- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01422447
Research of Prevention and Intervention of Mental Health Problems (RPIMHP)
November 24, 2015 updated by: Shanghai Mental Health Center
Prevention and Mental Health Education for Mental Health Problems in Community: A Model of Common Mental Health Problems in Seven Metropolis of China
The purpose of this research is to establish a suitable community-based model for Chinese culture,to improve the community recognition of common mental disorders,as well as its treatment and control.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The project will select seven metropolis,through multi-center collaborative research,use of interdisciplinary methods and combining qualitative and quantitative research methods.Community resources will be integrated so as to build the Chinese model of community mental health services and to establish the routine for common mental disorders.
Evaluation criteria for community mental health needs to be developed for the process of health education and intervention techniques.
Study Type
Interventional
Enrollment (Actual)
42016
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.
Study Locations
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Beijing
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Beijing, Beijing, China
- Capital Normal University
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Guangdong
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Shenzhen, Guangdong, China
- Shenzhen mental health center
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Hunan
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Hunan, Hunan, China
- Mental Health Center in Hunan Province
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Jilin
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Harbin, Jilin, China
- Harbin Medical University
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Shanghai
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Shanghai, Shanghai, China, 200030
- 中国
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Sichuan
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Sichuan, Sichuan, China
- Mental Health of Sichuan Province
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Xinjiang
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Xinjiang, Xinjiang, China
- Mental Health of Xinjiang Province
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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
13 years to 65 years (Child, Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- general population: 13-65-year-old,
- high-risk groups: not yet shown symptoms of mental disorders, but exposed to epidemiological risk factors for anxiety,depression and alcohol abuse.A part may be at risk for future depression,anxiety and alcohol abuse,for example: post-disaster population,Stress-related groups, the unemployed and laid-off people, high risk of psychological disorders (chronic treatment of various medical institutions and disabled, the mentally ill family members).
- early stage of mental disorders in population:the subjects have the problem of depression, anxiety or alcohol abuse, but not yet diagnosed with depression, anxiety disorders or alcohol abuse.
Exclusion Criteria:
those who have been diagnosed with depression,anxiety or alcohol abuse and other psychiatric disorders will be excluded from this study.
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: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: community intervention
Feedback on assessment results: distribute relevant brochures and hold regular lectures on depression, anxiety and alcohol-abuse.
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in addition to regular intervention, those subjects in the intervention group will be given education intervention.
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Active Comparator: regular intervention control
the subjects in the control group live in the used model
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the subjects in the control group live in the used model
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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evaluate the changes of mental health state of community residents before and after intervention
Time Frame: 12 months
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we will use several scales such as SRHMS,SE,SEI,PSS,SCSQ,PHQ,AUDIT,scale of mental health knowledge and attitude survey and suicide related problems to evaluate the effect of our intervention.
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12 months
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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prevalence of depression,anxiety and alcohol abuse
Time Frame: 12 months
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use scales of PHQ-9,PHQ-7 and AUDIT to investigate prevalence of depression,anxiety and alcohol abuse.
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12 months
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public awareness and attitude towards mental health knowledge
Time Frame: 12 months
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designed related questionnaires to investigate the public's awareness and attitude towards mental health knowledge.
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12 months
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service needs and utilization
Time Frame: 12 months
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use qualitative research methods to ivestigate service needs and utilization of three target population in community.
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12 months
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the reliability and validity of PHQ-9, HPQ-7 and AUDIT
Time Frame: 6 months
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use MINI as the gold standard to evaluate the reliability and validity of PHQ-9, HPQ-7 and AUDIT in community and university students
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6 months
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assessment of the situation of community mental health service resources
Time Frame: 1 month
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we use scales to evaluate the situation of community mental health service resources
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1 month
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assessment the changes of early stage of mental disorders in population before and after intervention
Time Frame: 3 months
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we will use several sacles such as assessment scale of motivation changes,alclhol behavior and willingness and confidence of abstain from drinking to evaluate the changes before and after intervention with people who have alcohol abuse problems and use SAS,SDS and IBS to evaluate the changes in people who have depression and anxiety problems.
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3 months
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Min ZHAO,, Ph.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
October 1, 2010
Primary Completion (Actual)
December 1, 2012
Study Completion (Actual)
December 1, 2012
Study Registration Dates
First Submitted
August 18, 2011
First Submitted That Met QC Criteria
August 22, 2011
First Posted (Estimate)
August 24, 2011
Study Record Updates
Last Update Posted (Estimate)
November 25, 2015
Last Update Submitted That Met QC Criteria
November 24, 2015
Last Verified
November 1, 2015
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- MZhao-001
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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