NCT07436897

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
56

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started May 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 1, 2025

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2025

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 20, 2025

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

January 28, 2026

Completed
1 month until next milestone

First Posted

Study publicly available on registry

February 27, 2026

Completed
Last Updated

February 27, 2026

Status Verified

February 1, 2026

Enrollment Period

6 months

First QC Date

January 28, 2026

Last Update Submit

February 20, 2026

Conditions

Keywords

knee painOsteoarthritisLumbar proprioceptionRepositioning error.

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

Other: porprioception

Interventions

The Biodex system 3 was used to measure joint position error.

study group

Eligibility Criteria

Age40 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)
Sampling MethodProbability Sample
Study Population

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

Study Sites (1)

Physical therapy College - Cairo university

Cairo, Egypt

Location

MeSH Terms

Conditions

Osteoarthritis

Condition Hierarchy (Ancestors)

ArthritisJoint DiseasesMusculoskeletal DiseasesRheumatic Diseases

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

Locations