- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04082013
Effect of Opposite Leg Position on Hamstring Flexibility in Patients With Mechanical Low Back Pain
PURPOSE: this study aimed to investigate the effect of opposite knee position on hamstring flexibility BACKGROUND Hamstrings tightness is one of the most common findings in patients with LBP. It is thought that, due to the attachments of hamstrings to the ischial tuberosity, hamstrings tightness generates posterior pelvic tilt and decreases lumbar lordosis, which can result in LBP.
HYPOTHESES There will be significant difference in the hamstring flexibility with changing position of opposite knee (flexed or extended) in patients with mechanical low back pain.
RESEARCH QUESTION: Will changing position of opposite knee (flexed or extended) affect the hamstring flexibility in patients with mechanical low back pain?
Study Overview
Detailed Description
- The subject will be instructed to maintain 90° hip flexion in the supine position.
- Then asked to actively extend the knee joint.
- The degree of achieving active knee extension will be measured using a universal goniometer.
- The average of three active knee extension measurements will be recorded used as the hamstring muscle length for the data analysis (Dong-Kyu Lee, et al., 2018).
- This test will be done for the same limb with opposite leg extended and with opposite flexed.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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Giza, Egypt
- Cairo university
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
- Male and female
- Age range from 18-40 years old
- With previous mentioned inclusion criteria
Description
Inclusion Criteria:
- Patients with history of back pain and assessed with Mechanical inflammatory low back pain index and have very high grade for mechanical component.
- Age ranges from 18-40 years.
- The body mass index of the subject is ≤25 kg/meter square.
Exclusion Criteria:
- Previous trauma, fractures or surgery of the back.
- Malignancy of the back.
- Rheumatoid arthritis
- Spondylolysis or spondylolithesis
- History of lower extremity injury within 6 months prior to the study
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Knee extension ROM
Time Frame: 30 minutes
|
measuring knee extension ROM from 90 degrees hip flexion with opposite-leg flexed and extended
|
30 minutes
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- P.T.REC/012/002301
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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