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.
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
