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

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-26
SponsorCairo University

About this trial

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

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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.

Disqualifiers

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.

Trial 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.

Trial design

Design model

Case-control

Time perspective

Cross-sectional

Treatments tested in this trial

  • digital inclinometer

    Device

    Digital inclinometer to assess gender difference in knee repositioning error

Treatment groups

82 Participants
are divided into 2 treatment groups
Group A: Males1 intervention
Group B: Females1 intervention

Trial outcomes

Primary outcomes

1

knee proprioception

knee repositioning error is measured by digital inclinometer

Time frame
up to 4 weeks

Secondary outcomes

1

Functional disability

measured by Oswestry disability index (arabic version)

Time frame
up to 4 weeks

Other outcomes

1

Pain intensity

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

Time frame
up to 4 weeks

Locations

This trial has no locations.

Sponsors and contacts

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