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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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25 May 2015 |
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Main ID: |
NCT02437266 |
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Date of registration:
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05/05/2015 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Effect of Scapular Mobilization on Patients With Scapular Pain
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Scientific title:
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Effect of Scapular Mobilization on Patients With Scapular Pain Associated With Myofascial Trigger Point |
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Date of first enrolment:
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May 2015 |
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Target sample size:
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38 |
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Recruitment status: |
Not yet recruiting |
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URL:
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http://clinicaltrials.gov/show/NCT02437266 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment
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Phase:
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N/A
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Countries of recruitment
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Thailand
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Contacts
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Name:
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Vitsarut Buttagat, Ph.D. |
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Address:
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Telephone:
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66882674423 |
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Email:
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vitsarutbut@hotmail.com |
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Affiliation:
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Name:
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VITSARUT BUTTAGAT, Ph.D. |
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Address:
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Telephone:
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66882674423 |
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Email:
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vitsarutbut@hotmail.com |
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Affiliation:
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Key inclusion & exclusion criteria
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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
Age minimum:
18 Years
Age maximum:
50 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Myofascial Pain Syndrome
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Intervention(s)
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Other: Scapular mobilization
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Primary Outcome(s)
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Pain score on Visual analog scale
[Time Frame: 5 weeks]
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Secondary Outcome(s)
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Anxiety on State Anxiety Inventory
[Time Frame: 5 weeks]
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Scapular range of motion
[Time Frame: 5 weeks]
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Patient satisfaction level
[Time Frame: 5 weeks]
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Pressure Pain Threshold as a measure by pressure algometry
[Time Frame: 5 weeks]
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Secondary ID(s)
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55218152-5
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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