The Effects of Physiotherapy in Migraine
2026年8月25日 更新者：Beyza Avcı、Ankara Yildirim Beyazıt University
The Effects of Physiotherapy Applications in Individuals With Migraine
The aim of this study is to investigate the effects of a physiotherapy program including cervical muscle training and transcutaneous auricular vagus nerve stimulation (taVNS) on pain, functional status, quality of life, psychological status, and sleep quality in individuals with migraine.
研究概览
研究类型
介入性
注册 (估计的)
50
阶段
- 不适用
联系人和位置
本节提供了进行研究的人员的详细联系信息，以及有关进行该研究的地点的信息。
学习地点
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Ankara、土耳其（türkiye）、06560
- 招聘中
- Gazi Mustafa Kemal Occupational and Environmental Diseases Hospital
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接触：
- Nuriye Kayalı Şendur
- 电话号码：+90 312 212 66 66
- 邮箱：ankaradhs7@saglik.gov.tr
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参与标准
研究人员寻找符合特定描述的人，称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 成人
接受健康志愿者
不
描述
Inclusion Criteria:
- Volunteering to participate in the study
- Being between 18 and 55 years of age
- Being diagnosed with migraine by a neurologist according to the International Classification of Headache Disorders 3 (ICHD-3) criteria
Exclusion Criteria:
- Diagnosis of other primary and/or secondary headaches in addition to migraine,
- Coexisting neurological and/or rheumatological diseases,
- Severe psychiatric disorders (bipolar disorder, schizophrenia, psychosis, etc.),
- Pregnancy or lactation,
- Malignancy,
- Known arrhythmia or presence of any implanted electronic device,
- Presence of sensory loss in the application area,
- Having received physiotherapy or any other treatment in the head/neck region within the last 12 months,
- History of head/neck trauma or surgery within the last 12 months.
学习计划
本节提供研究计划的详细信息，包括研究的设计方式和研究的衡量标准。
研究是如何设计的？
设计细节
- 主要用途：治疗
- 分配：随机化
- 介入模型：并行分配
- 屏蔽：无（打开标签）
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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无干预：Control Group
The control group will receive no intervention and will continue with their routine treatment.
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实验性的：Treatment Group
In addition to routine treatments, a physiotherapy program including transcutaneous auricular vagus nerve stimulation and cervical muscle exercises will be implemented.
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A physiotherapy program including taVNS and cervical muscle exercises
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研究衡量的是什么？
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Pain Assessment
大体时间：Baseline, 8th week (after treatment)
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Individuals' pain parameters will be assessed using a pain diary.
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Baseline, 8th week (after treatment)
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Assessment of Functional Status
大体时间：Baseline, 8th week (after treatment)
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The Migraine Disability Assessment Scale will be used to determine the functional status associated with migraine.
This scale aims to evaluate headache-related disability and the functionality of individuals diagnosed with migraine in daily and social activities.
Score ranges are calculated as follows: Grade I: no loss or very little loss (0-5 days); Grade II: mild loss (6-10 days); Grade III: moderate loss (11-20 days); Grade IV: severe loss (21 days or more)
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Baseline, 8th week (after treatment)
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Quality of Life Assessment
大体时间：Baseline, 8th week (after treatment)
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The Migraine-Specific Quality of Life Scale (Version 2.1) will be used to assess quality of life.
The 14-item scale comprises three sections: role-limiting, role-preventing, and emotional function.
Scores for each subsection range from 0 to 100.
Higher scores indicate better health-related quality of life.
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Baseline, 8th week (after treatment)
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Assessment of Psychological State
大体时间：Baseline, 8th week (after treatment)
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The Hospital Anxiety and Depression Scale will be used to assess psychological status.
Of the 14 items comprising the scale, the 7 odd-numbered items assess anxiety disorder, while the 7 even-numbered items assess depression.
The minimum and maximum scores patients can obtain on either subscale are 0 and 21, respectively.
Higher scores indicate higher levels of depression and anxiety.
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Baseline, 8th week (after treatment)
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Sleep Quality Assessment
大体时间：Baseline, 8th week (after treatment)
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The Single-Item Sleep Quality Scale will be used to assess sleep quality.In this scale, participants are asked the question, "How would you rate your sleep quality overall over the past 7 days?"
Responses are obtained using a numerical rating ranging from 0 (Terrible) to 10 (Excellent) .
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Baseline, 8th week (after treatment)
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查，以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (估计的)
2026年8月1日
初级完成 (估计的)
2027年8月1日
研究完成 (估计的)
2027年8月1日
研究注册日期
首次提交
2026年6月13日
首先提交符合 QC 标准的
2026年6月13日
首次发布 (实际的)
2026年6月18日
研究记录更新
最后更新发布 (实际的)
2026年8月27日
上次提交的符合 QC 标准的更新
2026年8月25日
最后验证
2026年8月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索，没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求，请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改，我们的网站上也会自动更新.