Hypermobility Syndrome Clinical Trial
Official title:
Assistant Professor
Verified date | August 2016 |
Source | Ataturk Training and Research Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | Turkey: Ethics Committee |
Study type | Interventional |
The aim of this study is to investigate the effects of an 8-week lumbar spinal stabilization exercise program on pain, trunk muscle endurance and postural stability in women with benign joint hypermobility syndrome
Status | Completed |
Enrollment | 38 |
Est. completion date | October 2015 |
Est. primary completion date | July 2015 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 30 Years |
Eligibility |
Inclusion Criteria: - volunteers in an age range of 18 to 30, - being women, - having benign joint hypermobility syndrome diagnosed according to the Brighton criteria, - having no contraindication to join an exercise program. Exclusion Criteria: - having rheumatologic or neurologic diseases, - any other pathology involving the musculoskeletal system-history of fractures, joint dislocations, sprains and strains, - associated connective tissue disorders including Marfan syndrome, Ehlers-Danlos syndrome, osteogenesis imperfecta, - severe psychological disorders, - being pregnant, - intervention including exercise or physical therapy in the last 3 months. |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Investigator, Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Ataturk Training and Research Hospital |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in musculoskeletal pain intensity as measured by Visual Analog Scale | Change from baseline musculoskeletal pain intensity at 8 weeks | Yes | |
Secondary | Change in trunk muscle endurance as measued with McGill's trunk muscle endurance tests | Change from baseline trunk muscle endurance at 8 weeks | Yes | |
Secondary | Change in postural stability as measured with Biodex Balance System SD | Change from baseline postural stability at 8 weeks | Yes |
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