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Health Promotion on Young Adults With High Risk Disability for Mental Health

NCT ID: NCT01740167

Last Updated: 2012-12-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

200 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-11-30

Study Completion Date

2015-10-31

Brief Summary

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1. The positive outcomes reported by participants in experimental group after two weeks of interventions will be significantly better than before interventions.
2. The positive outcomes reported by participants in experimental group will be significantly better than those in control group after two weeks of providing prevention model interventions.
3. The positive outcomes reported by participants in experimental group will be significantly better than those in control group after six months of providing prevention model interventions.

Detailed Description

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Early finding for people with high mental risk plays the important role in mental health promotion. In literature, before specific psychotic symptoms appear, individuals may experience a period of nonspecific symptoms and growing functional impairment. Early interventions may alter the natural course of mental diseases and improve treatment outcomes. So that, the purpose of this study is to develop a screen and prevention mode for identifying young adults with high risk status of mental health disability. The psychosocial intervention strategies for emotional and cognitive support in prevention model based on health promotion theory will be used for this study. Participants in this experimental design study will be randomly assigned into experimental and control groups. Four scales and objective physical assessments are used for evaluating study outcomes. The pre- and post-test will be held before and one week after prevention interventions. In addition, follow-ups will be included for understanding long-term outcomes of the effectiveness of the screen prevention model.

Conditions

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Mental Health Wellness 1

Keywords

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prodrome mental illness health promotion lifestyle behavior

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Participants

Study Groups

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Lifestyle program

health promotion lifestyle program : individual counseling, once a month, total 3 times.

Group Type EXPERIMENTAL

health promotion lifestyle program

Intervention Type BEHAVIORAL

Individual counseling, once a month, total 3 times.

Interventions

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health promotion lifestyle program

Individual counseling, once a month, total 3 times.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* age 20-65 years, (Chinese version of Schizotypal Personality Questionnaire-Brief \> 17 scores, or Chinese Mandarin State Trait Anxiety Inventory Y2 \> 60 scores), and agree to participants.

Exclusion Criteria

* had been diagnosed as schizophrenia, bipolar disorders, and major depression.
Minimum Eligible Age

20 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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National Science and Technology Council, Taiwan

OTHER_GOV

Sponsor Role collaborator

China Medical University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Wei-Fen Ma, PHD

Role: PRINCIPAL_INVESTIGATOR

China Medical University, Taiwan

Locations

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China Medical University

Taichung, , Taiwan

Site Status

Countries

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Taiwan

Other Identifiers

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DMR101-IRB2-222

Identifier Type: OTHER

Identifier Source: secondary_id

NSC101-2511-S-039-003

Identifier Type: -

Identifier Source: org_study_id