NCT02424058
Unknown
Not Applicable
The Investigation of the Sagittal Thoracic Spinal Curvature and Mobility in Subjects With and Without Chronic Neck Pain: Cut-off Points and Pain Relationship
Ataturk Training and Research Hospital1 site in 1 country100 target enrollmentJuly 2014
ConditionsNeck Pain
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Neck Pain
- Sponsor
- Ataturk Training and Research Hospital
- Enrollment
- 100
- Locations
- 1
- Primary Endpoint
- Thoracic curvature, as measured by Spinal Mouse®
- Last Updated
- 11 years ago
Overview
Brief Summary
The purpose of this study is to investigate the sagittal thoracic spinal curvature and mobility in subjects with and without chronic neck pain, cut-off points and pain relationship
Investigators
Seyda TOPRAK CELENAY
Assistant Professor, PT, PhD
Ataturk Training and Research Hospital
Eligibility Criteria
Inclusion Criteria
- •Patients aged between 18 and 65 years with persistent neck pain for more than 3 months
- •The inclusion criteria for the control group included acceptance to participate in the study, no previous neck pain (lifetime-to-date), no spinal surgery or deformity, and no radiological abnormalities detected
Exclusion Criteria
- •Prior history of injury or surgery relating to spine, spinal deformity, neurological symptoms or signs, radiological abnormalities indicating cervical radiculopathy or myelopathy, prior history of other spinal disorder such as low back pain, active intervention in the last 3 months including drug therapy or physiotherapy, malignancy, systemic pathology including any rheumatologic disease and osteoporosis
Outcomes
Primary Outcomes
Thoracic curvature, as measured by Spinal Mouse®
Time Frame: participants will be followed for the duration of hospital stay, an expected average of one year
Secondary Outcomes
- Pain, as measured by Visual Analog Scale(participants will be followed for the duration of hospital stay, an expected average of one year)
- Thoracic mobility, as measured by Spinal Mouse®(participants will be followed for the duration of hospital stay, an expected average of one year)
Study Sites (1)
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