Effect of Vibrotherapy in addition to Resistance training exercises on pain, balance, proprioception and disability in patients with Knee Osteoarthritis
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 26
- 试验地点
- 1
- 主要终点
- Visual Analog Scale (VAS)
研究概览
简要总结
Knee osteoarthritis (OA) is a degenerative joint disease marked by cartilage breakdown, synovial inflammation, bone sclerosis, and osteophyte formation. These changes can damage sensory receptors, particularly mechanoreceptors, leading to impaired proprioception. This impairment contributes to balance deficits and increased fall risk. Purpose: The purpose of current study is to determine the effect of local joint vibration therapy on pain, balance, proprioception and disability in patients with Knee Osteoarthritis. Study design will be a Single blinded randomized sham trial. Participants will be recruited on the basis of inclusion and exclusion criteria. Subjects will be randomly allocated into two groups, group 1 and group 2 through computer based random allocation techniques. Group 1 will receive vibration therapy along with resistance training and group2 will receive sham vibration therapy along with resistance training exercises. Pre test and posttest assessment will be done by VAS, CKOAI, Sensamove. Data will be analysed using SPSS software version 20. The findings from the study will help to improve clinical outcomes by enhancing balance, proprioception, and overall functional ability and can ultimately reduce disability and improve quality of life in patients with knee OA.
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 70.00 Year(s)(—)
- 性别
- All
入选标准
- •Both male and female Diagnosed with tibiofemoral knee OA Grades 1,2 and 3 of knee OA according to Kellgren Lawrence Grading system Persistent symptoms in both knees such as pain and stiffness for a period of at least 3 months A minimum pain intensity score of more than 3 on Visual Analog Scale (VAS) Patient ambulatory with no use of any assistive device No any sensory disturbance.
排除标准
- •History of any trauma/injury in previous 6 months Individuals having history of any previous surgery Individuals suffering from central nervous system disease History of DVT, aneurysms, stroke, epilepsy Intellectual limitations and mental performance Individuals suffering from any other musculoskeletal, neurological, cardiopulmonary conditions.
- •Diabetes mellitus, cardiac or respiratory insufficiency, and inability to understand the procedure.
结局指标
主要结局
Visual Analog Scale (VAS)
时间窗: At Baseline and at 4 weeks
Comprehensive Knee Osteoarthritis Index (CKOAI)
时间窗: At Baseline and at 4 weeks
Sensamove (balance and proprioception)
时间窗: At Baseline and at 4 weeks
次要结局
未报告次要终点
研究者
DIKSHITA KABBA
Maharishi Markandeshwar Institute of Physiotherapy and Rehabilitation
