- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06716515
Influence of Gender Difference on Knee Proprioception in Non-Specific Low Back Pain Among Young Adults
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Low back pain (LBP) is one of the most common musculoskeletal disorders and the leading causes of disability and work absence globally. LBP notonly causes individual suffering, but also a heavy burden to the society. Despite this, up to 85% patients with LBP cannot be clearly diagnosed and are classified as non-specific LBP (NSLBP). Proprioception plays an important role in the planning of precise and coordinated movements, in maintaining balance and controlling body posture. It also exerts its influence on motor learning and re-education. Proprioception deficit has been identified in people with LBP and it has been suggested that these deficits might be associated with causes and mechanisms of LBP. Although the local investigation of proprioception is important, the proprioceptive deficits due to LBP may not be restricted only to the lumbar region. Anatomical and biomechanical associations between the knee and lower back segments imply that the knee might be adversely affected in patients with LBP.
there is a gap in the literature concerning sex differences in the knee joint proprioception. Although biomechanical and hormonal differences between males and females are suspected to be responsible for increasing this incidence.
Study Type
Enrollment (Estimated)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Forty-one Patients from each gender participated in the study.
- Subject's age ranged from 18-26 years old, with Body Mass Index (BMI) less than 30Kg/m2
- The dominant knees of the subjects (defined as the leg used for kicking) are tested.
- Pain between three and eight using numerical pain rating scale NPRS, and Oswestry Disability Index score less than 20.
- All the subjects sign an informed consent form. 6. able to comprehend and follow the examiner's instructions.
Exclusion Criteria:
- limitation of active and passive knee joint motion.
- clinical signs of an impairment or abnormality in the knee (such as abnormal range of motion, muscle weakness, or malalignment).
- injury to the knee that required medical attention.
- current pain in the knee or previous surgery on the knee.
- not able to understand and follow the commands of the examiner.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Males
Forty-one males will be evaluated using digital inclinometer in an open kinetic chain position.
The JPS testing is conducted in the sitting position without feet floor contact, at a quiet place with closed eyes .
Investigator will perform all the knee joint position sense assessments in the dominant extremity.
The digital inclinometer is stabilized to the middle third of the subjects' leg (15 cm distal from the apex of the fibular head) with a strap.
The starting position of the test is 90° flexion.
The proprioception evaluation angle is defined at 30°.
Participants are asked to extend their tested knee to the target angle of 30° from the initial position (90° knee flexion) then to return to their initial position after 5 seconds in this position ,The participant indicated by saying "YES" when they thought they reach the target, and the reposition accuracy will be measured as the joint position error (JPE) in degrees, as displayed on the digital inclinometer screen
|
Digital inclinometer to assess gender difference in knee repositioning error
|
|
Females
Forty-one females will be assessed the same as group A , Then compare Results To investigate the impact of gender difference on knee proprioception among non specific low back pain young adults
|
Digital inclinometer to assess gender difference in knee repositioning error
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
knee proprioception
Time Frame: up to 4 weeks
|
knee repositioning error is measured by digital inclinometer
|
up to 4 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Functional disability
Time Frame: up to 4 weeks
|
measured by Oswestry disability index (arabic version)
|
up to 4 weeks
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain intensity
Time Frame: up to 4 weeks
|
measured by Numerical rating scale( each subject choose a number from 0 to 10)
|
up to 4 weeks
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
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/012/005429
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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