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临床试验/CTRI/2026/02/103610
CTRI/2026/02/103610尚未招募不适用

Effect of Pulse Electromagnetic Stimulation on Pain and Functional Mobility in Patients with Frozen Shoulder: A Randomized Controlled Trial

Misbah Anjum1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2026年2月25日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
40
试验地点
1
主要终点
Pain intensity will be

研究概览

简要总结

The objective of this randomized controlled trial is to evaluate the therapeutic efficacy of Pulsed Electromagnetic Stimulation (PEMS) as an adjunct to conventional physiotherapy for managing frozen shoulder (adhesive capsulitis). A total of 30 participants will be recruited via convenient sampling and randomly assigned to one of two arms. Group A (Experimental) will receive PEMS in addition to a conventional physiotherapy regimen consisting of range of motion exercises, stretching, and manual therapy. Group B (Control) will receive the conventional physiotherapy regimen alone. The intervention will be administered 3 times per week for a duration of 4 weeks (total 12 sessions). Primary outcomes include pain intensity measured by the Numerical Pain Rating Scale (NPRS), while secondary outcomes include shoulder range of motion via goniometry and functional disability measured by the Shoulder Pain and Disability Index (SPADI). Assessments will be conducted at baseline, weekly, and post-intervention to determine significant differences between the two treatment protocols.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

年龄范围
40.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • •Participants aged between 40 and 60 years.
  • •Both males and females will be included.
  • •Individuals experiencing shoulder pain with limited range of motion.
  • •Participants must be able to comprehend instructions and provide informed consent.

排除标准

  • •• Patients with secondary frozen shoulder resulting from trauma or surgical procedures.
  • •• Individuals having metallic implants or any contraindications to PEMS therapy Those with neurological impairments affecting the upper limb.

结局指标

主要结局

Pain intensity will be

时间窗: 12 sessions across a four-week | period

measured using the Numerical Pain Rating Scale

时间窗: 12 sessions across a four-week | period

(NPRS)

时间窗: 12 sessions across a four-week | period

次要结局

  • Shoulder range of motion will be assessed with a(goniometer, and functional status will be)

研究者

发起方
Misbah Anjum
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Misbah Anjum

Amity University Noida

研究点 (1)

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