The practice of Pilates exercises associated with Buteyko exercises in children and adolescents with asthma

Not Applicable

Recruiting

• Conditions: Asthma; C08.127.108

• Registration Number: RBR-5hq3xh
• Lead Sponsor: niversidade Federal de Pernambuco

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2018-07-25
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: Not specified

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

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).

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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 Outcome Measures

Name	Time	Method
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.<br>;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.<br>;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.