临床试验/CTRI/2024/05/067997

CTRI/2024/05/067997招募中2 期

Isolation effect of Functional Magnetic Stimulator (FMS) on Myofascial Pain Syndrome (MPS).

School Of Physiotherapy Delhi Pharmaceutical Science And Research University1 个研究点分布在 1 个国家目标入组 54 人开始时间: 2024年6月3日最近更新: 2024年5月29日

试验速览

阶段: 2 期
状态: 招募中
发起方
入组人数: 54
试验地点: 1
主要终点: Reduce pain and improvement in range of motion.

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

The study will compare two group for pain relief. Both groups will receive treatment for 3 days per week for 3 weeks.

For subjects receiving Functional Magnetic Stimulation (FMS) will be delivered using the super inductive stimulator (The BTL-6000 Super Inductive System, by BTL Industries Ltd.) for 10 minutes with an acute analgesic protocol.
For subjects receiving conventional treatment will include hot fomentation for 10 minutes, stretching of the trapezius muscle, and continuous ultrasound therapy at 1 MHz and 1.2 W/cm2.

研究设计

研究类型: Interventional
分配方式: Randomized
盲法: Participant Blinded

入排标准

年龄范围: 18.00 Year(s) 至 45.00 Year(s)（—）
性别: All

入选标准

•In order to participate in the study, individuals must experience both an active trigger point in the upper trapezius muscle and mechanical pain in the cervical region that has lasted for less than three months.
•Additionally, the pain intensity in the neck and cervical regions should be moderate, ranging from 3 to 8 on a Visual Analogue Scale (VAS) taken within the past 30 days, and the Neck Disability Index score should fall between 15 and 34 (inclusive).

排除标准

•Individuals with the following conditions will be excluded from the study: radicular syndrome (pain radiating down the arm), whiplash injury, or any diagnosed cervical pathology like a herniated disc.
•Additionally, those currently receiving treatment for neck or shoulder pain, using pain medication (analgesics, anti-inflammatory drugs, muscle relaxants), anticoagulant medications, or having a history of psychological/psychiatric conditions, active cancer, or who have undergone invasive spinal procedures within the last 4-6 months will not be eligible to participate.

结局指标

主要结局

Reduce pain and improvement in range of motion.

时间窗: Baseline | After 3 weeks

次要结局

Improvement in functional mobility.(Baseline)

研究者

发起方

School Of Physiotherapy Delhi Pharmaceutical Science And Research University

申办方类型

Research institution

责任方

Principal Investigator

主要研究者

Dr. Shilpa Jain

Delhi Pharmaceutical Science And Research University

研究点 (1)

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