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临床试验/CTRI/2026/03/105439
CTRI/2026/03/105439尚未招募不适用

Effectiveness of Multimodal Physiotherapy Combined with Pain Neuroscience Education on Pain Disability and Quality of Life in Type 2 Diabetes Mellitus Patients with Frozen Shoulder A Randomized Controlled Trial

Dr Shivani Patil1 个研究点 分布在 1 个国家目标入组 88 人开始时间: 2026年3月31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
88
试验地点
1

研究概览

简要总结

This randomized controlled trial aims to evaluate the effectiveness of multimodal physiotherapy combined with pain neuroscience education in patients with Type 2 Diabetes Mellitus having frozen shoulder. The study will compare this combined intervention with standard physiotherapy to determine its effect on pain reduction, functional disability, and quality of life. The findings may help identify an improved rehabilitation approach for managing diabetes-associated frozen shoulder.

研究设计

研究类型
Interventional
分配方式
Other
盲法
Outcome Assessor Blinded

入排标准

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

入选标准

  • Participant provides written informed consent and agrees to voluntary participation in the study.
  • Male and female participants aged 18 to 70 years.
  • Medically diagnosed with Type 2 Diabetes Mellitus.
  • Diagnosed with Frozen Shoulder also known as Adhesive Capsulitis based on the following: Shoulder pain of at least 3 centimeters on the Visual Analog Scale at rest or during activity for more than three months.
  • Restriction in both active and passive shoulder range of motion.
  • Normal shoulder radiographs.
  • Individuals in Phase One or Phase Two of Frozen Shoulder.
  • Vividness of Visual Imagery Questionnaire score between 16 and 48.

排除标准

  • Patients presenting with shoulder dislocation, arthritis, fracture, avascular necrosis, or osteoporosis.
  • History of surgery involving the neck or affected shoulder.
  • Participants who have undergone any treatment such as corticosteroid injection in the shoulder or physiotherapy within the past one year.
  • Douleur Neuropathique Four Questionnaire score of four or more.
  • History of stroke or other neurological disorders affecting upper limb function.
  • Participants with impaired sensation who may be unable to provide appropriate feedback regarding Transcutaneous Electrical Nerve Stimulation intensity.
  • Participants with pacemaker or epilepsy, as these are contraindications for Transcutaneous Electrical Nerve Stimulation.
  • Diagnosed psychiatric illness or cognitive impairment that may interfere with study participation.

研究者

发起方
Dr Shivani Patil
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Shivani Patil

KLE College of Physiotherapy

研究点 (1)

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