Viewing Study NCT01740167


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Study NCT ID: NCT01740167
Status: UNKNOWN
Last Update Posted: 2012-12-04
First Post: 2012-11-28
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Health Promotion on Young Adults With High Risk Disability for Mental Health
Sponsor: China Medical University Hospital
Organization:

Study Overview

Official Title: Health Promotion on Young Adults With High Risk Disability for Mental Health: Development and Evaluation of the Screen Prevention Model
Status: UNKNOWN
Status Verified Date: 2012-11
Last Known Status: ACTIVE_NOT_RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: HPMI
Brief Summary: 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: 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.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?:

Secondary ID Infos

Secondary ID Type Domain Link View
DMR101-IRB2-222 OTHER ChinaMUH View