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Clinical Trials/CTRI/2024/05/067719
CTRI/2024/05/067719
Not yet recruiting
Phase 3

Effectiveness of Patellar Tendon Loading Exercises on Functional Disability, Pain and Electromyographic Activity of Quadriceps Muscle in Patients with Knee Osteoarthritis - A Pilot Randomized Controlled Trial.

MGM Institute of Physiotherapy1 site in 1 country30 target enrollmentStarted: May 30, 2024Last updated:

Overview

Phase
Phase 3
Status
Not yet recruiting
Enrollment
30
Locations
1
Primary Endpoint
Functional Disability

Overview

Brief Summary

Patients with Knee Osteoarthritis will be included in the study trial if they met the inclusion criteria. The written and oral consent of all patients will be taken, and procedure will be explained. Demographic data will be noted. Baseline data which include Functional Disability, pain and Electromyographic Activity of Quadriceps Muscle will be assessed. The patients will be randomly divided into two study groups intervention group and control group. The patients will receive intervention as per the group allocation for 6 weeks. The intervention group will receive Progressive Patellar Tendon Loading Exercises in addition to the conventional physiotherapy whereas the control group will receive conventional physiotherapy only. Patellar Tendon Loading Exercises include progression of 5 exercises (1-Waking to interval jogging, 2-Step ups and Step down, 3-Squats, 4- Lunges, 5-Decline Squats) will be given 3 sessions/week for 6 weeks. Conventional Physiotherapy Includes IFT + Exercises (Isometric quadriceps exercise, Isometric hamstring exercise, Straight leg raising (SLR) exercise, Isometric hip adduction exercise,  Hip abduction exercise, Hip Extension exercise, Dynamic Quadriceps) will be given 3 sessions/week for 6 weeks. All participants will be receiving one session of 30-40 minutes per day. Outcome measures will be assessed pre and post intervention period. Statistical analysis of the collected data will be done. Conclusion will be established based on the obtained results of the study.

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
Outcome Assessor Blinded

Eligibility Criteria

Ages
45.00 Year(s) to 60.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • 1.Patients of both genders.
  • 2.Age group 45-60 years.
  • 3.Patients with Kellgren Lawrence grade 1 and grade 2(Diagnosed Mild OA).
  • 4.Patients with activity related joint pain.
  • 5.Patients with functional difficulty.

Exclusion Criteria

  • 1.Patients with H/O of Knee surgery (Arthroplasty / arthroscopy) or Fracture.
  • 2.Patient received Intra-articular injection in last 3 months.
  • 3.Patient with Diagnosed Osteoporosis grade
  • 4.Patients with systemic conditions like RA.
  • 5.Patients with neurological conditions(Parkinson Disease, stroke).
  • 6.BMI more than 30.

Outcomes

Primary Outcomes

Functional Disability

Time Frame: Pre and Post Intervention Period (6 week)

Secondary Outcomes

  • Pain(Pre and Post Intervention Period (6 week))
  • Electromyographic Activity of Quadriceps Muscle(Pre and Post Intervention Period (6 week))

Investigators

Sponsor Class
Research institution and hospital
Responsible Party
Principal Investigator
Principal Investigator

Dr Divya Manghwani

MGM Institute of Physiotherapy, Aurangabad

Study Sites (1)

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