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

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
      • 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:

  1. Male or female
  2. Age between 18 - 50 years old
  3. 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.
  4. The participants will be able to follow instructions.
  5. Good communication and cooperation.

Exclusion Criteria:

  1. A history of the following diseases or disorders:

    • Rotator cuff disease
    • Cervical radiculopathy
    • Degenerative shoulder joint disease
    • Shoulder stiffness
  2. 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.

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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