- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02437266
Effect of Scapular Mobilization on Patients With Scapular Pain
May 6, 2015 updated by: Dr. Vitsarut Buttagat, Mae Fah Luang University Hospital
Effect of Scapular Mobilization on Patients With Scapular Pain Associated With Myofascial Trigger Point
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:
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
38
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
-
-
Chiang Rai
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Mueang, Chiang Rai, Thailand, 57100
- School of Health Science, Mae Fah Luang 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
18 years to 50 years (ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
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
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
- Masking: DOUBLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Scapular mobilization
The participants will receive a twenty minutes session of scapular mobilization onto the scapular
|
|
|
NO_INTERVENTION: Control
Rest on the bed for twenty minutes
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
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.
|
5 weeks
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Anxiety on State Anxiety Inventory
Time Frame: 5 weeks
|
5 weeks
|
|
Pressure Pain Threshold as a measure by pressure algometry
Time Frame: 5 weeks
|
5 weeks
|
|
Scapular range of motion
Time Frame: 5 weeks
|
5 weeks
|
|
Patient satisfaction level
Time Frame: 5 weeks
|
5 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
May 1, 2015
Primary Completion (ANTICIPATED)
August 1, 2015
Study Completion (ANTICIPATED)
August 1, 2015
Study Registration Dates
First Submitted
May 5, 2015
First Submitted That Met QC Criteria
May 6, 2015
First Posted (ESTIMATE)
May 7, 2015
Study Record Updates
Last Update Posted (ESTIMATE)
May 7, 2015
Last Update Submitted That Met QC Criteria
May 6, 2015
Last Verified
May 1, 2015
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 55218152-5
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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