Knee Pain and Lumbar Proprioception in Knee Osteoarthritis Patients
Association Between Knee Pain and Lumbar Proprioception in Patients With Knee Osteoarthritis
1 other identifier
observational
56
1 country
1
Brief Summary
Knee osteoarthritis (KOA), is a chronic degenerative joint pathology with a global prevalence of 22.9% in individuals aged 40 and over. It is a leading cause of disability and poor quality of life worldwide due to musculoskeletal pain and functional limitations. Musculoskeletal pain is the primary patient-reported outcome in patients with osteoarthritis (OA) and a major cause of disability and functional limitations this study was carried to investigate the correlation between knee pain and lumbar proprioception
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started May 2025
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 20, 2025
CompletedFirst Submitted
Initial submission to the registry
January 28, 2026
CompletedFirst Posted
Study publicly available on registry
February 27, 2026
CompletedFebruary 27, 2026
February 1, 2026
6 months
January 28, 2026
February 20, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
proprioception
Joint position error was measured using the Biodex system 3. Before every test, the system was calibrated and stabilized. The patient was placed in a seated compressed posture on the Biodex system chair. Two curved pads on the front of the legs allowed for individual adjustment of the knee blocks, and the patient's feet were supported in a way that they did not touch the floor, both thighs were stabilized by two straps, the pelvic brace was then applied and positioned as far down as possible to press firmly but comfortably against the superior aspect of the proximal thighs. The starting position for each participant was with their spines flexed at a 60° angle. As a "target position" for the individuals to maintain during the testing, the predetermined spinal ROM was set at 60° to 90° lumbar flexion. All subjects. After recording the subjects' absolute error (AE) values relative to the 90-degree target position for all three trials, the mean deviation was calculated
at the baseline (day 1)
Secondary Outcomes (1)
Pain intensity
at the baseline (day 1)
Study Arms (1)
study group
fifty-six individuals of both sexes between the ages of 40 and 60 years with knee osteoarthritis
Interventions
Eligibility Criteria
Between the ages of 40 and 60 years, fifty-six individuals of both sexes were recruited, their BMI ranged from 24.02 to 29.98.
You may qualify if:
- Male and female participants diagnosed with knee osteoarthritis.
- The participants diagnosed with grade one, grade two and grade three knee osteoarthritis.
- Subjects aged form 40-60 years old.
- All the participants complain of knee pain.
- Participants able to understand the commands.
You may not qualify if:
- Experienced serious trauma leading to fractures and dislocations of the spine.
- They have been diagnosed to have spinal deformities such as scoliosis, lumbar disc herniation and lumbar spondylolisthesis.
- They have infection/malignant spinal conditions. 4- They have cauda equine syndrome. 5- Anyone with psychological disorders (e.g. dementia or drug abuse). 6- Uncooperative participant 7- Anyone with grade four knee osteoarthritis
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
Study Sites (1)
Physical therapy College - Cairo university
Cairo, Egypt
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Target Duration
- 4 Weeks
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant professor of physical therapy
Study Record Dates
First Submitted
January 28, 2026
First Posted
February 27, 2026
Study Start
May 1, 2025
Primary Completion
November 1, 2025
Study Completion
December 20, 2025
Last Updated
February 27, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share