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Clinical Trials/NCT02437266
NCT02437266
Unknown
Not Applicable

Effect of Scapular Mobilization on Patients With Scapular Pain Associated With Myofascial Trigger Point

Mae Fah Luang University Hospital1 site in 1 country38 target enrollmentMay 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Myofascial Pain Syndrome
Sponsor
Mae Fah Luang University Hospital
Enrollment
38
Locations
1
Primary Endpoint
Pain score on Visual analog scale
Last Updated
10 years ago

Overview

Brief Summary

The purpose of this study is to determine the effect of scapular mobilization on pain related parameters including pain intensity, pressure pain threshold, muscle tension, anxiety, Scapular range of motion, patient satisfaction in patients with scapular pain associated with myofascial trigger point:

Registry
clinicaltrials.gov
Start Date
May 2015
End Date
August 2015
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

Dr. Vitsarut Buttagat

Mae Fah Luang University Hospital

Eligibility Criteria

Inclusion Criteria

  • 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 muscles surrounding the scapula. 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

  • Shoulder impingement syndrome
  • Adhesive capsulitis
  • Shoulder instability
  • Shoulder arthritides
  • Shoulder dislocation and/or bone fracture
  • Hypermobility of shoulder joint
  • Open wound
  • Drug and/or alcohol intoxication
  • Contraindications of mobilization

Outcomes

Primary Outcomes

Pain score on Visual analog scale

Time Frame: 5 weeks

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.

Secondary Outcomes

  • Pressure Pain Threshold as a measure by pressure algometry(5 weeks)
  • Scapular range of motion(5 weeks)
  • Anxiety on State Anxiety Inventory(5 weeks)
  • Patient satisfaction level(5 weeks)

Study Sites (1)

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