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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02869373
Other study ID # 2015-64/82
Secondary ID
Status Completed
Phase Phase 2
First received August 12, 2016
Last updated August 12, 2016
Start date April 2015
Est. completion date October 2015

Study information

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

Clinical Trial Summary

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


Recruitment information / eligibility

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.

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
spinal stabilizaton exercise
In Exercise group, spinal stabilization exercise program was carried out 3 days a week for 8 weeks.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Ataturk Training and Research Hospital

Outcome

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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