Substance Use Screening Among Drug User
Primary Purpose
Substance Use
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Intervention Group
Control Group
Sponsored by
About this trial
This is an interventional treatment trial for Substance Use focused on measuring Alcohol,Smoking,and Substance Use Involvement Screening Test, Brief Intervention, Substance Use, Primary Medical and Health Care Institution
Eligibility Criteria
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.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Intervention Group
Control Group
Arm Description
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 participants only receive the materials about the harm of substance use.
Outcomes
Primary Outcome Measures
Risk Behaviors measured by ASSIST questionnaire
Risk Behaviors will be measured by ASSIST questionnaire.
Knowledge related to Substance Use measured by Knowledge related to Addiction questionnaire
Knowledge related to substance use will be measured by Knowledge related to Addiction questionnaire.
Motivation measured by Pre-treatment Readiness Scale
Motivation will be measured by Pre-treatment Readiness Scale (PRS).
Secondary Outcome Measures
Depression measured by Self-Rating Depression Scale
the change of depression will be measured by Self-Rating Depression Scale (SDS).
Anxiety measured by Self-Rating Anxiety Scale
the change of anxiety will be measured by Self-Rating Anxiety Scale (SAS).
Self-esteem measured by Self-esteem questionnaire
the change of self-esteem will be measured by Self-esteem questionnaire.
Full Information
NCT ID
NCT02951858
First Posted
October 23, 2016
Last Updated
October 31, 2016
Sponsor
Shanghai Mental Health Center
1. Study Identification
Unique Protocol Identification Number
NCT02951858
Brief Title
Substance Use Screening Among Drug User
Official Title
Screening and Brief Interventions for Substance Use in Primary Medical Institution
Study Type
Interventional
2. Study Status
Record Verification Date
October 2016
Overall Recruitment Status
Unknown status
Study Start Date
January 2017 (undefined)
Primary Completion Date
December 2018 (Anticipated)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Shanghai Mental Health Center
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
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.
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Substance Use
Keywords
Alcohol,Smoking,and Substance Use Involvement Screening Test, Brief Intervention, Substance Use, Primary Medical and Health Care Institution
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
218 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Intervention Group
Arm Type
Experimental
Arm Description
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.
Arm Title
Control Group
Arm Type
Active Comparator
Arm Description
The participants only receive the materials about the harm of substance use.
Intervention Type
Behavioral
Intervention Name(s)
Intervention Group
Intervention Description
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.
Intervention Type
Behavioral
Intervention Name(s)
Control Group
Intervention Description
The participants only receive the materials about the harm of substance use.
Primary Outcome Measure Information:
Title
Risk Behaviors measured by ASSIST questionnaire
Description
Risk Behaviors will be measured by ASSIST questionnaire.
Time Frame
1 month
Title
Knowledge related to Substance Use measured by Knowledge related to Addiction questionnaire
Description
Knowledge related to substance use will be measured by Knowledge related to Addiction questionnaire.
Time Frame
1 month
Title
Motivation measured by Pre-treatment Readiness Scale
Description
Motivation will be measured by Pre-treatment Readiness Scale (PRS).
Time Frame
1 month
Secondary Outcome Measure Information:
Title
Depression measured by Self-Rating Depression Scale
Description
the change of depression will be measured by Self-Rating Depression Scale (SDS).
Time Frame
1 month
Title
Anxiety measured by Self-Rating Anxiety Scale
Description
the change of anxiety will be measured by Self-Rating Anxiety Scale (SAS).
Time Frame
1 month
Title
Self-esteem measured by Self-esteem questionnaire
Description
the change of self-esteem will be measured by Self-esteem questionnaire.
Time Frame
1 month
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jiang Du, M.D
Phone
18017311220
Email
dujiangdou@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jiang Du, M.D
Organizational Affiliation
Shanghai Mental Health Center
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
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Substance Use Screening Among Drug User
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