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NCT Number: NCT06716515

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

the aim of the study is to investigate the impact of gender difference on knee proprioception among non specific low back pain young adults.

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Key information

Age range

18 year–26 year

Sex eligibility

All sexes

Study type

Observational

About this study

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.

Who can participate

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

digital inclinometer

Device

Digital inclinometer to assess gender difference in knee repositioning error

Primary outcomes

  1. knee proprioception

    Time frame: up to 4 weeks

    knee repositioning error is measured by digital inclinometer

Secondary outcomes

  1. Functional disability

    Time frame: up to 4 weeks

    measured by Oswestry disability index (arabic version)

Other outcomes

  1. Pain intensity

    Time frame: up to 4 weeks

    measured by Numerical rating scale( each subject choose a number from 0 to 10)

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Registry information

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Dec 4, 2024
Registry last updated
Dec 5, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.