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针对原发性头痛(偏头痛和/或丛集性头痛)的瑜伽式动作研究 - YOURHEAD - 一项试点研究

2026年9月18日 更新者:Marian Papp、Karolinska Institutet

瑜伽基础练习作为偏头痛和/或丛集性头痛的补充治疗 YOURHEAD - 一项试点研究

Migraine and/or Cluster Headache: Study Overview

**Background:** Migraine and cluster headache are two primary headache disorders that significantly impact quality of life and functionality in those affected. According to the WHO's recurring burden of disease reports, migraine is among the neurological conditions responsible for the highest number of years lost due to illness. The headaches associated with migraine and cluster headache range from moderate to severe and cause great suffering. Available treatments do not work for everyone and are often associated with adverse side effects. Physical activity has been shown in several studies to have a positive effect on headache. Given the high prevalence of mental health issues, stress, and sleep problems within this patient group, relaxation and low-intensity exercise such as yoga-based movements (YB) could potentially help individuals improve sleep and well-being, while also providing some preventive effect on headaches.

**Hypothesis:**

Individuals with severe migraine or cluster headache have a strong need for new treatment options. Alternative therapies such as yoga-based exercises, when combined with standard medical treatment as per clinical guidelines, may positively impact:

  1. Headache symptoms and frequency
  2. Sleep quality
  3. Overall life quality

**Purpose and Goals:** This pilot study aims to evaluate the feasibiiity of a web-based yoga or live face to face (FTF) intervention in individuals suffering from severe primary headaches-mainly chronic migraine and/or cluster headache. The study will assess the effect of YB on health-related quality of life, with a focus on sleep quality and mental health as depression and anxiety. A secondary objective is to analyze changes in headache frequency, intensity, and duration associated with primary headache conditions. The pilot study will follow later on with a RCT study (will be registered later). The RCT study will have a comparison group to conventional treatment.

**Relevance for the Patient Group:** The core objective of the project is to determine whether yoga-based exercises can serve as a complementary treatment to enhance quality of life and health in patients with severe primary headache. To ensure equal healthcare access, this intervention will be delivered in digital format and/or FTF to optimize availability and expand care for individuals with primary headache disorders. These efforts aim to improve life quality and well-being in a vulnerable patient population. Headache conditions often affect individuals in their most productive years, and many live with symptoms for decades. Both work and private life are frequently disrupted, resulting in sick leave and social isolation. Close relatives are also affected, as those suffering from headaches require more recovery time to cope with daily life. With this proposed project, we aim to use physical yoga, rooted in holistic traditional medicine, to help individuals with severe primary headache achieve better physical and mental health-particularly improved sleep quality, which in turn enhances overall life quality.

研究概览

详细说明

Current Situation

Migraine and cluster headache are two neurological conditions characterized by recurrent attacks of severe headache. Approximately 14% of the population is estimated to suffer from migraines, while cluster headaches have a prevalence of around 0.1%. The phenotype is marked by unilateral headache attacks lasting approximately 15 minutes to three hours for cluster headache and three hours to three days for migraine. Acute treatment for migraines and cluster headaches typically involves triptans or oxygen therapy to break the attacks, and prophylactic treatment when needed.

Studies have shown that individuals with headaches experience significant impacts on quality of life and often suffer from mental health issues. Research from Karolinska Institutet and the Headache Centre in Copenhagen has demonstrated sleep disturbances among individuals with cluster headaches. Sleep-related diagnoses are also frequently reported in individuals with migraine, and migraine is more prevalent among shift workers compared to non-shift workers. Collectively, these studies indicate a strong connection between sleep problems, mental health, and headache.

The disease burden in high-frequency migraine, chronic migraine, and cluster headache is substantial, and additional alternative treatments are needed alongside standard pharmaceutical therapies. Individuals with these headache types report higher sick leave rates than the general population, and cluster headache sufferers with concurrent mental health issues show increased prevalence for long-term sick leave and disability pension.

Role of Yoga-Based Exercises (YB)

Yoga-based exercises have gained attention in healthcare and are used as complementary treatments for various conditions. Reviews and meta-analyses show effects on stress symptoms, mental states such as sleep disturbances and depression. Web-based yoga interventions have also improved sleep and stress, as well as chronic neck and back pain. Improvements have been observed in endothelial function and inflammation markers.

A review article from China indicates that physical yoga (similar to the planned intervention) appears to reduce headache intensity, duration, and frequency. Previous studies show reductions in migraine headache following yoga interventions, and smaller Indian studies report effects on headache intensity and quality of life in migraine. Research in Western contexts is limited and studies conducted in India tend to show more positive results-possibly due to higher treatment dosages or contextual influences, including placebo or Hawthorne effects.

The American Migraine Foundation recommends yoga-based exercises as a complementary treatment for stress reduction and migraine symptom management, as stress is a common migraine trigger. There is currently no research on yoga-based interventions for cluster headaches, and only a few published studies on migraines.

Traditional Medical Practices

Indian traditional medicine recommends specific exercises (e.g., inversions) for treating headaches, high blood pressure, and improving sleep quality and insomnia. Inversions appear to activate deep brain regions related to sleep and have a calming effect. Sleep disorders often trigger migraines and vice versa. Melatonin rhythms, which may be unstable in headache conditions, often stabilize following yoga-based interventions.

研究类型

介入性

注册 (估计的)

20

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

      • Huddinge、瑞典、141 83
        • Karolinska Institutet

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

18年 至 65年 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Diagnosed chronic migraine and/or cluster (Hortons) headache
  • Men and women 18-65 years
  • Diagnosed with chronic/high frequency migraine (≥15 headache days/month with at least ≥8 with migraine)
  • Diagnosed with chronic cluster head ache (i.e shorter remission than 3 months per year), diagnosed according to ICHD-III criteria.
  • Ability to perform yoga based moments and to give consent.
  • Internet connection with computer/ipad/mobile to perform digitally/tele-health instructions

Exclusion Criteria:

  • Recent or planned operations during the last 6 weeks
  • Drug dependence, alcohol dependence, mental disorders as psychosis, bipolar disorder, anxiety as PTSD etc)
  • Parallel enrollment in other clinical trails
  • Unmedicated high blood pressure, heart disease as heart failure
  • Non Swedish speaking
  • Not able to perform low intensity exercise at home or FTF (face to face) - both online or live.
  • Participants unsure to participate due to drug addiction or other causes
  • Disorientation and not able to inform regarding other serious conditions

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:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Intervention

Yogabased movements weekly (online live or face to face) for primary headaches

Yogabased movements weekly (online) or face to face for primary headaches"

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
Headache diary - frequency, intensity and duration
大体时间:Baseline and after the 8-12 weeks after the intervention and follow-up after 3 and 6 months

Headache frequency (number of days a month and number of attacks per day), headache intensity/pain using a VAS-scale, head ache duration (number of hours/minutes during an attack).

Baseline and after the 8-12 weeks after the intervention and follow-up after 3 and 6 months

次要结果测量

结果测量
措施说明
大体时间
Hospital Anxiety and Depression Scale (HADS)
大体时间:Baseline and after intervention of 8-12 weeks and follow-up after 3 and 6 months

HADS Hospital Anxiety and Depression Scale (HADS) is a self-report questionnaire designed to assess anxiety and depression levels in individuals, particularly in non-psychiatric hospital settings. Structure: The questionnaire consists of 14 items, divided into two subscales: HADS-A for anxiety and HADS-D for depression. HADS uses a 4-point Likert scale (0 = not at all, 3 = most of the time), with separate scores for anxiety and depression subscales (0-21 each). Total scores range from 0 to 42, with higher scores indicating greater symptom severity. Cut-off scores for interpretation include:

0-7: Normal. 8-10: Mild. 11-21: Moderate to severe.

Baseline and after intervention of 8-12 weeks and follow-up after 3 and 6 months
Dysfunctional Beliefs and attitudes about sleep (DBAS-10)
大体时间:Baseline and after 8-12 weeks of intervention and follow-up after 3 and 6 months

Measures sleep related cognitions in a VAS-scale. The scale identifies specific, irrationell and affective thoughts that can disturb insomnia and evaluated sleep related cognitions. Factor I (5 items) was labeled Beliefs about the Immediate Negative Consequences of Insomnia. Factor II (3 items) was labeled Beliefs about the Long-term Negative Consequences on Insomnia. Factor III was labeled Beliefs about the Need for Control Over Insomnia (2 items). Administration time 10 minutes

Baseline and after 8-12 weeks of intervention and follow-up after 3 and 6 months
Karolinska Sleep questionnarie (KSQ) - subjective sleepiness
大体时间:Baseline and 8-12 after the intervention as well as follow-up 3 months and 6 months

KSQ includes 18 questions - on a 6 graded likert scale between 0-5, where 0 = never and 5 = always. It is also possible to calculate index-values.

There are cut-off values to compare with a healthy population or other studies with the same disorder. There are cut-offs for KSQ for normal swedish population but also using the 90:e percentile for a swedish population (different for men and women)

Baseline and 8-12 after the intervention as well as follow-up 3 months and 6 months
Sleep quality using insomnia severity scale (ISI)
大体时间:Baseline and 8-12 weeks after the intervention, follow up after 3 and 6 months

Total score from 0-28 - a score of 0-7 no clinical insomnia, 8-14 no insomnia, 15-21 clinical insomnia moderate, 22-28 clinical insomnia severe

Baseline and 8-12 weeks after the intervention, follow up after 3 and 6 months
Perceived stress scale (PSS-10)
大体时间:Baseline and after 8-12 week intervention, follow-up after 3 and 6 months

The interpretation of PSS-10 scores is not diagnostic but provides a general sense of where a person falls on the spectrum of perceived stress. Generally, a score between 0-13 is considered low stress, 14-26 is moderate stress, and 27-40 is high stress.

Baseline and after 8-12 week intervention, follow-up after 3 and 6 months
Generalized Anxiety Disorder scale (GAD-7)
大体时间:Baseline and 8-12 after the intervention as well as follow-up 3 months and 6 months

The GAD-7 score helps assess the severity of anxiety symptoms, with scores ranging from 0 to 21 indicating varying levels of anxiety severity.

0 - 4: No to Minimal Symptoms - Indicates little to no anxiety symptoms. 5 - 9: Mild Symptoms - Suggests mild anxiety that may not significantly impact daily functioning.

10 - 14: Moderate Symptoms - Indicates moderate anxiety, which may affect daily activities and quality of life.

15 - 21: Severe Symptoms - Reflects severe anxiety that likely requires clinical intervention and support.

Clinical Relevance A score of 10 or higher may indicate a preliminary diagnosis of Generalized Anxiety Disorder (GAD).

Baseline and 8-12 after the intervention as well as follow-up 3 months and 6 months
Nijmegen Dysfunctional breathing scale
大体时间:Baseline and after 8-12 weeks after the intervention and 3 and 6 months follow-up

The Nijmegen Questionnaire (often called the Nijmegen Dysfunctional Breathing Scale) is a validated screening tool designed to identify symptoms of dysfunctional breathing, particularly hyperventilation syndrome. It consists of 16 symptom items scored on a 0-4 scale, with higher scores indicating greater respiratory distress. A total score above 19-23 suggests clinically relevant breathing dysfunction. 16 items covering common symptoms such as chest pain, dizziness, blurred vision, shortness of breath, and feelings of tension.

Each item is rated on a 5-point Likert scale: 0 = Never, 1 = Rarely, 2 = Sometimes, 3 = Often, 4 = Very often.

  • 19 points: Indicates possible dysfunctional breathing or hyperventilation.
  • 23 points: Stronger indication of hyperventilation syndrome
Baseline and after 8-12 weeks after the intervention and 3 and 6 months follow-up
Migraine Disability Assessment Test (MIDAS)
大体时间:Baseline and after 8-12 weeks after the intervention and 3 and 6 months follow-up

MIDAS measures the impact on headaches on quality of life. The patients fills in the total days with headache of different activites. Includes 5 questions, low score indicates little or no disability (0-5) grade 1, 4 different grades, score 6-10 is mild disability grade 2, while 11-20 is moderate disabilty and grade 3, 21+ score indicates severy disability and is grade 4. Points above 6 requires consultation with doctor

Baseline and after 8-12 weeks after the intervention and 3 and 6 months follow-up

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 (实际的)

2026年1月1日

初级完成 (估计的)

2026年12月1日

研究完成 (估计的)

2026年12月30日

研究注册日期

首次提交

2025年12月5日

首先提交符合 QC 标准的

2025年12月5日

首次发布 (实际的)

2025年12月18日

研究记录更新

最后更新发布 (实际的)

2026年9月23日

上次提交的符合 QC 标准的更新

2026年9月18日

最后验证

2026年7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.

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