NCT01740167

Brief Summary

  1. 1.The positive outcomes reported by participants in experimental group after two weeks of interventions will be significantly better than before interventions.
  2. 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. 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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
200

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Nov 2012

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 1, 2012

Completed
27 days until next milestone

First Submitted

Initial submission to the registry

November 28, 2012

Completed
6 days until next milestone

First Posted

Study publicly available on registry

December 4, 2012

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2013

Completed
2 years until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2015

Completed
Last Updated

December 4, 2012

Status Verified

November 1, 2012

Enrollment Period

11 months

First QC Date

November 28, 2012

Last Update Submit

November 30, 2012

Conditions

Mental Health Wellness 1

Keywords

prodromemental illnesshealth promotionlifestyle behavior

Outcome Measures

Primary Outcomes (1)

  • Chinese version of Health-Promotion Lifestyle Profile-Short

    3 months

Secondary Outcomes (1)

  • Chinese version of Schizotypal Personality Questionnaire-Brief

    3 months

Other Outcomes (4)

  • Chinese mandarin version of State-Trait Anxiety Inventory from Y

    3 months

  • simple physical assessment

    3 months

  • Personal Inventory

    3 months

  • +1 more other outcomes

Study Arms (1)

Lifestyle program

EXPERIMENTAL

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

Behavioral: health promotion lifestyle program

Interventions

health promotion lifestyle programBEHAVIORAL

Individual counseling, once a month, total 3 times.

Lifestyle program

Eligibility Criteria

Age20 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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.

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

China Medical University

Taichung, 40402, Taiwan

Location

MeSH Terms

Conditions

Mental Disorders

Study Officials

  • Wei-Fen Ma, PHD

    China Medical University, Taiwan

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
PREVENTION
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 28, 2012

First Posted

December 4, 2012

Study Start

November 1, 2012

Primary Completion

October 1, 2013

Study Completion

October 1, 2015

Last Updated

December 4, 2012

Record last verified: 2012-11

Locations

TW(1)