Asthma
Conditions
Interventions
In this study, 3 groups will be formed, with 20 participants each group, a total of 60 individuals. The control group (CG), composed of participants who will perform two evaluations, the second evalua
the Pilates Group (GP) will undergo Pilates sessions with the traditional breathing of the
technique for 2 months and 2 weeks, with two weekly sessions of 60 minutes. Pilates will perform as many exer
Other
E02.779.474
E02.190.525.186
Sponsors
Universidade Federal de Pernambuco
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
Eligibility
Sex/Gender
Female
Age
7 Years to 15 Years
Inclusion criteria
Inclusion criteria: Patients of both sexes; Age from 7 to 15 years; Pacients with persistent asthma moderate and severe; In outpatient follow-up regular.
Exclusion criteria
Exclusion criteria: Volunteers who had episodes of recent respiratory infections (less than 30 days); Cardiovascular, orthopedic and rheumatologic diseases; Non-performance of lung function tests; Absences from sessions (25% or more).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Expected outcome 1 will be the improvement of disease control through the infant asthma control test for children under 12 years C-ACT and ACT for children over 12 years of age comparing the initial and final outcome.;Expected outcome 2 will be the improvement of quality of life through the PAQLQ instrument analyzing the value before and after the intervention.;Expected outcome 3 will be the improvement of sleep quality analyzed before and after the intervention by the Sleep Behavior Questionnaire, for the parents or guardians of children from 7 to 14 years of age and the Pittsburgh Sleep Quality Index (PQSI) for children and adolescentes. ;Expected outcome 4 will be the difference of the values of the manuvacuometry in the initial and final evaluation, which includes the measures of the maximum inspiratory pressure and maximum expiratory pressure. | — |
Secondary
| Measure | Time frame |
|---|---|
| Expected outcome 1 will be spirometry, analyzing the measurements of FVC, FEV1, FEF 25 and 75% and the FVC / FEV1 ratio, pre and post intervention. ;Expected outcome 2 will be the evaluation by IOS, evaluating the following parameters: R5, R20, R5-R20 and X5, comparing the result of the initial and final evaluation. ;Expected outcome 3 will be the physical tolerance for the 3min Step test; including measures of vital signs: SpO2, Pa, Fc, Fr and Borg scale, analyzing the initial and final evaluation. | — |
Countries
Brazil
Contacts
Public ContactCaroline Franco
Universidade Federal de Pernambuco
Outcome results
None listed