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Clinical Trials/NCT05825638
NCT05825638CompletedNot Applicable

Evolution of Pulsed Oxygen Saturation Throughout an Interval Training Session Compared to a Continuous Training Session in Patients With Chronic Obstructive Pulmonary Disease With Exercise-induced Oxygen Desaturation.

Groupe Hospitalier du Havre1 site in 1 country12 target enrollmentStarted: January 10, 2023Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
12
Locations
1
Primary Endpoint
Difference in oxygen pulsed saturation

Study Overview

Brief Summary

A problem often observed during exercise training is oxygen desaturation exclusively during exercise in some patients. In the case of exercise-induced desaturation, it may be suggested to train these patients in interval training to limit exercise-induced desaturation. Interval training consists of alternating active phases of short duration (often 30 seconds to 1 minute) followed by a short active or passive recovery phase of equivalent duration to the previous phase. Investigators therefore hypothesise that interval training on a cycloergometer or treadmill can limit exercise-induced desaturation in COPD patients.

The aim of the study is to observe the evolution of pulsed oxygen saturation between a continuous training session and a interval training session.

Study Design

Study Type
Observational
Observational Model
Case Crossover
Time Perspective
Prospective

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • a diagnosis of COPD
  • participating in a pulmonary rehabilitation programme
  • with an exercise-induced desaturation less than 90%
  • no oxygen supplementation

Exclusion Criteria

  • Under 18 years of age
  • 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

Outcomes

Primary Outcomes

Difference in oxygen pulsed saturation

Time Frame: One week

Difference in minimum saturation during both exercise, the measurement will be performed with a pulse oximeter (Spirodoc, MIR)

Secondary Outcomes

  • Difference in oxygen pulsed saturation(One week)
  • Difference in respiratory rate(One week)
  • Difference in tidal volume(One week)
  • Difference in peripheral muscle oxygenation(One week)
  • Difference in inspiratory capacity(One week)
  • Difference in muscle discomfort(One week)
  • Difference in Dyspnea(One week)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Guillaume Prieur

Principal Investigator

Groupe Hospitalier du Havre

Study Sites (1)

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