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

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

Study Overview

Status

Unknown

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Anticipated)

86

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

20 years to 60 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Using Body weight scale (kilogram) and checking body weight for all participants
Time Frame: 2 months
all participants are going to be measured body weight per week for 2 months.
2 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
waist circumference
Time Frame: 2 months
All participants are going to be measured waist circumference per week for 2 months.
2 months
Fat percentage by using bio-Impedance Analysis(Tanita-519 machine)
Time Frame: 2 months
All participants will be measured fat percentage by BIA(Tanita-519) per 2 months.
2 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

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

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

June 1, 2010

Primary Completion (Anticipated)

August 1, 2010

Study Completion (Anticipated)

August 1, 2010

Study Registration Dates

First Submitted

July 16, 2010

First Submitted That Met QC Criteria

July 21, 2010

First Posted (Estimate)

July 22, 2010

Study Record Updates

Last Update Posted (Estimate)

July 23, 2010

Last Update Submitted That Met QC Criteria

July 22, 2010

Last Verified

July 1, 2010

More Information

Terms related to this study

Other Study ID Numbers

  • Tsaotun Psychiatric Center

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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