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AsthmaNCT07728578

Effect of Pilates Training Versus High Intensity Interval Training on Cardiorespiratory Fitness in Asthmatic Patients

A study testing Pilates exercises, low-volume high-intensity interval training and diaphragmatic breathing exercise. in people with Asthma, run by Horus University at 1 site in Egypt.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

To compare the effect of Pilates Training Versus High Intensity Interval Training on Cardiorespiratory Fitness in Asthmatic Patients. Read more about this study

Who is it for?
Ages 30 to 40 years
Conditions the study is for
Asthma
What is being tested?
Pilates exercises, low-volume high-intensity interval training and diaphragmatic breathing exercise.
Could I receive a placebo?
No, everyone receives an active treatment
How many people
51 participants
Where
1 siteEgypt
Study dates
25 Jul 2026to 30 Nov 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 30 to 40 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • 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.

Who cannot join

  • 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.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Ghidaa Elmahdi Eldomiaty, Assistant lecturer contact

+20 10 22143737

gelmahdi@horus.edu.eg

Egypt1 site
  • out-patient clinic, faculty of physical therapy, Horus university

    Damietta

    Ghidaa Elmahdi Eldomiaty, Assistant lecturer, +20 10 22143737, gelmahdi@horus.edu.eg

Other trials in Egypt

About this study

To compare the effect of Pilates Training Versus High Intensity Interval Training on Cardiorespiratory Fitness in Asthmatic Patients.

Read the detailed description

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.

Conditions
Asthma
Being tested
Pilates exercises, low-volume high-intensity interval training, diaphragmatic breathing exercise.
Medical subject headings
Asthma

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Pilates exercisesOther

    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

  • low-volume high-intensity interval trainingOther

    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.

  • diaphragmatic breathing exercise.Other

    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

Study groups in NCT07728578
Study groupRoleWhat they receive
Pilates exercisesExperimentalPatients 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.
Receives: Other: Pilates exercises; Other: diaphragmatic breathing exercise.
low-volume high-intensity interval trainingExperimentalPatients 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.
Receives: Other: low-volume high-intensity interval training; Other: diaphragmatic breathing exercise.
Diaphragmatic breathing exercisesActive comparatorDiaphragmatic 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.
Receives: Other: diaphragmatic breathing exercise.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. assessment of maximum oxygen consumption

    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.

    Measured: At baseline and after 8 weeks

Secondary outcomes (3)
  1. assessment of Quality of Life

    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

    Measured: At baseline and after 8 weeks

  2. assessment of dyspnea

    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.

    Measured: At baseline and after 8 weeks

  3. assessment of asthma symptoms

    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.

    Measured: At baseline and after 8 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 Jul 2026
  2. Study start25 Jul 2026 (estimated)
  3. Primary completion1 Nov 2026 (estimated)
  4. Study completion30 Nov 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
51 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07728578
Sponsor's protocol ID
Ghidaa-PHD
Status last verified
Jul 2026
First submitted
22 Jul 2026
Last updated
27 Jul 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Pilates exercises, low-volume high-intensity interval training and diaphragmatic breathing exercise. in people with Asthma, run by Horus University at 1 site in Egypt.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 27 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Ghidaa Elmahdi Eldomiaty, Assistant lecturer (+20 10 22143737, gelmahdi@horus.edu.eg), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

assessment of maximum oxygen consumption (time frame: At baseline and after 8 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 Jul 2026.

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