- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00730600
Effect of THAI Traditional Massage on Bone Markers
August 6, 2008 updated by: Mahidol University
Acute Changes in Biochemical Markers of Bone Resorption and Formation After THAI Traditional Massage
The purpose of this study is to explore the skeletal effect of Thai traditional massage by examining the changes in biochemical markers of bone turnover immediately after the massage.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Each subject received Thai traditional massage for 2 hours by a single masseuse.
Study Type
Interventional
Enrollment (Actual)
30
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 Locations
-
-
-
Bangkok, Thailand, 10400
- Ramathibodi hospital
-
-
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
16 years to 36 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- Healthy Thai women aged 20 to 40 years
- Have been massaged by Thai Traditional massage style
Exclusion Criteria:
- Hyperparathyroidism, Thyrotoxicosis, Diabetes Mellitus, Rheumatoid Arthritis, Cancer
- Antiresorptive agent, Teriparatide and Glucocorticoid
- Swelling Joints
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
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: 1
1= THAI traditional massage
|
Thai traditional massage for 2 hours by a single masseuse.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Biochemical markers of bone resorption; C-terminal telopeptide of type I collagen (CTx-I) and of bone formation; total procollagen type 1 amino-terminal propeptide (P1NP)level
Time Frame: 2 hour
|
2 hour
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Sunee - Saetung, Msc, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand 10400
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, 2007
Primary Completion (Actual)
September 1, 2007
Study Completion (Actual)
July 1, 2008
Study Registration Dates
First Submitted
August 6, 2008
First Submitted That Met QC Criteria
August 6, 2008
First Posted (Estimate)
August 8, 2008
Study Record Updates
Last Update Posted (Estimate)
August 8, 2008
Last Update Submitted That Met QC Criteria
August 6, 2008
Last Verified
July 1, 2008
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ID 02-50-30
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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