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Finding the effect of a customized exercise program in improving pain and disability of people with knee arthritis compared to usual exercise program: A randomized controlled study

Investigating the effect of an exercise program in improving pain and disability of people with knee osteoarthritis

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
SLCTR
Registry ID
SLCTR/2022/022
Enrollment
Unknown
Registered
2022-10-07
Start date
2023-02-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Knee osteoarthritis

Interventions

- Study setting – Clinical setting - Randomisation - Is done using a computer generated random number - Intervention - Combined lumbar strengthening program and usual osteoarthritis rehabilitation

Sponsors

None
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • Age 18 years or above 18 years • Fulfills the American College of Rheumatology clinical classification criteria for knee osteoarthritis. In this criteria the presence of knee pain along with at least three of the following six items can classify the condition as knee osteoarthritis: o Age> 50 years old o Morning stiffness < 30 minutes o Crepitus on active knee motion o Bony tenderness o Bony enlargement o No palpable warmth of synovium knee joint osteoarthritis o Less than or equal to grade 2 (as diagnosed and graded by a Rheumatologist, based on the Kellgren and Lawrence radiological classification)

Exclusion criteria

Exclusion criteria: • Hip/Ankle/ Foot osteoarthritis • History of neurological, infectious, and systemic diseases, including cerebrovascular disease, spinal cord disease, spondylitis, cancer, rheumatologic disorders, which may cause long-term immobilization • Participants with structural lesions, such as spondylolisthesis (Lumbar spinous process palpation and stork test) • Vertebral bone fracture, visible significant scoliosis or kyphosis or lower limb radiculopathy (as confirmed by straight leg raise test to exclude radiculopathy from spinal origin) • Knee injection within previous three months • Participants who have prescribed exercise therapy in the past >3 months • Any history of spinal or lower extremity surgery • Pregnancy

Design outcomes

Primary

MeasureTime frame
Measures relate to knee joint Change in the measure and % of the change in, i. Pain intensity: (visual analogue scale (VAS)) ii. Active range of motion (AROM): flexion, extension iii. Disability/function: Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) [Pre-intervention, after 6 weeks post-intervention, after 6 months follow up] Measures relate to lumbar spine Change in the measure and % of the change in, i.Pain intensity: (VAS) ii.AROM: flexion, extension, side-flexion, rotation iii.Disability: Oswestry Disability Index (ODI) [ Pre-intervention, after 6 weeks post-intervention, after 6 months follow up]

Secondary

MeasureTime frame
None []

Countries

Sri Lanka

Contacts

Public ContactPiyumi Amarasinghe

Physiotherapist

dghembilipitiya@gmail.com0472230994

Outcome results

None listed

Source: SLCTR (via WHO ICTRP) · Data processed: Aug 9, 2026