Effects of Scapular Exercise on Patients With Scapulocostal Syndrome
1 other identifier
interventional
36
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jan 2014
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2014
CompletedFirst Submitted
Initial submission to the registry
February 18, 2014
CompletedFirst Posted
Study publicly available on registry
February 20, 2014
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2014
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2014
CompletedMay 6, 2015
May 1, 2015
4 months
February 18, 2014
May 5, 2015
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Pressure Pain Threshold as a measure by algometry
6 Weeks
Secondary Outcomes (4)
Pain scores on visual analog scale
6 weeks
Muscle tension on visual analog scale
6 weeks
Anxiety on State Anxiety Inventory
6 weeks
24 hours pain intensity on Visual analog scale
6 weeks
Study Arms (2)
Scapular exercise
EXPERIMENTALThe participants will receive thirty minutes session of scapular exercise for 12 sessions
Control
NO INTERVENTIONInterventions
Eligibility Criteria
You may qualify if:
- 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.
You may not qualify if:
- \. A history of the following diseases or disorders:
- Rotator cuff disease
- Cervical radiculopathy
- Degenerative shoulder joint disease
- Adhesive capsulitis of shoulder
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
School of Health Science, Mae Fah Luang University
Mueang, Changwat Chiang Rai, 57100, Thailand
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Mae Fah Luang University
Study Record Dates
First Submitted
February 18, 2014
First Posted
February 20, 2014
Study Start
January 1, 2014
Primary Completion
May 1, 2014
Study Completion
May 1, 2014
Last Updated
May 6, 2015
Record last verified: 2015-05