- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02067312
Effects of Traditional Thai Massage on Pain and Pain Related Parameters in Patients With Upper Back Pain
May 5, 2015 updated by: Dr. Vitsarut Buttagat, Mae Fah Luang University Hospital
The purpose of this study is to determine the effect of Thai massage on pain related parameters including Pain intensity, 24 hours pain intensity, Pressure pain threshold, anxiety, muscle tension, cervical range of motion, pain frequency, patient satisfaction and side effect in patients with chronic upper back pain associated with myofascial trigger points
Study Overview
Study Type
Interventional
Enrollment (Actual)
50
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
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Chiang Rai
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Mueang, Chiang Rai, Thailand, 57100
- School of Health Science, Mae Fah Luang University
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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
18 years to 40 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 upper pain for longer than 12 weeks (chronic) and that at least one trigger point will be present in the s 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:
- Cervical radiculopathy
- 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: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Thai massage
The participants will receive a thirty minutes session of Thai massage onto the trapezius muscle
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Sham Comparator: Sham Microwave diathermy
The participants will receive a thirty minutes session of Sham microwave diathermy onto the trapezius muscle
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Pain score on Visual analog scale
Time Frame: 5 weeks
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The intensity of pain will be reported by the participant on a visual analog scale ranging from 0 to 10. Zero indicates no pain anywhere and 10 indicates the most pain ever experienced.
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5 weeks
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Pressure Pain Threshold as a measure by algometry
Time Frame: 5 weeks
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5 weeks
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Muscle tension on Visual analog scale
Time Frame: 5 weeks
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5 weeks
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Anxiety on State Anxiety Inventory
Time Frame: 5 weeks
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5 weeks
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Cervical range of motion as a measure by Cervical Range of Motion Goniometer
Time Frame: 5 weeks
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5 weeks
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Pain intensity on McGill Pain Questionnaire
Time Frame: 5 weeks
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5 weeks
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Pain frequency occurred per week
Time Frame: 5 weeks
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5 weeks
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24 hours pain intensity on Visual analog scale
Time Frame: 5 weeks
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5 weeks
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Patient satisfaction level
Time Frame: 3 weeks
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3 weeks
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Number of Participants with Adverse Events
Time Frame: 3 weeks
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3 weeks
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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
February 1, 2014
Primary Completion (Actual)
June 1, 2014
Study Completion (Actual)
June 1, 2014
Study Registration Dates
First Submitted
February 17, 2014
First Submitted That Met QC Criteria
February 18, 2014
First Posted (Estimate)
February 20, 2014
Study Record Updates
Last Update Posted (Estimate)
May 6, 2015
Last Update Submitted That Met QC Criteria
May 5, 2015
Last Verified
May 1, 2015
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 55218152
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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