Additive effect of repetitive peripheral magnetic stimulation along with exercises on myofascial trigger points, forward head posture and cervical muscle endurance in young adults with text neck syndrome: A randomized control trial

Pinto Eden Sybil Roland1 个研究点分布在 1 个国家目标入组 52 人开始时间: 2026年2月2日最近更新: 2026年1月7日

试验速览

阶段: 不适用
状态: 尚未招募
发起方
入组人数: 52
试验地点: 1

研究概览研究设计入排标准研究者研究点记录与标识符相似试验

研究概览

简要总结

This randomized control trail aims to evaluate the additive effect of repetitive peripheral magnetic stimulation (rPMS) along with exercises on myofascial trigger points, forward head posture, and cervical muscle endurance in young adults with text neck syndrome. Participants will be randomly allocated to receive either rPMS along with a structured exercise program or exercises alone. Outcome measures will include pain intensity, craniovertebral angle, pain pressure threshold, and cervical muscle endurance.

研究设计

研究类型: Interventional
分配方式: Randomized
盲法: Outcome Assessor Blinded

入排标准

年龄范围: 18.00 Year(s) 至 26.00 Year(s)（—）
性别: All

入选标准

•Males and females between 18 to 26 years Screen time of at least 5 hours per day.
•Pain more than 3 months.
•Numeric pain rating scale (NPRS) (mild to moderate pain intensity) At least one Active Myofascial trigger point in one of the upper trapezius muscle (Pain Pressure threshold of 2.90 to 6.54 newtons) Craniovertebral angle(to assess forward head posture) less than 50 degree No medical or physiotherapy treatment in the past 3 months.
•Not presently undergoing medical or physiotherapy treatment for neck pain and shoulder pain.
•No metal implants, pacemakers, Pregnancy (contraindications of rPMS).

排除标准

•Inability to follow study protocol (non-compliance) Metallic Implants (eg cochlear Implants).
•Subjects diagnosed with Neurological Disorders.
•Subjects who are diagnosed with neck or shoulder surgery or fractures.
•Subjects who are diagnosed with Rheumatological or systemic conditions.
•Subjects who received trigger point injection at upper trapezius muscle within the last 6 months.
•Use of muscle relaxants, pain medication in the past 2 weeks.

研究者

发起方

Pinto Eden Sybil Roland

申办方类型

Research institution and hospital

责任方

Principal Investigator

主要研究者

Pinto Eden Sybil Roland

Institute of Physiotherapy, Srinivas university

研究点 (1)

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