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Clinical Trials/NCT02067598
NCT02067598
Completed
Not Applicable

Effects of Scapular Exercise on Patients With Scapulocostal Syndrome

Mae Fah Luang University Hospital1 site in 1 country36 target enrollmentJanuary 2014
ConditionsScapular Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Scapular Pain
Sponsor
Mae Fah Luang University Hospital
Enrollment
36
Locations
1
Primary Endpoint
Pressure Pain Threshold as a measure by algometry
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The purpose of this study is to determine the effect of scapular exercise on pain related parameters including pain intensity, 24 hours pain intensity, pressure pain threshold, anxiety and muscle tension in patients with scapulocostal syndrome.

Registry
clinicaltrials.gov
Start Date
January 2014
End Date
May 2014
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Mae Fah Luang University Hospital
Responsible Party
Principal Investigator
Principal Investigator

Dr. Vitsarut Buttagat

Mae Fah Luang University

Mae Fah Luang University Hospital

Eligibility Criteria

Inclusion Criteria

  • Male or female
  • Age between 18 - 50 years old
  • The participants have experienced spontaneous scapular pain 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 (Chatchawan et al., 2005; Tough et al., 2007).
  • 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
  • Adhesive capsulitis of shoulder

Outcomes

Primary Outcomes

Pressure Pain Threshold as a measure by algometry

Time Frame: 6 Weeks

Secondary Outcomes

  • Pain scores on visual analog scale(6 weeks)
  • Anxiety on State Anxiety Inventory(6 weeks)
  • 24 hours pain intensity on Visual analog scale(6 weeks)
  • Muscle tension on visual analog scale(6 weeks)

Study Sites (1)

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