NCT00649753已完成不适用
An Investigation of Algometer Readings for DeJarnette Category II Indicators After Category II Blocking and Cranial Protocol
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 40
- 试验地点
- 2
- 主要终点
- Algometer readings
研究概览
简要总结
The purpose of this study is to evaluate the relationship of pelvic blocking and protocol for cranial adjusting with specific pain areas as outlined by Dr. Bertrand DeJarnette in the Category II/sacroiliac protocol. An algometer will be used to determine the level of pain at specific points before and after each treatment of pelvic blocking with or without cranial adjusting.
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
- Single (Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 60 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Logan student, staff or faculty
- •Age 18 - 60
- •No chiropractic adjustment 2 weeks prior to beginning the study
- •Show the DeJarnette Category II indicators
排除标准
- •Previous lower extremity, first rib and spine injury, surgery
- •Local infection, injury or other malignancy affecting the lower extremity and the nervous system
- •Unstable joints of the lower extremity and/or first rib and/or spine
- •Prescription or herbal muscle stimulants, relaxants, etc. that could affect the nervous system
- •Contraindication to DeJarnette Category II Pelvis Blocking
- •Pregnancy
- •Significant lower lumbar involvement
- •Diabetes, shortness of breath on light physical activity, cardiovascular disease
- •Numbness and/or tingling in the lower extremities
结局指标
主要结局
Algometer readings
时间窗: pre and post treatment intervention
次要结局
未报告次要终点
研究者
研究点 (2)
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