Chronic Obstructive Pulmonary Disease Clinical Trial
— T-RexOfficial title:
Activation of Regenerative Pathways by Exercise Training in Patients With Chronic Obstructive Pulmonary Disease
Verified date | March 2024 |
Source | Uppsala University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The main objective of this project is to identify mechanisms for lung regeneration in patients with COPD induced by exercise training. The hypothesis is that adjusted exercise training improves disease outcome in these patients by decrease remodelling processes linked to oxidative stress, inflammatory and/or immunological pathways in the lung. Along the way, the investigator also expect to identify (or validate) biomarkers mirroring systemic processes such as reduced inflammation and ameliorating the epithelial barrier in these patients. These events may additionally act as potential targets for interventions. Objectives (i) Evaluate biomarkers for regenerative processes, matrix turnover, stem cell activity and inflammatory patterns in lung tissue biopsies, blood- and urine samples correlated to vital lung parameters and physical capacity, before and after attending an exercise-training program. (ii) Study the effects of exercise training on the pulmonary ventilation/perfusion ratio and quality of life. (iii) Evaluate the relation between pathophysiology in the lung evaluated by CT scan, and systemic response measured by muscle biopsies and biomarkers in blood/urine. (iv) Investigate in vitro cell behaviour and remodelling/regenerative processes altered in COPD patients upon exercise training (aim 1).
Status | Recruiting |
Enrollment | 80 |
Est. completion date | April 30, 2025 |
Est. primary completion date | February 28, 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 50 Years to 85 Years |
Eligibility | Inclusion Criteria: - Forced expiratory volume in one second (FEV1) 85-30 % of predicted post bronchodilator - Optimal medical treatment according to GOLD and the Swedish National Guidelines - Absence of other significant diseases that could contribute to physical exercise limitation - Non-smoking since at least one year - Free from exacerbations (last 4 weeks) - BMI = 18- 35 Exclusion Criteria: - Regular participation in adjusted/specially designed exercise sessions - Unstable cardiovascular or pulmonary disease - Smoking - Any other criteria that at the discretion of the investigator prevent the study subject from participating in an exercise-training program |
Country | Name | City | State |
---|---|---|---|
Sweden | Lund University | Lund | |
Sweden | Uppsala University | Uppsala |
Lead Sponsor | Collaborator |
---|---|
Uppsala University | Lund University |
Sweden,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Pulmonary Function | FEV1 (Forced Expiratory volume in one second) | Baseline, post intervention at 12 wks | |
Secondary | Physical capacity | 6MWD (six-minute walk distance), longer distance = better health | Baseline, post intervention at 12 wks | |
Secondary | Inflammation markers | Biomarkers (eg. C reactive protein, Interleukin-6) | Baseline, post intervention at 12 wks | |
Secondary | Level of emphysema | HRCT, (high-resolution computed tomography), AiDA (Air space dimension assessment) | Baseline, post intervention at 12 wks | |
Secondary | Maximal physical capacity ( Wmax) | Maximal watt during incremental cardiopulmonary exercise test | Baseline, post intervention at 12 wks | |
Secondary | COPD Assessment Test (CAT) | Health status, Score 1-40, lower score = better health | Baseline, post intervention at 12 wks |
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