- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01168180
Traditional Thai Massage and Scapulocostal Syndrome
August 13, 2012 updated by: Khon Kaen University
Efficacy of Traditional Thai Massage on Patients With Scapulocostal Syndrome
The purpose of this study is to evaluate the efficacy of traditional Thai massage on pain intensity, pressure pain threshold, muscle tension, anxiety, cervical range of motion, patient satisfaction and side effects in the treatment of scapulocostal syndrome.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
60
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
-
-
Khon Kaen
-
Muang, Khon Kaen, Thailand, 40002
- Faculty of Associated Medical Sciences, Khon Kaen University
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Muang, Khon Kaen, Thailand, 40002
- School of physical therapy, Faculty of Associated medical sciences, Khon Kaen University
-
-
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
14 years to 46 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Male or female
- Age between 18 - 50 years old
- The participants have experienced spontaneous scapular pain (VAS ≥ 3) for longer than 12 weeks (chronic) and that at least one trigger point will be present in the scapular region (serratus posterior superior, rhomboid groups, levator scapulae and trapezius muscles). Trigger points will be diagnosed as the presence of focal tenderness in a taut band and with pain recognition.
- The participants will be able to follow instructions.
- Good communication and cooperation.
Exclusion Criteria:
A history of the following diseases or disorders:
- Rotator cuff disease
- Cervical radiculopathy
- Degenerative shoulder joint disease
- Shoulder stiffness
Contraindications of traditional Thai massage
- Contagious skin disease
- Injury or inflammation of muscle
- Bone fracture and/or joint dislocation
- Open wound
- Uncontrolled hypertension
- Drug and/or alcohol intoxication
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
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Traditional Thai massage
The participants will receive thirty minutes session of traditional Thai massage onto the scapular region for 9 sessions over a period of 3 weeks
|
The participants will receive thirty minutes session of traditional Thai massage onto the scapular region for 9 sessions over a period of 3 weeks
|
|
Active Comparator: Ultrasound therapy and hot pack
The participants will receive thirty minutes session of Ultrasound therapy and hot pack for 9 sessions over a period of 3 weeks
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain intensity (Visual analog scale)
Time Frame: 4 months
|
The intensity of pain will be reported by the participant on a numerical analog scale ranging from 0 to 10. Zero indicates no pain anywhere and 10 indicates the most pain ever experienced.
|
4 months
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Pressure Pain Threshold
Time Frame: 4 months
|
4 months
|
|
Muscle tension (Visual analog scale)
Time Frame: 4 months
|
4 months
|
|
State Anxiety Inventory
Time Frame: 4 months
|
4 months
|
|
patient satisfaction
Time Frame: 3 weeks
|
3 weeks
|
|
Side effects
Time Frame: 3 weeks
|
3 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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
July 1, 2010
Primary Completion (Actual)
December 1, 2011
Study Completion (Actual)
December 1, 2011
Study Registration Dates
First Submitted
July 19, 2010
First Submitted That Met QC Criteria
July 22, 2010
First Posted (Estimate)
July 23, 2010
Study Record Updates
Last Update Posted (Estimate)
August 14, 2012
Last Update Submitted That Met QC Criteria
August 13, 2012
Last Verified
June 1, 2011
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 527090004-4
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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