NCT00630422已完成不适用
Functional Abilities in Rett Syndrome
Faculdades Metropolitanas Unidas1 个研究点 分布在 1 个国家目标入组 64 人开始时间: 2006年2月最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 64
- 试验地点
- 1
研究概览
简要总结
The purpose of this study is to evaluate and determinate the functional abilities in Rett syndrome conforming to the established Pediatric Evaluation of Disability Inventory (PEDI).
详细描述
Rett syndrome (RS) is a progressive neurological disturbance of genetic cause that affects females almost exclusively. It is caused by mutations, usually sporadic, of the MECP2 gene located in the X chromosome. In consequence to the serious cognitive and motor compromise, the RS patients have great difficulty in accomplishing day-to-day tasks. The objective of this work is to evaluate the functional abilities in RS to help therapists in theirs treatments programs.
研究设计
- 研究类型
- Observational
- 观察模型
- Ecologic Or Community
- 时间视角
- Cross Sectional
入排标准
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Patients with Rett syndrome that matched the criteria for the classic form of the disease
排除标准
- •Any other disease;
- •Rett syndrome associated with other disease
- •Rett syndrome that not that matched the criteria for the classic form of the disease
研究者
研究点 (1)
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