The Effectiveness Of Auricular Acupressure On Body Weight Parameters On Patients With Schizophrenia

Sponsor
TsaoTun Psychiatric Center, Department of Health, Taiwan (Other)
Overall Status
Unknown status
CT.gov ID
NCT01167348
Collaborator
(none)
86
1
2
42.9

Study Details

Study Description

Brief Summary

The purpose of this study is to examine whether auricular acupressure is effective in reducing body weight, waist circumference, or lipid profile.

Condition or Disease Intervention/Treatment Phase
  • Procedure: auricular acupressure
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
86 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
The Effectiveness Of Auricular Acupressure On Body Weight Parameters On Patients With Schizophrenia
Study Start Date :
Jun 1, 2010
Anticipated Primary Completion Date :
Aug 1, 2010
Anticipated Study Completion Date :
Aug 1, 2010

Outcome Measures

Primary Outcome Measures

  1. Using Body weight scale (kilogram) and checking body weight for all participants [2 months]

    all participants are going to be measured body weight per week for 2 months.

Secondary Outcome Measures

  1. waist circumference [2 months]

    All participants are going to be measured waist circumference per week for 2 months.

  2. Fat percentage by using bio-Impedance Analysis(Tanita-519 machine) [2 months]

    All participants will be measured fat percentage by BIA(Tanita-519) per 2 months.

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. ICD:295,living in chronic ward for more than 2 month

  2. Body Mass Index (BMI) >or=24

  3. Age between 20 to 60

  4. Psychotic status stable and can communicate

Exclusion Criteria:
  1. Unstable psychotic status

  2. Participants who have endocrine disease

  3. Participants who have cardiac disease

  4. Participants who have immunological disease

  5. Participants who have liver or renal function impairment

  6. Pregnant woman or in milking stage

  7. Cerebrovascular accident (CVA) stroke and disability

  8. Participant who attends weight control programs in recent 3 months

  9. Any conditions that clinical doctors refuse to let join in this study

Contacts and Locations

Locations

Site City State Country Postal Code
1 Tsao-Tun Psychiatric Center Nan-Tou Taiwan

Sponsors and Collaborators

  • TsaoTun Psychiatric Center, Department of Health, Taiwan

Investigators

  • Principal Investigator: Ching Han-Yi, MD, Tsaotun Psychiatric Center

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT01167348
Other Study ID Numbers:
  • Tsaotun Psychiatric Center
First Posted:
Jul 22, 2010
Last Update Posted:
Jul 23, 2010
Last Verified:
Jul 1, 2010
Keywords provided by , ,
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 23, 2010