NCT00624988Unknown1 期
The Effect of Vibration Therapy on the Bone Density of the Tiba in Patients With Spinal Cord Injury
适应症
干预措施
试验速览
- 阶段
- 1 期
- 入组人数
- 10
- 试验地点
- 2
- 主要终点
- Bone density scan
研究概览
简要总结
The purpose of this investigation is to determine the effect of lower limb vibration therapy on bone density in the tibia in patients with spinal cord injury. The second purpose is to assess the neuromuscular junction variability at the motor units of the tibialis anterior muscle after a sequence of lower limb vibration therapy
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 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Over the age of 18 years
- •A spinal cord injury patient with injury above T12
- •Injury below T4 to avoid respiratory complication.
- •An ASIA classification of A or B
排除标准
- •Non complicating organic factors such as heart disease, high blood pressure, stroke
- •Exercise where electrical therapy is used while the trial is being conducted
- •A bone density measure 3 times below normal mineralization levels as measured on the first bone density scan prior to entry in to the study
- •Surgical implants below the level of T12
- •Local infection, acute inflammation, injury, tumors or other malignancy, recent wounds, diabetes
- •Any unstable joints of the lower extremity, recent hip and knee joints or fitted hip or knee pins, bolts and/or plates
- •Acute thrombosis
- •Severe migraine, epilepsy
- •Serious cardiovascular disease, wearing a pacemaker
- •Any Spinal manipulation within one year of the study
- •Any implanted device or prosthesis or intrauterine IUD type of device pregnancy
研究组 & 干预措施
Vibration Therapy
Experimental
Treatment will consist of 10 sessions of 60 seconds each with one minute intervals in between at 50 Hz frequency three times per week for three months.
干预措施: Vibration Therapy (Procedure)
结局指标
主要结局
Bone density scan
时间窗: within 7 days pre/post intervention
次要结局
- Single fiber EMG at neuromuscular junction(7 days pre/post intervention)
研究者
研究点 (2)
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