, Shanghai Mental Health Center
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2017
Primary Completion (Anticipated)
December 1, 2018
Study Registration Dates
First Submitted
October 23, 2016
First Submitted That Met QC Criteria
October 31, 2016
First Posted (Estimate)
November 1, 2016
Study Record Updates
Last Update Posted (Estimate)
November 1, 2016
Last Update Submitted That Met QC Criteria
October 31, 2016
Last Verified
October 1, 2016
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- JDu-003
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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