Comparing Mirror Therapy Rehabilitation Device to Conventional Mirror Therapy
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 24
- 试验地点
- 2
- 主要终点
- Change in Jebsen-Taylor Hand Function Test score
研究概览
简要总结
This is a randomized controlled trial which will compare conventional mirror therapy with mirror therapy using the Miraπ device which physically moves a patient's affected limb.
This study will use two parallel groups: (1) receiving conventional mirror therapy as a part of the standard of care as conducted by the participant's clinical care team and (2) receiving mirror therapy with the Miraπ device as conducted by study personnel with the oversight of the participant's clinical care team.
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
- 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
- •Participants currently accepted and cleared for rehabilitation in the inpatient rehabilitation unit by the rehabilitation medical director.
- •Participants with paralysis or motor function problems of only one hand.
- •Participants need mirror therapy because of their health condition.
- •Participants' rehabilitation physician determined that mirror therapy would be appropriate for standard of care.
- •Participants are able to memorize easy tasks, and able to follow instructions e.g., moving the healthy fingers.
排除标准
- •Participants who are not cleared physically or medically to participate in standard acute inpatient rehabilitation therapies by the rehabilitation medical director
- •Participants who are not able to memorize easy tasks, e.g., moving the healthy fingers.
- •Participants with spasticity of the affected hand (as assed by the occupational therapist)
- •Vulnerable populations
结局指标
主要结局
Change in Jebsen-Taylor Hand Function Test score
时间窗: At baseline and at discharge (approximately 2-3 weeks after baseline)
Percentage score, which determines how well a participant can do motor tasks for range of motion, strength, and tasks of activities of daily life. Participants have up to 120 seconds to complete tasks. Lower scores indicate less impairment.
McGill Pain Questionnaire (MPQ)
时间窗: At baseline and at discharge (approximately 2-3 weeks after baseline)
The MPQ is scored by summing the values of words that best describe a person's pain. The score ranges from 0 (no pain) to 78 (severe pain)
Change in Visual Analog Scale (VAS) to assess Pain
时间窗: At baseline and at discharge (approximately 2-3 weeks after baseline)
The VAS pain scale is a tool for assessing pain intensity. Participants will be asked to mark a point on a 100 mm horizontal line that represents the intensity of their pain. This line has two endpoints: 0: No pain and 100: Worst possible pain imaginable. The distance from the "0" to the mark is measured in millimeters with the resulting number (0-100) being the VAS pain score
次要结局
未报告次要终点