Skip to content

Comparison of effects of two physiotherapy mobilization interventions as an adjunct to institution-based exercise program on pain, joint motion, strength, ability to perform activities of daily living & quality of life in knee osteoarthritis patients

Effects of mobilization with movement vs Maitland joint mobilization as an adjunct to institution-based exercise program on pain, ROM, strength, functional status & quality of life in knee osteoarthritis patients: A randomised clinical trial - Nil

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/066730
Enrollment
68
Registered
2024-05-03
Start date
Unknown
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Health Condition 1: M179- Osteoarthritis of knee, unspecified

Interventions

Intervention1: mobilization with movement and institution-based exercise program: The experimental group A will receive the mobilization with movement for knee joint and institution-based exercise pro

Sponsors

Sancheti Institute for Orthopaedics and Rehabilitation College of Physiotherapy
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Subjects of either gender with an age group of 40-75yrs & having knee pain. 2.Subjects fulfilling American College of Rheumatology clinical criteria. At least one of the following three Age more than 50, morning stiffness less than 30 min, Crepitus on knee motion, with or without X Ray findings. 3.Subjects with grade I to III knee osteoarthritis on the Kellgren and Lawrence scale. 4.Subjects able to stand and walk without help.

Exclusion criteria

Exclusion criteria: 1.Subjects with history of knee/ lower limb joint replacement surgery. 2.Subjects present with history of any lower limb fracture or ligament injury. 3.Subjects with post-traumatic knee osteoarthritis. 4.Subjects with patellofemoral arthritis.

Design outcomes

Primary

MeasureTime frame
1.VAS (Pain) 2.Universal goniometerTimepoint: At baseline (0 weeks) and Post-intervention (4 weeks)

Secondary

MeasureTime frame
Time up and goTimepoint: At baseline (0 weeks) and Post-intervention (4 weeks);30s chair stand testTimepoint: At baseline (0 weeks) and Post-intervention (4 weeks);WOMAC CRD PuneTimepoint: At baseline (0 weeks) and Post-intervention (4 weeks);Micro FET3Timepoint: At baseline (0 weeks) and Post-intervention (4 weeks);WHOQOL-BREFTimepoint: At baseline (0 weeks) and Post-intervention (4 weeks)

Countries

India

Contacts

Public ContactDr Venu Mohan D

Sancheti Institute for orthopaedics and Rehabilitation College of Physiotherapy

venumohan@gmail.com9440690707

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026