Spinal Dysraphism
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Confirmed diagnosis of chronic diseases; patient with spina bifida;Duchenne muscular dystrophy;Charcot Marie Tooth;congenital dystrophy;congenital myopathy;independent walk; use assistive device;use of wheelchair; age between 8 to 16 year old;answer no to all PAR-Q questions; have less than two risk factors for coronary heart disease from the questionnaire;patients who could develop a maximum cardiopulmonary exercise test confirmed by physician;patients able to follow the instructions;patients with voluntary participation in the research
Exclusion criteria
Exclusion criteria: Patients with comorbidities associated with underlying disease that prevent maximum exertion; recent upper limb fracture;history of hydrocephalus that compromises understanding or lead to neuromuscular changes and cause motor incoordination to perform the tests;children and adolescents whose guardians do not agree to sign the Informed Consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find an increase in aerobic fitness, measured by oxygen consumption, and in muscle endurance, measured by time of fatigue test and peak torque using the Linear Mixed Effects Model method and considering significant an alpha lower than 5% in the preintervention, middle of intervention A, end of intervention A and beginning of intervention B, middle of intervention B, and end of intervention. | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to find a maintenance of aerobic fitness, measured by oxygen consumption, and muscle endurance, measured by time of fatigue and peak torque test using the Linear Mixed Effects Model method and considering significant an alpha lower than 5% in 6 months and 1 year after intervention. | — |
Countries
Brazil
Contacts
Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo - FMRP-USP