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Status unknownNCT01740167HPMIUpdated Dec 4, 2012

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

An interventional study of health promotion lifestyle program in Mental Health Wellness 1, sponsored by China Medical University Hospital. Status unknown at 1 site in Taiwan. Open to participants aged 20 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2012-12-04.

Sponsored by China Medical University Hospital · Not applicable, Interventional, and Prevention

The sponsor has not verified this record recently (last verified Nov 2012), so the status shown — last known as Active, not recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
200
Allocation
Not applicable
Ages
20 Years to 65 Years
Sex
All
01

Study 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.
Read the 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.

02

Conditions studied

  • Mental Health Wellness 1

Keywords

  • prodrome
  • mental illness
  • health promotion
  • lifestyle behavior
03

In context

Lead sponsor

China Medical University Hospital is the lead sponsor of 464 studies on the registry; 116 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

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

Exclusion Criteria:

  • had been diagnosed as schizophrenia, bipolar disorders, and major depression.
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Not applicable
Intervention model
Single group
Masking
Single (Participant)
Enrollment
200 participants (estimated)

Study arms

  • Experimental
    Lifestyle program

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

    Behavioral: health promotion lifestyle program

Interventions

  • Behavioralhealth promotion lifestyle program

    Individual counseling, once a month, total 3 times.

06

What researchers measure

Primary outcomes

  1. Chinese version of Health-Promotion Lifestyle Profile-Short

    Time frame: 3 months

Secondary outcomes

  1. Chinese version of Schizotypal Personality Questionnaire-Brief

    Time frame: 3 months

Other outcomes

  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

07

Study locations

1 site
  • China Medical University
    Taichung, 40402, Taiwan
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 4, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01740167
Lead sponsor
China Medical University Hospital
Collaborators
National Science Council, Taiwan
Responsible party
Sponsor
First posted
Dec 4, 2012
Start date
Nov 2012
Primary completion
Oct 2013 (estimated)
Completion
Oct 2015 (estimated)
Last update
Dec 4, 2012

Study contacts

Wei-Fen Ma, PHD
principal investigator · China Medical University, Taiwan

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Nov 2012. You cannot join it, but the record below documents what was studied.

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