跳至主要内容
临床试验/CTRI/2025/09/094826
CTRI/2025/09/094826尚未招募不适用

Effects of Proprioceptive Neuromuscular Facilitation and Capsular Stretching with Rotator Cuff Strengthening Exercise for Patients with Adhesive Capsulitis.

Dr Ehsanur Rahman1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2025年10月1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
30
试验地点
1
主要终点
Primary Outcome: Numeric Pain Rating Scale(NPRS)for pain

研究概览

简要总结

This study aims to evaluate the effects of Proprioceptive Neuromuscular Facilitation (PNF), capsular stretching, and rotator cuff strengthening exercises on reduce  pain, improve muscle strength,and shoulder range of motion in adults aged 25-70 years diagnosed with unilateral adhesive capsulitis. Participants will undergo a 6-week intervention program with four sessions per week, each lasting 45-60 minutes. Primary Outcome  include pain  (NPRS), Secondary outcome include strength (MMT), ROMby  Goniometer assessments, and Shoulder Disability (SPDI). The study is designed as a non-randomized clinical trial conducted at the Department of Physiotherapy and Rehabilitation, Jashore University of Science and Technology (JUST) and the Centre for the Rehabilitation of the Paralysed (CRP), Savar. This research aims to provide evidence-based physiotherapy protocols to improve shoulder function and reduce pain in patients with adhesive capsulitis.

研究设计

研究类型
Interventional
分配方式
Na
盲法
None

入排标准

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

入选标准

  • Clinically diagnosed with unilateral adhesive capsulitis based on Cyriax capsular pattern concept by a qualified physiotherapist.
  • Duration of shoulder pain between 1 to 3 months.

排除标准

  • A history of using drugs due to adhesive capsulitis and surgery on the shoulder or manipulation under anesthesia.
  • Neurologic deficits affecting shoulder function during ADL or diagnosed as brachial plexopathy by nerve conduction study (NCS) Pain or disorders of the cervical spine, elbow, wrist or hand.
  • Other conditions involving the shoulder as rotator cuff tear or tendinitis, etc.

结局指标

主要结局

Primary Outcome: Numeric Pain Rating Scale(NPRS)for pain

时间窗: 6 weeks

次要结局

  • Secondary Outcome: Goniometer for AROM/PROM measure, Shoulder Pain and Disability Index (SPDI) for functional activities, Manual Muscle Testing (MMT) for rotator cuff strength.

研究者

发起方
Dr Ehsanur Rahman
申办方类型
Other [Public University]
责任方
Principal Investigator
主要研究者

Md Naim Asrafi

Jashore University of Science and Technology

研究点 (1)

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