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Integrated Trunk Stabilization With Osteoarthritis Rehabilitation in Knee-Spine Syndrome

Integrating Trunk Stabilization Exercises With Conventional Rehabilitation Protocol for Osteoarthritis in Patients With Knee-Spine Syndrome

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07484594
Enrollment
70
Registered
2026-03-20
Start date
2026-05-11
Completion date
2026-10-15
Last updated
2026-07-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Knee Osteoarthritis

Keywords

Knee Osteoarthritis, Knee-Spine Syndrome, Trunk Exercise

Brief summary

This study aims to evaluate the effects of integrating trunk stabilization exercises with conventional rehabilitation in patients with knee-spine syndrome. It further examines whether improving trunk stability can reduce knee pain and enhance functional outcomes in knee osteoarthritis

Detailed description

This study aims to evaluate the effects of integrating trunk stabilization exercises with conventional rehabilitation protocols for patients with knee-spine syndrome. It seeks to determine whether improving trunk stability can positively influence knee joint mechanics, leading to a reduction in knee pain and improvements in physical function, mobility, and overall functional performance in individuals with knee osteoarthritis. The findings may support a more comprehensive rehabilitation approach addressing both spinal and knee involvement in osteoarthritis management.

Interventions

OTHERTrunk Stabilization exercises with conventional Rehab

The protocol for will be followed for 6 weeks, where individuals will perform trunk stabilization exercises with conventional rehabilitation for knee osteoarthritis.

OTHERConventional Rehabilitation

The protocol for will be followed for 6 weeks, where conventional rehabilitation for knee osteoarthritis will be implemented.

Sponsors

Riphah International University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
40 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Age 40-60 years * Both Genders * Bilateral Knee osteoarthritis diagnosed according to the American College of Rheumatology Clinical Classification system * Kellgren \& Lawrence grade 2 and 3 with complaint of pain, crepitations, stiffness and bony enlargement * History of backpain for the past 3 months with no complaint of radiating pain * Able to walk independently/unaided

Exclusion criteria

* Kellgren \& Lawrence grade 4 * Intra-articular corticosteroid injections in the last 3 months or hyaluronic knee injection in the previous 6 months. * History of lower limb or lumbar trauma/surgery, presence of fracture or deformity, or planned surgery within the study period * Lumbar pathologies, for example, spondylolisthesis, ankylosing spondylitis, or any diagnosed severe cardiovascular, pulmonary, neurological, or psychological disease or impairment except lumbar spondylosis * BMI\>30 * Presence of infection, cauda equina syndrome, or meningitis

Design outcomes

Primary

MeasureTime frameDescription
Visual Analogue Scale6 weeksThe Visual Analog Scale (VAS) is a simple and reliable tool for assessing pain intensity on a continuous visual scale. The extreme limits of pain are represented by the straight line's ends, where 0 indicates no pain, and 10 indicates the worst pain a person has ever felt.
Western Ontario and McMaster Universities Arthritis Index (WOMAC)6 weeksIt is widely used in the evaluation of knee osteoarthritis to assess activities of daily living, functional mobility, gait, general health, and quality of life. It has 24 items divided into 3 subscales: pain (5 items), stiffness (2 items), and physical function (17 items). The scores range from 0 to 4 for each subscale. The score ranges from 0 to 96, where zero indicates no pain, stiffness, and functional limitation. Higher scores indicate worse pain, stiffness, and functional limitation.

Secondary

MeasureTime frameDescription
Range Of motion (ROM)6 weeksA Goniometer is used to measure active and passive ROM for knee flexion and extension while the patient lies supine
Time-Up-and-Go (TUG)6 weeksThis test is a widely used assessment of functional mobility, particularly in patients with knee osteoarthritis. The test measures the total time it takes for a patient to stand up from a chair, walk 3 meters at a comfortable pace, turn around, walk back to the chair, and sit down. A shorter time indicates better functional performance
Oswestry Disability Index (ODI)6 weeksIt is a questionnaire that gives a subjective percentage score of level of function/disability in activities of daily living of patients with low back pain. It contains 10 items, each scored from 0 to 5, with the total score converted to a percentage ranging from 0% to 100%. Higher percentages indicate greater disability, i.e., worse outcomes, while lower percentages indicate less disability/better outcomes.
Flexicurve (Lumbar Range of motion)6 weeksFlexicurve is a flexible plastic-coated metal ruler molded to the lumbar spine's sagittal contour (typically T12 to S1) to non-invasively measure lordosis angle via traced perpendicular heights, serving as a radiation-free alternative to X-rays

Countries

Pakistan

Contacts

CONTACTSuman Sheraz, PhD
suman.sheraz@riphah.edu.pk03335646361
CONTACTImran Amjad, PhD
imran.amjad@riphah.edu.pk03324390125
PRINCIPAL_INVESTIGATORSuman Sheraz, PhD

Riphah International University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 21, 2026