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Health Promotion on Young Adults With High Risk Disability for Mental Health (HPMI)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT01740167
Recruitment Status : Unknown
Verified November 2012 by China Medical University Hospital.
Recruitment status was:  Active, not recruiting
First Posted : December 4, 2012
Last Update Posted : December 4, 2012
Sponsor:
Collaborator:
National Science Council, Taiwan
Information provided by (Responsible Party):
China Medical University Hospital

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.

Condition or disease Intervention/treatment Phase
Mental Health Wellness 1 Behavioral: health promotion lifestyle program Not Applicable

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.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 200 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Masking: Single (Participant)
Primary Purpose: Prevention
Official Title: Health Promotion on Young Adults With High Risk Disability for Mental Health: Development and Evaluation of the Screen Prevention Model
Study Start Date : November 2012
Estimated Primary Completion Date : October 2013
Estimated Study Completion Date : October 2015

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Mental Health

Arm Intervention/treatment
Experimental: Lifestyle program
health promotion lifestyle program : individual counseling, once a month, total 3 times.
Behavioral: health promotion lifestyle program
Individual counseling, once a month, total 3 times.




Primary Outcome Measures :
  1. Chinese version of Health-Promotion Lifestyle Profile-Short [ Time Frame: 3 months ]

Secondary Outcome Measures :
  1. Chinese version of Schizotypal Personality Questionnaire-Brief [ Time Frame: 3 months ]

Other Outcome Measures:
  1. Chinese mandarin version of State-Trait Anxiety Inventory from Y [ Time Frame: 3 months ]
  2. simple physical assessment [ Time Frame: 3 months ]
  3. Personal Inventory [ Time Frame: 3 months ]
  4. 3 months physical activity assessment [ Time Frame: 3 months ]


Information from the National Library of Medicine

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Ages Eligible for Study:   20 Years to 65 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

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.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01740167


Locations
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Taiwan
China Medical University
Taichung, Taiwan, 40402
Sponsors and Collaborators
China Medical University Hospital
National Science Council, Taiwan
Investigators
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Principal Investigator: Wei-Fen Ma, PHD China Medical University, Taiwan
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Responsible Party: China Medical University Hospital
ClinicalTrials.gov Identifier: NCT01740167    
Other Study ID Numbers: NSC101-2511-S-039-003
DMR101-IRB2-222 ( Other Identifier: ChinaMUH )
First Posted: December 4, 2012    Key Record Dates
Last Update Posted: December 4, 2012
Last Verified: November 2012
Keywords provided by China Medical University Hospital:
prodrome
mental illness
health promotion
lifestyle behavior