跳至主要内容
临床试验/CTRI/2025/03/083711
CTRI/2025/03/083711尚未招募不适用

Effectiveness of Myofascial Release Versus Dynamic Cupping on Pain, Range of Motion and Functional Mobility in Patients with Frozen Shoulder: A Comparative Study

Maharashtra Institute of Physiotherapy, Latur1 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2025年4月22日最近更新:

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

发起方
Maharashtra Institute of Physiotherapy, Latur
申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Dr Kiran Chandrakant Yadav

Maharashtra Institue of Physiotherapy Latur

研究点 (1)

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