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临床试验/CTRI/2024/10/075807
CTRI/2024/10/075807已完成不适用

To Compare the Effect of Resistance Training With Theraband Versus Conventional Exercise on Pain And Quality Of Life of the Patient with Knee OA

Ira Pandey1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2024年11月15日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
30
试验地点
1
主要终点
VAS Scale

研究概览

简要总结

The eligibility of the candidate will be taken from the basis of inclusion criteria.

30 subjects will be randomly selected and then consent form will be filled by eligible candidates after this they will be randomly allotted in these 2 groups .

GROUP A – Resistance training with theraband Patients will be given conventional exercises according to American Academy of Orthopedic Surgeons [AAOS] guidelines and protocol for knee conditioning which will include knee extension, pelvic abduction , leg- press exercise. These patient will attend the intervention program 10 times for 45 minutes per day for 4 weeks.

GROUP B- Conventional Exercises Patients will be given conventional exercises according to American Academy of Orthopedic Surgeons [AAOS] guidelines and protocol for knee conditioning which will include using sand bag for static quadriceps exercise, U/L straight leg raise exercise in supine , U/L hamstring stretching exercises, Hip abduction strengthening exercise , Hip adduction strengthening exercise ,U/L straight leg raise exercise in prone, Knee extension exercise, Calf raise exercise, Ankle pump. These patient will attend the intervention program 10times for 45 minutes per day for 4weeks

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
Participant and Outcome Assessor Blinded

入排标准

年龄范围
40.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • 1.Not involved in any physiotherapy treatment 2.Patient is willing to participate 3.Patient is able to follow all the commands.

排除标准

  • 1.Inability to walk
  • Unstable Heart Conditions
  • Going to participate in another physical activity program
  • Epilepsy 5.Previous knee arthroplasty
  • Previous traumatic history 7.

结局指标

主要结局

VAS Scale

时间窗: 4 weeks

Goniometer

时间窗: 4 weeks

次要结局

  • VAS Scale

研究者

发起方
Ira Pandey
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Ira Pandey

Mahatma Gandhi University of Medical Sciences and Technology

研究点 (1)

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