- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01167348
The Effectiveness Of Auricular Acupressure On Body Weight Parameters On Patients With Schizophrenia
July 22, 2010 updated by: TsaoTun Psychiatric Center, Department of Health, Taiwan
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
- Name: Han-Yi Ching, MD
- Phone Number: 886911587276
- Email: HYChing@mail.ttpc.doh.gov.tw
Study Locations
-
-
-
Nan-Tou, Taiwan
- Recruiting
- Tsao-Tun Psychiatric Center
-
Contact:
- Han-Yi Ching, MD
- Phone Number: 886911587276
- Email: HYChing@mail.ttpc.doh.gov.tw
-
-
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:
- ICD:295,living in chronic ward for more than 2 month
- Body Mass Index (BMI) >or=24
- Age between 20 to 60
- Psychotic status stable and can communicate
Exclusion Criteria:
- Unstable psychotic status
- Participants who have endocrine disease
- Participants who have cardiac disease
- Participants who have immunological disease
- Participants who have liver or renal function impairment
- Pregnant woman or in milking stage
- Cerebrovascular accident (CVA) stroke and disability
- Participant who attends weight control programs in recent 3 months
- 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
Additional Relevant MeSH Terms
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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