Actively Recruiting

Phase Not Applicable
Age: 60Years +
All Genders
Healthy Volunteers
NCT06068322

Supramaximal High-Intensity Interval Training in People With and Without Chronic Obstructive Pulmonary Disease

Led by Umeå University · Updated on 2024-05-23

208

Participants Needed

2

Research Sites

264 weeks

Total Duration

On this page

Sponsors

U

Umeå University

Lead Sponsor

H

Hasselt University

Collaborating Sponsor

AI-Summary

What this Trial Is About

Beyond pulmonary complications, COPD presents with extrapulmonary manifestations including reduced cognitive, cardiovascular, and muscle function. While exercise training is the cornerstone in the non-pharmacological treatment of COPD, there is a need for new exercise training methods. The COPD-HIIT trial intend to investigate the effects and mechanisms of 12 weeks supramaximal high-intensity interval-training (HIIT) compared to moderate intensive continous training (MICT) in people with COPD and matched healthy controls on important clinical outcomes. The trial also intends to compare the effects of 24 months of exercise training (supramaximal HIIT or MICT) to usual care in people with COPD on brain health, cardiorespiratory fitness and muscle power; in people with COPD.

CONDITIONS

Official Title

Supramaximal High-Intensity Interval Training in People With and Without Chronic Obstructive Pulmonary Disease

Who Can Participate

Age: 60Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • 60 years of age or older
  • Independent in activities of daily living
  • For people with COPD: Symptomatic with COPD assessment test score 6 or modified Medical Research Council dyspnea scale score 2 or not regularly physically active at moderate or high intensity over the last year
  • For people with COPD: Confirmed COPD diagnosis by post-bronchodilator spirometry with FEV1/FVC ratio < 0.70
  • For healthy controls: Normal lung function
Not Eligible

You will not qualify if you...

  • Unstable movement-related, cardiovascular, neuromuscular, metabolic, skeletal, or rheumatic conditions that prevent exercise or tests
  • Musculoskeletal pain that prevents exercise or testing
  • Recent heart events such as myocardial infarction, bypass surgery, or angioplasty
  • Uncontrolled high blood pressure
  • Abnormal ECG findings during exercise test
  • Other lung diseases like asthma, interstitial lung disease, lung cancer, pulmonary hypertension, or pulmonary fibrosis
  • Medical conditions or treatments affecting brain function or cognition, including head trauma, neurological diseases, severe cognitive impairment, recent or current cancer treatment
  • MRI or PET/CT contraindications such as metal implants or claustrophobia
  • Inability to read or speak Swedish (Ume� University participants), Dutch or French (Hasselt University participants), or English
  • For COPD patients: Co-morbidities limiting exercise more than COPD
  • Currently or recently (past 12 months) in pulmonary rehabilitation
  • Recent COPD exacerbation requiring medication change within six weeks

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Hasselt University

Hasselt, Diepenbeek, Belgium, 3590

Actively Recruiting

2

Umeå University

Umeå, Sweden

Actively Recruiting

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Research Team

A

André Nyberg, PhD

CONTACT

J

Johan Jakobsson, M.Sc.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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