Neuropsychological and Psychosocial Follow up of Children and Adolescents With Neuromuscular Disease
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Neuromuscular Diseases
- Sponsor
- Universitaire Ziekenhuizen KU Leuven
- Enrollment
- 300
- Locations
- 1
- Primary Endpoint
- Neuropsychological profile (questionnaires, neuropsychological testing) of children with myotonic dystonia type 1
- Status
- Recruiting
- Last Updated
- last year
Overview
Brief Summary
This project is a retrospective and prospective investigation of neuropsychological and psychosocial development of children with a neuromuscular disease.
Detailed Description
This project is a retrospective and prospective investigation of neuropsychological and psychosocial development of children with a neuromuscular disease. Children and adolescents in UZ Leuven will be evaluated according to a psychosocial and neuropsychological protocol including different psychological tests and patient questionaires.
Investigators
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- Not provided
Outcomes
Primary Outcomes
Neuropsychological profile (questionnaires, neuropsychological testing) of children with myotonic dystonia type 1
Time Frame: one year
Compare the outcome of the questionnaires, IQ test and other neuropsychological test to a normal population