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临床试验/CTRI/2025/06/089529
CTRI/2025/06/089529尚未招募不适用

Effect of transcranial direct current stimulation with exercises on pain, function and forward head posture in chronic non specific neck pain: A randomised sham controlled trail.

Dr Neha Kulkarni1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年7月18日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
1)Visual analogue scale

研究概览

简要总结

Thirty to fifty percent of people suffer from chronic non-specific neck pain, which is frequently brought on by aspects of modern living including persistent poor posture, especially forward head posture. Disability, a lower quality of life, and trouble with day-to-day functioning are the results of this disorder. Despite being widely used, traditional treatments—such as different strengthening and therapy modalities—frequently have variable results. Through the central pain gate mechanism, transcranial direct current stimulation (tDCS), a new physiotherapy technique, may lessen pain by promoting neuroplasticity and modifying pain perception.There is little and conflicting data about the effectiveness of tDCS for general neck pain, despite early research suggesting it may help with ailments like fibromyalgia, cervicogenic headaches, and low back pain. Therefore, more study is required to examine how tDCS and exercise therapy work together to provide long-lasting pain relief and functional improvement for those with persistent, non-specific neck pain.

60 participants with non specific neck pain will be selected randomly and will be divided into 2 groups(interventional group, sham group). Treatment will be given for 4 weeks,5 days a weeks and outcome measures will be compared pre and post the intervention.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Outcome Assessor Blinded

入排标准

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

入选标准

  • •patients suffering from neck pain for 12 weeks or more and have no specific cause for pain.

排除标准

  • •Pregnant ladies Recent fractures of trauma to neck or upper back.
  • •Recent surgery Severe heart disease, recent heart attack or any issue which restricts the participant from participation in the intervention.
  • •Cervicogenic headache Cervical Radiculopathy.

结局指标

主要结局

1)Visual analogue scale

时间窗: at baseline and after 4 weeks of intervention

2)Copenhagen neck functional disability scale

时间窗: at baseline and after 4 weeks of intervention

3)Kinovea software

时间窗: at baseline and after 4 weeks of intervention

次要结局

未报告次要终点

研究者

发起方
Dr Neha Kulkarni
申办方类型
Research institution and hospital

研究点 (1)

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