Effects of Respiratory Muscle Training in Obese Women
22 lipca 2019 zaktualizowane przez: Eli Maria Pazzianotto Forti, Universidade Metodista de Piracicaba
Effects of Respiratory Muscle Training on Lung Function, Respiratory Muscle Function and Physical Fitness in Obese Women
The objective of this study will be to evaluate the effects of inspiratory muscle training (IMT) on the physical fitness of obese women
It is believed that the application of these exercises helps in the improvement of inspiratory muscle performance, which should improve physical fitness and thus allow a better performance in the activities of daily living.
Przegląd badań
Status
Zakończony
Interwencja / Leczenie
Szczegółowy opis
This is a clinical trial, in which adult obese volunteers aged 20-59 years will be evaluated, which will be randomized into two groups: training group (GT) and control group (CG).
Both groups should meet the following inclusion criteria: Age between 20 and 59 years, BMI> 35 and <55 kg / m², with clinical stability, able to perform the physical tests and acceptance to participate in the study.
Women with reports of decompensated heart disease, chronic obstructive pulmonary disease and asthma will be excluded; musculoskeletal and / or neuromuscular changes, which make it impossible to perform the tests.
The evaluations will occur in two days with at least 48 hours of interval between them, within a period of seven days, before and after the respiratory muscle training of four weeks.
In addition to anamnesis, the initial evaluation will include assessment of pulmonary function (SLF, forced vital capacity (FVC) and maximal voluntary ventilation (VVM)) by spirometry; respiratory muscle evaluation through the measures of Maximum Inspiratory Pressure (PIMax) and maximal sustained inspiratory pressure (PIMaxS); physical fitness assessment through the 6-minute step test (TD6), incremental shuttle walking test (ISWT) and Sentar e Levantar (SL) test, as well as assessment of dyspnea.
For the TMI will be used equipment with pressure threshold pressure.
During the 4-week period, the IMT will be performed 5 days a week and will consist of 2 series with 30 inspirations.
Inspirations will be performed slowly and protracted.
The training load will be 55% of the PIMáx readjusted weekly.
Statistical analysis will be performed using BioEstat version 5.3.
To evaluate the normality of distribution of the data will be used Shapiro-Wilk test.
For the comparison of all variables studied, the Student's t-test or the Mann-Wittney test will be used.
Pre- and post-training parametric results will also be compared statistically using variance analyzes of two variables (group × time) (ANOVA).
Bonferroni tests will be used to examine differences between groups when indicated by ANOVA.
The significance level of 5% will be adopted for all analyzes (P <0.05) where the data will be expressed as mean and standard deviation.
Typ studiów
Interwencyjne
Zapisy (Rzeczywisty)
30
Faza
- Nie dotyczy
Kontakty i lokalizacje
Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.
Lokalizacje studiów
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São Paulo
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Piracicaba, São Paulo, Brazylia, 13400911
- Universidade Metodista de Piracicaba (UNIMEP)
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Kryteria uczestnictwa
Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.
Kryteria kwalifikacji
Wiek uprawniający do nauki
20 lat do 59 lat (Dorosły)
Akceptuje zdrowych ochotników
Tak
Płeć kwalifikująca się do nauki
Kobieta
Opis
Inclusion Criteria:
- BMI> 35 and <55 kg / m²
- with clinical stability
- suitable for physical tests
- acceptance to participate in the study
Exclusion Criteria:
- women with reports of decompensated heart disease
- chronic obstructive pulmonary disease and asthma
- musculoskeletal and / or neuromuscular changes,
- which make it impossible to perform the tests.
Plan studiów
Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Nielosowe
- Model interwencyjny: Przypisanie czynnikowe
- Maskowanie: Brak (otwarta etykieta)
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
|---|---|
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Brak interwencji: Kontrola
Ta grupa nie otrzyma interwencji
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Eksperymentalny: Inspiratory Muscle Training
This group, for inspiratory muscle training, will use the Powerbreathe® K5 device.
This device will be adjusted with a load of 55% of previously assessed MIP.
The volunteer will be instructed to inhale with sufficient force to overcome the resistance of the equipment and subsequently perform a normal expiration.
During the 4-week period of respiratory muscle training volunteers will be instructed to perform 2 sets with 30 inspiratory efforts, 5 days a week.
The training load will be readjusted on the first day of training each week, after a new reassessment of the PIMax in order to guarantee the overload during inspiratory muscle training.
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Powerbreathe® K5
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Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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EVALUATION OF LUNG VOLUMES AND CAPACITIES
Ramy czasowe: before and after the intervention, for 2 days with a 72-hour interval
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Spirometry will be out according to the guidelines of the American Thoracic Society (ATS) and European Respiratory Society (ERS) (2005).
The values extracted will be selected according to Pereira (2002), and the predicted values calculated using the equation proposed by Pereira et al. (1992) for Brazilians.
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before and after the intervention, for 2 days with a 72-hour interval
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Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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EVALUATION OF PHYSICAL ACTIVITY LEVEL
Ramy czasowe: before and after the intervention, for 2 days with a 72-hour interval
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Volunteers will respond to the International Physical Activity Questionnaire, which is an instrument that allows estimating the weekly time spent in physical activity.
The final classification given by the International Physical Activity Questionnaire occurs in five levels of physical activity: Very Active, Active, Irregularly active and Sedentary.
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before and after the intervention, for 2 days with a 72-hour interval
|
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6-MINUTE DEGREE TEST (TD6)
Ramy czasowe: before and after the intervention, for 2 days with a 72-hour interval
|
The TD6 will be used for the evaluation of cardiorespiratory fitness by calculating the maximum oxygen consumption (VO2 max) in an indirect way and the functional capacity of the volunteers.
The TD6 outcome will be the number of volunteer climbs on the rung (PESSOA et al., 2015).
The values reached in the number and the rhythm of ascents in the step will express the functional capacity.
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before and after the intervention, for 2 days with a 72-hour interval
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INCREMENTAL SHUTTLE WALKING TEST (ISWT)
Ramy czasowe: before and after the intervention, for 2 days with a 72-hour interval
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The ISWT will be used to determine the functional capacity of the volunteers by the distance traveled during the test.
It is a walking test, with progressive loading, given by the increase in walking speed required to overcome each stage of the test.
The ISWT will be controlled by specific software, which determines the speed and pace of each stage of the test.
This test will be carried out in a corridor in which 10 meters in length, delimited by cones, at each end, will be demarcated by volunteers, obeying each sound signal programmed by Sing et al. (1992).
The test will be terminated at the signal of inability to continue or non-accompaniment of speeds by the volunteer.
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before and after the intervention, for 2 days with a 72-hour interval
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TEST TO SIT AND LIFT
Ramy czasowe: before and after the intervention, for 2 days with a 72-hour interval
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This test will be used to determine the indirect force in the lower limbs.
To perform this test, a chair with a height of 40 cm will be used, with backrest, in which the volunteer will begin the test in the sitting position, in the middle of the seat, with the spine erect, feet resting on the floor and the arms crossed against the thorax.
At the investigator's signal, the volunteer should stand up, stand fully up, and then return to the seated position.
Volunteers will be encouraged to sit and stand up as often as possible in 30 seconds.
The result will be determined by counting the number of times the volunteer correctly performed the movements of sitting and lifting of the chair without the aid of the movement of the upper limbs
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before and after the intervention, for 2 days with a 72-hour interval
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EVALUATION OF INSPIRATORY MUSCLE STRENGTH
Ramy czasowe: before and after the intervention, for 2 days with a 72-hour interval
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The Maximum Inspiratory Pressure (PIMax) and Maximum Expiratory Pressure (PEMax) measurements will be performed.
The measures of the MIP will aim beyond the evaluation of the strength of the respiratory muscles, establish the initial load of the resistance test of the respiratory muscles as well as the training load.
The measurements of PImax and PEmax, will be evaluated through an analog manovacuometer.
Each participant should perform three to five maximum inspiratory and reproducible inspiratory efforts provided there has been a maximum difference of 10% between them being the highest value considered for statistical analysis.
The time interval between consecutive measurements was 1 minute.
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before and after the intervention, for 2 days with a 72-hour interval
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Współpracownicy i badacze
Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.
Śledczy
- Główny śledczy: Eli M Pazzianoto-Forti, Phd, Universidade Metodista de Piracicaba
Daty zapisu na studia
Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
15 grudnia 2018
Zakończenie podstawowe (Rzeczywisty)
21 maja 2019
Ukończenie studiów (Rzeczywisty)
8 czerwca 2019
Daty rejestracji na studia
Pierwszy przesłany
17 października 2018
Pierwszy przesłany, który spełnia kryteria kontroli jakości
5 grudnia 2018
Pierwszy wysłany (Rzeczywisty)
6 grudnia 2018
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
24 lipca 2019
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
22 lipca 2019
Ostatnia weryfikacja
1 lipca 2019
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- Tamires2018
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
NIE
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Nie
Bada produkt urządzenia regulowany przez amerykańską FDA
Nie
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