Effect of Pilates Training Versus High Intensity Interval Training on Cardiorespiratory Fitness in Asthmatic Patients
22 lipca 2026 zaktualizowane przez: Ghidaa Elmahdi Eldomiaty, Horus University
To compare the effect of Pilates Training Versus High Intensity Interval Training on Cardiorespiratory Fitness in Asthmatic Patients.
Przegląd badań
Status
Jeszcze nie rekrutacja
Warunki
Szczegółowy opis
Asthma is a widespread chronic inflammatory disease affecting over 300 million people globally, leading to approximately 461,000 deaths annually.
Exercise, particularly Pilates and high-intensity interval training, is critical for improving cardiorespiratory fitness and can enhance the quality of life for asthma patients, who often face reduced physical fitness and comorbidities like depression.
Pilates improves respiratory control and strengthens respiratory muscles, while high-intensity interval training enhances aerobic and anaerobic capacities, reduces inflammation, and improves maximal oxygen uptake (VO₂ max).
This study aims to establish guidelines comparing the effects of Pilates and high-intensity interval training on cardiorespiratory fitness in asthmatic patients.
Typ studiów
Interwencyjne
Zapisy (Szacowany)
51
Faza
- Nie dotyczy
Kontakty i lokalizacje
Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.
Kontakt w sprawie studiów
- Nazwa: Ghidaa Elmahdi Eldomiaty, Assistant lecturer
- Numer telefonu: +20 10 22143737
- E-mail: gelmahdi@horus.edu.eg
Lokalizacje studiów
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Damietta, Egipt
- out-patient clinic, faculty of physical therapy, Horus university
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Kontakt:
- Ghidaa Elmahdi Eldomiaty, Assistant lecturer
- Numer telefonu: +20 10 22143737
- E-mail: gelmahdi@horus.edu.eg
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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
- Dorosły
Akceptuje zdrowych ochotników
Nie
Opis
Inclusion Criteria:
- 51 patients diagnosed with a clinical diagnosis of asthma and a history of respiratory illness, aged between 30 and 40 years.
- Medically stable and capable of performing physical exercise.
- All participants provided written informed consent before enrollment.
- body mass index 25.0 - 29.9 (overweight)
- Patients with partially controlled asthma according to the Asthma Control Questionnaire (ACQ) from 0 to 1.5.
Exclusion Criteria:
- Participants with musculoskeletal limitations, cardiovascular instability, or any contraindications to exercise were excluded.
- Uncontrolled hypertension.
- Cognitive impaired patients.
- Severe Anemic patients.
- Pregnancy.
- Recent cardiothoracic surgery.
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: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Pojedynczy
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
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Eksperymentalny: Pilates exercises
Patients will receive Pilates exercises administered to Group A include five movements: The Hundred, Single Leg Stretch, Side Kick, Toe Taps, and Leg Pull Front all performed with structured breathing patterns to emphasize respiratory control and core stabilization.
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17 Patients will perform Pilates exercises 40-60 mins, three times per week, over 8weeks. Pilates exercises include five movements: The Hundred, Single Leg Stretch, Side Kick, Toe Taps, and Leg Pull Front, all performed with structured breathing Patterns To Emphasize Respiratory Control And Core Stabilization
Breathing in slowly and deeply through the nose using the diaphragm with a minimum movement of the chest in a supine position with one hand placed on the chest and the other on the belly.
During breathing, practitioners should be careful that chest remains as still as possible and stomach moves against the hand focusing on contracting the diaphragm.
Generally, diaphragmatic breathing practitioners inhale and exhale for approximately six seconds, respectively
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Eksperymentalny: low-volume high-intensity interval training
Patients will receive low-volume high-intensity interval training.
Participants will perform 3-minute High Intensity Interval Training intervals on a treadmill at 85- 90% of heart rate reserve, each followed by 2 minutes of moderate-intensity active recovery at 60% -70% of eart rate reserve.
The total time spent in the exercise session is 25-30 minutes.
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Breathing in slowly and deeply through the nose using the diaphragm with a minimum movement of the chest in a supine position with one hand placed on the chest and the other on the belly.
During breathing, practitioners should be careful that chest remains as still as possible and stomach moves against the hand focusing on contracting the diaphragm.
Generally, diaphragmatic breathing practitioners inhale and exhale for approximately six seconds, respectively
17 patients will engage in low-volume high-intensity interval training complemented by diaphragmatic breathing exercises.
Each session begins with a 5-10 minute warm-up on a treadmill at 40% of heart rate reserve.
The targeted heart rate during high-intensity interval training is set at 85-90% of heart rate reserve plus resting heart rate.
Participants will complete 3-minute high-intensity interval training intervals at the specified intensity, alternating with 2 minutes of moderate-intensity recovery at 60-70% heart rate reserve.
Total exercise duration is 25-30 minutes, concluding with a 5-minute cool-down at 30% heart rate reserve.
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Aktywny komparator: Diaphragmatic breathing exercises
Diaphragmatic breathing exercises involve inhaling slowly through the nose while keeping the chest still and allowing the diaphragm to move the stomach.
This is performed in a supine position, with one hand on the chest and the other on the belly, ensuring minimal chest movement.
Practitioners typically inhale and exhale over six seconds each.
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Breathing in slowly and deeply through the nose using the diaphragm with a minimum movement of the chest in a supine position with one hand placed on the chest and the other on the belly.
During breathing, practitioners should be careful that chest remains as still as possible and stomach moves against the hand focusing on contracting the diaphragm.
Generally, diaphragmatic breathing practitioners inhale and exhale for approximately six seconds, respectively
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Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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assessment of maximum oxygen consumption
Ramy czasowe: At baseline and after 8 weeks
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Cardiopulmonary exercise testing is essential for evaluating patient symptoms, disease severity, prognosis, and therapy responses.
It assesses the interaction of cardiovascular and pulmonary systems with other bodily systems.
maximum oxygen consumption is calculated using the Bruce protocol via the Ergo Spiro Device.
This protocol involves a multi-stage treadmill test, starting at a 10% grade and increasing speed and grade every three minutes until exhaustion.
Subjects must refrain from eating, smoking, and consuming caffeine before testing, and avoid intense exercise leading up to the test.
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At baseline and after 8 weeks
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Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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assessment of Quality of Life
Ramy czasowe: At baseline and after 8 weeks
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The Mini-Asthma Quality of Life Questionnaire is a shortened, 15-item version of the original questionnaire, designed to accurately assess the quality of life in asthmatic patients without consuming much time.
It evaluates four domains: symptoms, activity limitation, emotional function, and environmental stimuli, based on the respondents' experiences over the past two weeks.
it employs a 7-point Likert scale, where 7 indicates no impairment and 1 signifies significant impairment
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At baseline and after 8 weeks
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assessment of dyspnea
Ramy czasowe: At baseline and after 8 weeks
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The Modified Borg Dyspnea Scale is a validated, numerical rating scale used to quantify the subjective perception of breathlessness during physical activity or exercise.
The scale ranges from 0 to 10, where 0 indicates no breathlessness and 10 represents maximal or extremely severe breathlessness.
Participants are instructed to rate their perceived level of dyspnea immediately after or during exercise, providing a simple, reliable, and clinically applicable measure of symptom intensity for monitoring exercise tolerance and evaluating treatment outcomes.
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At baseline and after 8 weeks
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assessment of asthma symptoms
Ramy czasowe: At baseline and after 8 weeks
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Asthma Control Questionnaire (ACQ-6) is a six-item questionnaire designed to measure asthma symptoms.
The questionnaire is scored by the mean of all items (0-6), with higher scores indicating poorer control.
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At baseline and after 8 weeks
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Współpracownicy i badacze
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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 (Szacowany)
25 lipca 2026
Zakończenie podstawowe (Szacowany)
1 listopada 2026
Ukończenie studiów (Szacowany)
30 listopada 2026
Daty rejestracji na studia
Pierwszy przesłany
22 lipca 2026
Pierwszy przesłany, który spełnia kryteria kontroli jakości
22 lipca 2026
Pierwszy wysłany (Rzeczywisty)
27 lipca 2026
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
27 lipca 2026
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
22 lipca 2026
Ostatnia weryfikacja
1 lipca 2026
Więcej informacji
Terminy związane z tym badaniem
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- Ghidaa-PHD
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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