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Comparison Of Maitland Mobilisation With Two Different Physiotherapy Treatment Approaches for Pain, Function and Quality of Life in Postmenopausal Women with Bilateral Knee Osteoarthritis

A Comparative Study Of Maitland Mobilisation Combined With Multimodal Physiotherapy Approaches On Pain, Function and Quality of life In Postmenopausal Women With Bilateral Knee Osteoarthritis - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/101761
Enrollment
60
Registered
2026-01-21
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: M170- Bilateral primary osteoarthritis of knee

Interventions

Intervention1: Maitland Mobilisation with Interferential current therapy, Multiple-angle isometrics and Step-up and Step down exercise: Participants will receive Maitland mobilisation grade II and III

Sponsors

Sehajleen Kaur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Postmenopausal women 2. Radiologically diagnosed bilateral knee osteoarthritis (Kellgren-Lawrence grade II -III) (Radiograph obtained within six months of the outset of the study) 3. Persistent knee pain present for more than 3 months

Exclusion criteria

Exclusion criteria: 1. History of knee surgery or intra-articular injection within the last 6 months 2. Advanced Osteoarthritis (Kellgren -Lawrence grade IV) 3. Neurological disorders affecting gait or balance 4. Rheumatoid arthritis 5. Acute trauma, fracture or ligamentous injury of the lower limb 6. Concurrent participation in another physiotherapy or exercise trial

Design outcomes

Primary

MeasureTime frame
1. Numeric Rating Scale 2. Western Ontario and McMaster Universities Osteoarthritis Index 3. World Health Organization Quality of Life BREF (Brief Version)Timepoint: 1. Baseline and Post-intervention (4 weeks) 2. Baseline and Post-intervention (4 weeks) 3. Baseline and Post-intervention (4 weeks)

Secondary

MeasureTime frame
1. Universal Goniometer 2. Manual Muscle TestingTimepoint: 1. Baseline and Post-intervention (4 weeks) 2. Baseline and Post-intervention (4 weeks)

Countries

India

Contacts

Public ContactRishamdeep Kaur

Khalsa College, Amritsar

risham3650@gmail.com9855972227

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026