Influence of Gender Difference on Knee Proprioception in Non-Specific Low Back Pain Among Young Adults

December 3, 2024 updated by: Norhan Yousif Allam, Cairo University
the aim of the study is to investigate the impact of gender difference on knee proprioception among non specific low back pain young adults.

Study Overview

Status

Not yet recruiting

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

Observational

Enrollment (Estimated)

82

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

N/A

Sampling Method

Probability Sample

Study Population

Eighty-two Young Adults (include males and females), ranging in age from 18 to 26, will be included in the study. Individuals will be assigned into 2 groups. Group (A) 41 males with non specific low back pain (B) 41 females with non specific low back pain.

Description

Inclusion Criteria:

  1. Forty-one Patients from each gender participated in the study.
  2. Subject's age ranged from 18-26 years old, with Body Mass Index (BMI) less than 30Kg/m2
  3. The dominant knees of the subjects (defined as the leg used for kicking) are tested.
  4. Pain between three and eight using numerical pain rating scale NPRS, and Oswestry Disability Index score less than 20.
  5. All the subjects sign an informed consent form. 6. able to comprehend and follow the examiner's instructions.

Exclusion Criteria:

  1. limitation of active and passive knee joint motion.
  2. clinical signs of an impairment or abnormality in the knee (such as abnormal range of motion, muscle weakness, or malalignment).
  3. injury to the knee that required medical attention.
  4. current pain in the knee or previous surgery on the knee.
  5. not able to understand and follow the commands of the examiner.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

December 1, 2024

Primary Completion (Estimated)

February 1, 2025

Study Completion (Estimated)

February 15, 2025

Study Registration Dates

First Submitted

November 29, 2024

First Submitted That Met QC Criteria

November 29, 2024

First Posted (Actual)

December 4, 2024

Study Record Updates

Last Update Posted (Estimated)

December 5, 2024

Last Update Submitted That Met QC Criteria

December 3, 2024

Last Verified

December 1, 2024

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

No

Studies a U.S. FDA-regulated device product

No

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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