Effectiveness of Myofascial Release Versus Dynamic Cupping on Pain, Range of Motion and Functional Mobility in Patients with Frozen Shoulder: A Comparative Study
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 48
- 试验地点
- 1
- 主要终点
- 3)Shoulder pain
研究概览
简要总结
Approval for the research work will be obtained from Institutional Ethical committee. The purpose of the study will be explained to each participant and a written informed consent will be taken in a language they understand. Participants will be screened and recruited for the study on the basis of inclusion and exclusion criteria. Participants will be indexed as per their visit in OPD. Participants will be added in group A and group B by simple random sampling. Subjects in Group A, myofascial release in which gross and focused myofascial release technique along with conventional physiotherapy will be given. Subjects in Group B will receive dynamic cupping technique along with conventional physiotherapy.
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 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
- •Patient clinically diagnosed with unilateral frozen shoulder.
- •Stage II frozen shoulder -Age between 40 years to 65 years.
- •Both genders male and female.
排除标准
- •History with major shoulder injury or surgery.
- •Patients with cervical radiculopathy, paresis or other neurological changes in the upper limb on the involved side.
- •Presence of underlying fracture associated inflammatory arthritis.
- •Any psychological disorder likely to interfere with the course or assessment of the intervention process.
- •Uncontrolled diagnosed neurological diseases, immunodeficiency, bleeding disorders and allergies.
- •Acute infections, using anticoagulants, severe cardiac issues, under pacemaker and Hemophillia and similar conditions.
结局指标
主要结局
3)Shoulder pain
时间窗: Pre and Post treatment effect will be assessed at 0 week and after 2 weeks
1)Visual
时间窗: Pre and Post treatment effect will be assessed at 0 week and after 2 weeks
analogue scale
时间窗: Pre and Post treatment effect will be assessed at 0 week and after 2 weeks
(VAS)
时间窗: Pre and Post treatment effect will be assessed at 0 week and after 2 weeks
2)Goniometer
时间窗: Pre and Post treatment effect will be assessed at 0 week and after 2 weeks
and disability
时间窗: Pre and Post treatment effect will be assessed at 0 week and after 2 weeks
index(SPADI)
时间窗: Pre and Post treatment effect will be assessed at 0 week and after 2 weeks
次要结局
未报告次要终点
研究者
Dr Kiran Chandrakant Yadav
Maharashtra Institue of Physiotherapy Latur
