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临床试验/CTRI/2024/05/067719
CTRI/2024/05/067719尚未招募3 期

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 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2024年5月30日最近更新:

试验速览

阶段
3 期
状态
尚未招募
入组人数
30
试验地点
1
主要终点
Functional Disability

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Outcome Assessor Blinded

入排标准

年龄范围
45.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • 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.

排除标准

  • 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.

结局指标

主要结局

Functional Disability

时间窗: Pre and Post Intervention Period (6 week)

次要结局

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

研究者

申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Dr Divya Manghwani

MGM Institute of Physiotherapy, Aurangabad

研究点 (1)

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