Evolution of Pulsed Oxygen Saturation During Interval Training Compared to Continuous Training in COPD Patients
NCT ID: NCT05825638
Last Updated: 2026-01-21
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
12 participants
OBSERVATIONAL
2023-01-10
2025-10-10
Brief Summary
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The aim of the study is to observe the evolution of pulsed oxygen saturation between a continuous training session and a interval training session.
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Detailed Description
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Conditions
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Study Design
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CASE_CROSSOVER
PROSPECTIVE
Study Groups
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Continuous training session
Continuous training session
Continuous training consists of a 5 minute warm up, 5 minute cool down and 20 minutes of moderate intensity work. The workload is set at 60% of the patient's maximum power
Interval Training session
Interval training session
Interval training consists of a 5-minute warm-up, a 5-minute cool-down and 20 minutes of alternating 60 seconds of high-intensity work (100% of the maximum power recorded in the incremental test that was carried out when the patient was admitted to the pulmonary rehabilitation department) and 60 seconds of unloaded pedalling or rest.
Interventions
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Continuous training session
Continuous training consists of a 5 minute warm up, 5 minute cool down and 20 minutes of moderate intensity work. The workload is set at 60% of the patient's maximum power
Interval training session
Interval training consists of a 5-minute warm-up, a 5-minute cool-down and 20 minutes of alternating 60 seconds of high-intensity work (100% of the maximum power recorded in the incremental test that was carried out when the patient was admitted to the pulmonary rehabilitation department) and 60 seconds of unloaded pedalling or rest.
Eligibility Criteria
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Inclusion Criteria
* participating in a pulmonary rehabilitation programme
* with an exercise-induced desaturation less than 90%
* no oxygen supplementation
Exclusion Criteria
* Pregnant woman
* Person not affiliated to a health insurance regime or not benefiting from a social security regime
* Patient under curatorship, guardianship or safeguard of justice
* Patient speaking a language other than French
* Patient with severe hypoxaemia (SpO2 ≤ 80%) during exercise
* Patient having had a moderate or severe exacerbation (hospitalisation for respiratory reasons) in the previous 4 weeks
* Patients with orthopaedic, rheumatic, vascular or neurological pathology limiting their ability to make an effort
* Breastfeeding women
ALL
No
Sponsors
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Medrinal Clement
UNKNOWN
Combret Yann
UNKNOWN
Machefert Margaux
UNKNOWN
Groupe Hospitalier du Havre
OTHER
Responsible Party
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Guillaume Prieur
Principal Investigator
Principal Investigators
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Guillaume Prieur, PT, PhD
Role: PRINCIPAL_INVESTIGATOR
Groupe Hospitalier du Havre
Locations
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Groupe Hospitalier du Havre
Le Havre, Normandy, France
Countries
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Other Identifiers
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2022-A02087-36
Identifier Type: -
Identifier Source: org_study_id
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