Treatment Efficacy of Tension Type Headache After Application of Sub-occipital Muscle Inhibition Technique Associated With Interferential Electrotherapy
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 29
- 试验地点
- 2
- 主要终点
- Pain
研究概览
简要总结
The main objective of this study is to determine the effects caused in neck movement, neck pain, headache in patients with tension type headache and cervicogenic headache after application of sub-occipital muscle inhibition technique associated with interferential electrotherapy.
详细描述
This study is based on the combined application of sub-occipital muscle inhibition technique associated with interferential electrotherapy improves symptoms in patients with tension type headache and cervicogenic headache.
The purposes of this study are:
- Evaluate the effectiveness of treatment based on the combined application of sub-occipital muscle inhibition technique associated with interferential electrotherapy in patients with tension type headache.
- Evaluate the effects of treatment caused in upper cervical movement.
- Evaluate the effects of treatment caused in neck pain.
- Evaluate the effects of treatment caused in headache.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Investigator, Outcomes Assessor)
盲法说明
Outcome assessor will be blinded to group allocation. Additionally, analysis blinding will be performed to group allocation.
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients diagnosed with tension type headache
- •In prophylactic regimen and with medical control
排除标准
- •Patients with neurological or cognitive impairments that prevent understanding the questionnaires
- •Patients diagnosed with other types of headaches
- •Patients who have not signed the informed consent document
结局指标
主要结局
Pain
时间窗: Pain will be assessed at baseline, before and after each session (twice a week for 4 weeks)
Our primary outcome will consist of changes at each session in self-reported pain, which will be measured with a visual analogic scale (VAS).
Anxiety
时间窗: STAI will be assessed at baseline and after 4 weeks.
Anxiety will be assessed with the State-Trait Anxiety Inventory. This questionnaire is designed for the self-assessment of anxiety (Cronbach's α for this scale ranges from .83 to .92).
次要结局
- Headache Disability(HDI will be assessed at baseline and after 4 weeks.)
- Headache Impact Test(HIT-6 will be assessed at baseline and after 4 weeks.)
- Range of Motion(ROM will be assessed at baseline and after 4 weeks.)
- Neck Disability Index(NDI will be assessed at baseline and after 4 weeks.)
- SF-36 Health Survey(SF-36 will be assessed at baseline and after 4 weeks.)
- Depression(BECK II will be assessed at baseline and after 4 weeks.)
研究者
Raúl Pérez Llanes
Diplomado en Fisioterapia
Universidad Católica San Antonio de Murcia