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Clinical Trials/NCT03452241
NCT03452241CompletedNot Applicable

Long-term Follow-up Study of Substance Abuse Screening and Intervention in Multi Primary Care Centers

Shanghai Mental Health Center1 site in 1 country480 target enrollmentStarted: April 14, 2018Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
480
Locations
1
Primary Endpoint
Change from baseline in risk behaviors at 1 and 3 month

Study Overview

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 related medical staffs in five provinces 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 Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Screening
Masking
None

Eligibility Criteria

Ages
18 Years to 75 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •aged 18-75 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.

Arms & Interventions

Intervention Group

Experimental

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.

Intervention: Intervention Group (Other)

Control Group

Other

The participants only receive the materials about the harm of substance use

Intervention: Control Group (Other)

Intervention Group 1

Experimental

The medical staffs who received the training will use the manual of brief intervention twice to deliver it and other materials about the harm of substance use.

Intervention: Intervention Group (Other)

Outcomes

Primary Outcomes

Change from baseline in risk behaviors at 1 and 3 month

Time Frame: baseline, 1 and 3 month

Risk Behaviors will be measured by ASSIST questionnaire.

Secondary Outcomes

  • Knowledge related to Substance Use measured by Knowledge related to Addiction questionnaire(baseline, 1 and 3 month)
  • Depression measured by Self-Rating Depression Scale (SDS)(baseline, 1 and 3 month)
  • Self-esteem measured by Self-esteem questionnaire(baseline, 1 and 3 month)
  • Positive and Negative Affect measured by Positive and Negative Affect Scale (PANAS)(baseline, 1 and 3 month)
  • Motivation measured by Pre-treatment Readiness Scale(baseline, 1 and 3 month)
  • Anxiety measured by Self-Rating Anxiety Scale (SAS).(baseline, 1 and 3 month)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

DU, Jiang

Principal Investigator

Shanghai Mental Health Center

Study Sites (1)

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