Functional Abilities in Rett Syndrome

This study has been completed.
Sponsor:
Collaborator:
University of Sao Paulo
Information provided by:
Faculdades Metropolitanas Unidas
ClinicalTrials.gov Identifier:
NCT00630422
First received: January 17, 2008
Last updated: March 6, 2008
Last verified: January 2008
  Purpose

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).


Condition
Rett Syndrome

Study Type: Observational
Study Design: Observational Model: Ecologic or Community
Time Perspective: Cross-Sectional
Official Title: Functional Abilities in Rett Syndrome

Resource links provided by NLM:


Further study details as provided by Faculdades Metropolitanas Unidas:

Enrollment: 64
Study Start Date: February 2006
Study Completion Date: December 2006
Primary Completion Date: September 2006 (Final data collection date for primary outcome measure)
Groups/Cohorts
64
All Patients

Detailed Description:

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.

  Eligibility

Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population

This study investigated only patients with Rett syndrome that matched the criteria for the classic form of the disease

Criteria

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
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00630422

Locations
Brazil
Faculdades Metropolitanas Unidas
São Paulo, Brazil, 04505-001
Sponsors and Collaborators
Faculdades Metropolitanas Unidas
University of Sao Paulo
Investigators
Principal Investigator: Carlos BM Monteiro, PhD Faculdades Metropolitanas Unidas
  More Information

Additional Information:
No publications provided

Responsible Party: carlos bandeira de mello monteiro, Faculdades Metropolitanas Unidas
ClinicalTrials.gov Identifier: NCT00630422     History of Changes
Other Study ID Numbers: monteiro, monteiro1
Study First Received: January 17, 2008
Last Updated: March 6, 2008
Health Authority: Brazil: National Committee of Ethics in Research

Keywords provided by Faculdades Metropolitanas Unidas:
Rett Syndrome
Selfcare
Mobility limitation
Interpersonal relations
This study avaliated patients with Rett Syndrome

Additional relevant MeSH terms:
Rett Syndrome
Heredodegenerative Disorders, Nervous System
Neurodegenerative Diseases
Nervous System Diseases
Mental Retardation, X-Linked
Intellectual Disability
Neurobehavioral Manifestations
Neurologic Manifestations
Genetic Diseases, X-Linked
Genetic Diseases, Inborn

ClinicalTrials.gov processed this record on August 19, 2014