NCT07707271 Continuous Versus High Intensity Interval Exercise in Chronic Obstructive Pulmonary Disease
| NCT ID | NCT07707271 |
| Status | Recruiting |
| Phase | — |
| Sponsor | George Papanicolaou Hospital |
| Condition | COPD |
| Study Type | INTERVENTIONAL |
| Enrollment | 12 participants |
| Start Date | 2026-06 |
| Primary Completion | 2027-06 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 12 participants in total. It began in 2026-06 with a primary completion date of 2027-06.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
Chronic Obstructive Pulmonary Disease (COPD) is characterized by exercise intolerance, which is a prognostic factor of disease severity and mortality and is usually attributed to ventilatory limitations. Emerging evidence indicates that cerebral oxygenation may also be an important contributor, being impaired both at rest and during exercise in COPD patients. Furthermore, abnormal systemic hemodynamic responses and autonomic nervous system (ANS) dysfunction have been observed, which may further impair cerebral oxygenation. The type of exercise training applied in pulmonary rehabilitation (continuous versus interval) appears to influence these mechanisms differently, yet evidence on their impact on cerebral oxygenation in COPD remains scarce. The aim of this study is to compare, for the first time, the acute changes in cerebral oxygenation, CPET parameters, systemic hemodynamic responses, and autonomic responses in patients with COPD who undergo a high-intensity interval aerobic exercise (HIIE) protocol versus a moderate-intensity continuous aerobic exercise (MICE) protocol. These findings will have important clinical implications, as they may guide the choice of the most appropriate exercise modality in pulmonary rehabilitation.
Eligibility Criteria
Inclusion Criteria: * Clinical diagnosis of COPD based on smoking history (pack/years) or exposure to other risk factors and post bronchodilation forced expiratory volume (FEV1) to forced vital capacity (FVC) ratio \<0.7 * Resting arterial oxygen partial pressure at room air \>60 mmHg, according to recent (within a week) arterial blood gases assessment * Disease being stable and treated optimal, based on current GOLD guidelines. * Provision of informed written signed consent prior to study entry Exclusion Criteria: * Recent respiratory infection or exacerbation (as indicated by deterioration of respiratory symptoms, hospital admission and/or change in medication within the previous month), within the past 3 months * Changes in COPD medication with the past month * History of asthma and/or reversible airway obstruction (post bronchodilation FEV1/ FVC \>0.7) * Pulmonary hypertension * Congestive heart failure (Left Ventricle Ejection Fraction \<50% in recent echocardiography) * Severe peripheral artery disease * Chronic Kidney disease with eGFR \< 30 ml/min (KDIGO stages 3b, 4 ,5) * Active acute or chronic infectious diseases * Active malignant disease or hematologic disorder under treatment * History of neuromuscular disorder * History of severe intellectual disability or mental disorder * Any contradiction to moderate-high intensity exercise or cardiopulmonary exercise testing according to ATS/ACCP guidelines, such as: myocardial infarction within the past 6 months, unstable angina, syncope, symptomatic severe aortic stenosis, uncontrolled arrhythmias causing symptoms or hemodynamic compromise, acute pulmonary embolus or pulmonary infarction, thrombosis of lower extremities, suspected dissecting aneurysm, pulmonary edema, severe untreated arterial hypertension at rest (\> 200 mm Hg systolic, \> 120 mm Hg diastolic blood pressure), orthopedic impairment that compromises exercise performance.
Frequently Asked Questions
Who can join the NCT07707271 clinical trial?
This trial is open to participants of all sexes, studying COPD. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07707271 currently recruiting?
Yes, NCT07707271 is actively recruiting participants. Visit ClinicalTrials.gov or contact George Papanicolaou Hospital to inquire about joining.
Where is the NCT07707271 trial being conducted?
This trial is being conducted at Thessaloniki, Greece.
Who is sponsoring the NCT07707271 clinical trial?
NCT07707271 is sponsored by George Papanicolaou Hospital. The trial plans to enroll 12 participants.
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