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The Effects of Aerobic Exercise Training on Vascular, Cardiac and Cerebral Vascular Function in COPD

17 août 2016 mis à jour par: University of British Columbia

The Effects of Aerobic Exercise Training on Peripheral Vascular, Cardiac and Cerebral Vascular Function in Patients With Chronic Obstructive Pulmonary Disease

The primary cause of chronic obstructive pulmonary disease is smoking, which can lead to inflammation in the lungs and blood vessels that can lead to secondary problems such as blood vessel disease, high blood pressure and heart disease. Aerobic exercise training has been shown to reduce the risk of heart and brain disease; however, it is currently unknown whether exercise training can have the same affect in patients with COPD. The aim of this study is to investigate how eight weeks of aerobic exercise training improves blood vessel and heart function and brain blood flow in patients with COPD.

Aperçu de l'étude

Description détaillée

Chronic obstructive pulmonary disease (COPD) is a treatable respiratory condition that is only partially reversible. The primary cause of COPD is smoking which leads to airway inflammation and oxidative damage to the lungs, which has been linked to the development and progression of the disease. The inflammation is not isolated to the lungs as patients with COPD also have systemic inflammation that has been linked to a number of cardiovascular comorbidities such as endothelial dysfunction, cardiovascular disease and stroke. Evidence demonstrates that COPD patients have a greater incidence of vascular dysfunction and adverse vascular remodeling, which worsens with disease severity. In fact, patients with COPD are at 35 times greater risk of developing cardiovascular disease and stroke than healthy aged matched individuals. In healthy individuals and a number of chronic conditions, aerobic exercise training is well established to reduce the risk of cardiovascular and cerebrovascular disease. The benefits of exercise are likely through improvements in endothelial function, systemic inflammation, and cardiac and cerebral vascular function. However, whether exercise training can have the same effects in a chronic inflammatory condition like COPD has not been studied. The purpose of this study is to determine the effectiveness of an 8 week aerobic exercise training program in patient's chronic obstructive pulmonary disease as determined by improvements in endothelial function, systemic inflammation and cardiac and cerebral vascular function.

Type d'étude

Interventionnel

Inscription (Réel)

58

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

    • British Columbia
      • Kelowna, British Columbia, Canada, V1V 1V7
        • University of British Columbia

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

40 ans à 80 ans (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Oui

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

  • Non-smokers (>6 months);
  • Forced expiratory volume in one second/ forced vital capacity (FEV1/FVC) < 0.7 and FEV1/FVC <lower limit of normal
  • Stable (>3 months exacerbation free)

Exclusion Criteria:

  • On supplemental oxygen;
  • Known cardiac or cerebral vascular disease, diabetes, obstructive sleep apnea;
  • Uncontrolled hypertension;
  • BMI >30kg/m2
  • Currently performing pulmonary rehabilitation or structured exercise training;
  • Desaturate during exercise (SpO2<85%)
  • Cardiovascular contraindications to exercise in the incremental test used for screening

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Non randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Seul

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Patients with COPD
Stable patients with COPD participated in an 8-week (24 session) individualized, non-linear aerobic exercise training program consisting of upper and lower body cycle ergometry.
Aerobic exercise performed on lower body stationary ergometer and an upper extremity arm crank. Intensity (50-95% workload maximum) and durations (20-45 min) are fluctuated daily to optimize training stress and adaptation
Comparateur actif: Healthy Controls
Age, sex, BMI and activity matched controls participated in an 8-week (24 session) individualized, non-linear aerobic exercise training program consisting of upper and lower body cycle ergometry.
Aerobic exercise performed on lower body stationary ergometer and an upper extremity arm crank. Intensity (50-95% workload maximum) and durations (20-45 min) are fluctuated daily to optimize training stress and adaptation

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Endothelial Function
Délai: 8-weeks (following 24 sessions of exercise training)
The change in brachial artery flow mediated dilation measured using reactive hyperaemia
8-weeks (following 24 sessions of exercise training)

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Arterial Stiffness
Délai: 8-weeks (following 24 sessions of exercise training)
The change in pulse wave velocity measured using tonometry
8-weeks (following 24 sessions of exercise training)
Carotid intima-medial thickness
Délai: 8-weeks (following 24 sessions of exercise training)
The change in carotid intima-medial thickness measured by ultrasound
8-weeks (following 24 sessions of exercise training)
Carotid Compliance
Délai: 8-weeks (following 24 sessions of exercise training)
The change in carotid compliance measured using tonometry and ultrasound for the carotid arteries
8-weeks (following 24 sessions of exercise training)
Inflammatory Biomarkers
Délai: 8-weeks (following 24 sessions of exercise training)
The change in serum levels of CRP, IL-6, IL-10 and TNF-alpha measured using Luminex multiplex bead-based technology
8-weeks (following 24 sessions of exercise training)
Systolic function
Délai: 8-weeks (following 24 sessions of exercise training)
The change in stroke volume using echocardiography
8-weeks (following 24 sessions of exercise training)
Diastolic function
Délai: 8-weeks (following 24 sessions of exercise training)
The change in left ventricular end-diastolic volume using echocardiography
8-weeks (following 24 sessions of exercise training)
Cerebral Blood Flow
Délai: 8-weeks (following 24 sessions of exercise training)
The change in cerebral and neck blood flow using ultrasound
8-weeks (following 24 sessions of exercise training)
Cerebrovascular Reactivity
Délai: 8-weeks (following 24 sessions of exercise training)
The change in middle cerebral artery velocity in response to carbon dioxide
8-weeks (following 24 sessions of exercise training)
Cerebrovascular Autoregulation
Délai: 8-weeks (following 24 sessions of exercise training)
The change in phase delay measured by transfer function analysis
8-weeks (following 24 sessions of exercise training)

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Les enquêteurs

  • Chercheur principal: Neil Eves, PhD, University of British Columbia

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

Publications générales

  • Gelinas JC, Lewis NC, Harper MI, Ainslie PN, Rolf JD, Eves ND. Aerobic Exercise Training on Peripheral Vascular Structure and Function in Patients with Chronic Obstructive Pulmonary Disease. American Journal of Respiratory and Critical Care Medicine, 191:A5305, 2015.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude

1 janvier 2012

Achèvement primaire (Réel)

1 mai 2015

Achèvement de l'étude (Réel)

1 mai 2015

Dates d'inscription aux études

Première soumission

4 août 2016

Première soumission répondant aux critères de contrôle qualité

17 août 2016

Première publication (Estimation)

23 août 2016

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Estimation)

23 août 2016

Dernière mise à jour soumise répondant aux critères de contrôle qualité

17 août 2016

Dernière vérification

1 août 2016

Plus d'information

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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