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Effect of Exercises and Electrical Stimulation in Patients with Knee Osteoarthritis

Effect of Neuromuscular Exercises and Neuromuscular Electrical Stimulation in Patients with Knee Osteoarthritis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/06/034213
Enrollment
120
Registered
2021-06-14
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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: Neuromuscular Exercises: Neuromuscular Exercises with conventional treatment for thrice a week for six weeks Intervention2: Neuromuscular Electrical Stimulation: Neuromuscular electrica

Sponsors

Guru Jambheshwar University of Science and Technology Hisar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Subjects fulfilling American College of Rheumatology (ACR) criteria for knee osteoarthritis 2.Grade II and III knee osteoarthritis as per Kellgren and Lawrence grading system

Exclusion criteria

Exclusion criteria: 1.History of inflammatory and infectious conditions of knee joint 2.Patients with history of surgery around knee joint 3.History of trauma in knee joint 4.Any muscular, joint and neurological conditions affecting lower extremity 5.Unable to walk unaided 6.Currently undertaking any exercise program for knee OA 7.Any contraindication to electrical stimulation (eg. epilepsy) 8.Presence of any skin disorders around knee 9.Any condition or reason restricting the participation of the patient in the study 10.Unwilling and uncooperative patients 11.Patients who have been referred for joint replacement

Design outcomes

Primary

MeasureTime frame
1.Visual Analogue Scale 2.Knee Injury and Osteoarthritis Outcome Score 3.Community balance and mobility scale 4.Dynamic Gait test 5.Range of Motion (ROM) Timepoint: At the baseline At the end of 6 weeks After follow up of 4 weeks weeks.

Secondary

MeasureTime frame
Timed up and go testTimepoint: At the baseline At the end of 6 weeks After follow up of 4 weeks.

Countries

India

Contacts

Public ContactJyoti

Guru Jambheshwar University of Science and Technology Hisar

jyotisabharwal35@gmail.com9416665373

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 6, 2026