Functional Abilities in Rett Syndrome

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

64 participants

Study Classification

OBSERVATIONAL

Study Start Date

2006-02-28

Study Completion Date

2006-12-31

Brief Summary

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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).

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Detailed Description

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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.

Conditions

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Rett Syndrome

Study Design

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Observational Model Type

ECOLOGIC_OR_COMMUNITY

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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64

All Patients

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Patients with Rett syndrome that matched the criteria for the classic form of the disease

Exclusion Criteria

* Any other disease;
* Rett syndrome associated with other disease
* Rett syndrome that not that matched the criteria for the classic form of the disease

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes