Comparative Efficacy of Kinesio Taping and Sham Taping on Pain and Functional Mobility in patients with Knee Osteoarthritis: A Randomized Controlled Trial
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
- 1. Pain intensity by -Numerical Pain Rating Scale (NPRS).
研究概览
简要总结
PURPOSE OF THE STUDY:
There are various studies showing efficacy of Kinesio Taping in patients with Knee Osteoarthritis in Pain, Gait, Strength, Proprioception and Balance etc. However, to the best of our knowledge there are no studies which compared the efficacy of Kinesio Taping and Sham Taping on Pain and Functional Mobility in patients with Knee Osteoarthritis in Indian population.
Therefore, the purpose of the study is to find out the comparative efficacy of Kinesio Taping and Sham Taping on Pain and Functional Mobility in patients with Knee Osteoarthritis.
AIM:
To compare the efficacy of Kinesio Taping and Sham Taping on pain and functional mobility in patients with Knee Osteoarthritis.
OBJECTIVES:
1. To find out the efficacy of Kinesio Taping along with Standardized Exercise Programon pain and functional mobility in patients with Knee Osteoarthritis.
2. To find out the efficacy of Sham Taping along with Standardized Exercise Program on pain and functional mobility in patients with Knee Osteoarthritis.
3. To compare the efficacy of Kinesio Taping and Sham Taping along with Standardized Exercise Program on pain and functional mobility in patients with Knee Osteoarthritis.
NULL HYPOTHESIS :
There is no statistically significant difference between the efficacy of Kinesio Taping and Sham Taping on pain and functional mobility in patients with Knee Osteoarthritis.
ALTERNATIVE HYPOTHESIS :
There is statistically significant difference between the efficacy of Kinesio Taping and Sham Taping on pain and functional mobility in patients with Knee Osteoarthritis.
PROCEDURE:
Institutional Ethical Committee (IEC) approval will be taken before commencement of the study. All patients having Knee Pain or diagnosed with Knee Osteoarthritis are referred to the department of Physiotherapy from the Assessment clinic (ASC) of National Institute for Locomotor Disabilities (Divyangjan) will be approached with the proposal of the study. Total 30 patients will be evaluated and screened according to inclusion and exclusion criteria along with radiological evaluation using x-ray for Kellgren and Lawrence classification .Patients meeting the exclusion criteria will not be included. Those fulfilling the inclusion criteria will be explained in details about the study in their preferred language. Written informed consent will be obtained from the patients agreeing to participate. Then the patients will be randomly divided into two groups by block randomization method by computer generated random blocks.
The demographic data and the outcome measure for Pain Intensity by Numerical Pain Rating Scale (NPRS), Functional Mobility by Timed Up and Go (TUG) Test and Function by WOMAC Osteoarthritis Index will be collected from each patient at Day 1 before starting the intervention and post-intervention at Day 10 i.e.at the end of 10th session (5 sessions per week for 2 weeks). All the patients in “Group A†(n=15) will be treated with Kinesio Taping along with Standardized Exercise Program for 10 sessions, whereas in “Group B†(n=15) patients will be treated with Sham Taping along with Standardized Exercise Program for 10 sessions.
Kinesio Taping and Sham Taping will be applied 4 sessions for 2 weeks on 1st ,3rd ,5th & 8th day and Standardized Exercise Program for 5 sessions per week for 2 weeks. The patient will be advised to contact the investigator incase the tape is dislodged or separated from the skin. After completion of 10 sessions (5 sessions per week) of intervention, all the patients will continue Home Exercise Program (HEP).
Rescue medication duly prescribed by the physician will be continued throughout the study, along with the standardized physiotherapeutic approach in both the groups.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- Participant Blinded
入排标准
- 年龄范围
- 40.00 Year(s) 至 65.00 Year(s)(—)
- 性别
- All
入选标准
- •Both male and female patients willing to participate.
- •Patients aged between 40-65 years.
- •Pain duration of more than 3 months.
- •Numerical Pain Rating Scale (NPRS) Score between 3-
- •Patients with Knee Osteoarthritis grade III according to Kellgren and Lawrence classification.
排除标准
- •History of acrylic allergy or positive patch test.
- •Active localised skin infection, irritated or fragile skin around the knee, open traumatic wound, recent scars.
- •Musculoskeletal conditions like ligament sprains, meniscus injury, fracture, any surgery of lower extremity and deformity of lower extremities etc.
- •Rheumatological diseases like rheumatoid arthritis and ankylosing spondylosis or any infective arthritis.
- •Systemic disorders involving lower extremity like deep vein thrombosis, venous insufficiency and lymphatic disorders etc.
- •Diagnosed neurological conditions like stroke, cerebral palsy, muscle dystrophies, peripheral neuropathies, spinal cord and brain injury etc.
- •Patients who are using knee orthosis.
- •Non-cooperative patients.
结局指标
主要结局
1. Pain intensity by -Numerical Pain Rating Scale (NPRS).
时间窗: 2 times - on day 0 and after 2 weeks (10 sessions)
2. Functional mobility by - Timed Up and Go (TUG) Test.
时间窗: 2 times - on day 0 and after 2 weeks (10 sessions)
3. Function by - WOMAC Osteoarthritis Index.
时间窗: 2 times - on day 0 and after 2 weeks (10 sessions)
次要结局
未报告次要终点
研究者
Aida Priyanka
National Institute For Locomotor Disabilities(Divyangjan)
