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Efficacy of Mulligan rotational taping on pain, knee range of motion, foot posture and gait parameters in knee osteoarthritis- A Randomised Control Trial

Efficacy of Mulligan rotational taping on pain, knee range of motion, foot posture and gait parameters in individuals with medial compartment knee osteoarthritis- A Randomised Control Trial - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/09/057590
Enrollment
50
Registered
2023-09-13
Start date
Unknown
Completion date
Unknown
Last updated
2024-10-14

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

Conditions

Health Condition 1: M171- Unilateral primary osteoarthritisof knee

Interventions

Intervention1: Mulligan rotational taping: Duration: 6 days. An inelastic tape over a underwrap tape will be applied to the leg, starting from the fibular head, by giving a rotational glide and ending

Sponsors

Sancheti Institute for Orthopaedics and Rehabilitation College of Physiotherapy, Pune
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients referred to the physiotherapy department. 2.Patients between age group 50-70 diagnosed radiographically with primary knee Osteoarthritis. 3.Patients diagnosed with stage 2 and 3 on Kellgren-Lawrence scale. 4.Patients with pain intensity on VAS 4 to 8

Exclusion criteria

Exclusion criteria: 1.Patients having any history of trauma to the lower limb in the past 1 year. 2.Patients with any surgical history for the spine or lower limb in the past 1 year. 3.Patients with uncontrolled systemic diseases like Diabetes Mellitus. 4.Patients with any neurological and cardiovascular impairments. 5.Patients with predominant Lateral tibiofemoral compartment or patellofemoral compartment osteoarthritis. 6.Patients with contraindications to manual therapy. 7.Patients having allergic reactions to the tape or having any skin disorders. 8.Patients with BMI > 30kg/m2

Design outcomes

Primary

MeasureTime frame
Pain- using Visual analogue scale Range of motion- using universal goniometer Foot posture- using FPI_6 Gait parameters- using mobile applicationTimepoint: Pre-intervention & 1 week after the intervention

Secondary

MeasureTime frame
Plantar pressure using Podiatech foot platesTimepoint: Pre-intervention & 1 week after the intervention

Countries

India

Contacts

Public ContactDr Nilima Bedekar

Sancheti Institute for Orthopedics and Rehabilitation College of Physiotherapy, Pune

nilimabedekar@yahoo.com9420861882

Outcome results

None listed

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