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临床试验/NCT03862638
NCT03862638已完成不适用

Yoga Therapy for Chronic Tension-Type Headache: An Evaluation Study

NMP Medical Research Institute2 个研究点 分布在 1 个国家目标入组 68 人开始时间: 2010年4月10日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
68
试验地点
2
主要终点
The number of days with headache

研究概览

简要总结

Chronic tension headache represents a considerable social burden in terms of both costs to the health services and also the costs of lost productivity. Episodic tension-type headache can be treated with rest and analgesics, while chronic tension-type headache demands a more fundamental treatment.

Effectiveness of yoga therapy in the management of chronic tension type headache is limited. In this study, yoga therapy was used to explore its effect on chronic tension-type headache.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Meeting the diagnostic criteria of CTTH in the international classification of headache disorders, 3rd edition (beta version) (ICHD-III beta);
  • Aged 18-55 years;
  • Having the ability of understanding and completing the headache dairy;
  • Provide written informed consent.

排除标准

  • No headache during the pervious 3 months;
  • Taking any prophylactic medication during the previous one month;
  • Secondary headache or any systematic cause
  • Having serious conditions of the heart, liver, kidney or other organs;
  • In pregnancy or lactation, or planning to be pregnant in 6 months;
  • Drug and Substance abuse
  • Diagnosed psychiatric condition
  • Taking any other complementary and alternative medicines
  • Practicing yoga of any kind in last three months

结局指标

主要结局

The number of days with headache

时间窗: Change from baseline to 12-week of intervention

Number of days with headache every four weeks were assessed through headache diaries

次要结局

  • The medication intake(Change from baseline to 12 week of intervention)
  • Intensity of Pan(Change from baseline to12 week of intervention)
  • Duration of Pain(Change from baseline to12 week of intervention)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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