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Changes in Inflammatory Markers During Pulmonary Rehabilitation Based on Exacerbation States in COPD

Changes in Inflammatory Markers During Pulmonary Rehabilitation Based on Exacerbation States in COPD

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02740686
Acronym
CIMPRES-COPD
Enrollment
85
Registered
2016-04-15
Start date
2016-07-31
Completion date
2018-08-28
Last updated
2018-10-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Obstructive Pulmonary Disease

Keywords

COPD, Exercise, Immunity, Inflammation, Biomarkers

Brief summary

This study will examine the inflammatory response to exercise encompassed as part of a standard pulmonary rehabilitation programme in patients with chronic obstructive pulmonary disease (COPD). Patients will be split into two groups, frequent exacerbators or infrequent exacerbators, dependent upon exacerbation history to compare responses to pulmonary rehabilitation amongst phenotypes.

Detailed description

Pulmonary rehabilitation has been proven to benefit COPD patients in terms of quality of life and functional capabilities. The effects of pulmonary rehabilitation (exercise) on immune function are unclear despite clear benefits of exercise on immune function in healthy individuals being identified. Moderate-intensity and frequency of exercise has been shown to decrease the risk of upper respiratory tract infections in healthy individuals in comparison to sedentary individuals. Respiratory infections, also known as exacerbations, in COPD are the main cause of hospitalisation and mortality. Therefore, if exercise can modulate immune function in COPD, it can be encouraged further in COPD to reduce hospitalisation risk. However, it is important to compare the effects of exercise amongst different phenotypes as frequent exacerbators are known to have elevated inflammatory markers, and may consequently respond to exercise differently to infrequent exacerbators, paving a rationale for a different approach to this subset of patients.

Interventions

OTHERSample collection

Frequent exacerbators and infrequent exacerbators will have blood and sputum samples obtained around pulmonary rehabilitation. No other intervention will be administered. Healthy controls will have resting blood samples taken.

Sponsors

National Health Service, United Kingdom
CollaboratorOTHER_GOV
University of Lincoln
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
40 Years to 90 Years
Healthy volunteers
Yes

Inclusion criteria

* 58 frequent exacerbators and 58 infrequent exacerbators (116 in total) who have been diagnosed with any severity of COPD (according to BTS criteria, i.e. \>10 pack year smoking history and post bronchodilator spirometry FEV1/FVC ratio \<0.70 and FEV\<80%).

Exclusion criteria

* Inability or unwillingness to sign informed consent * Any unstable ongoing cardiovascular events which may be exacerbated by exercise * Inability to complete walk tests due to physical or mental impairment * Other active inflammatory conditions e.g. rheumatoid arthritis, cancer. * Known asthma, allergic rhinitis or other respiratory disease (bronchiectasis, pulmonary fibrosis) Healthy control group - Patients who have not been diagnosed with COPD or any other respiratory condition and are characteristically (age (between 45-85 years old) & smoking status) matched to recruited COPD patients.

Design outcomes

Primary

MeasureTime frame
Concentration of inflammatory markers in plasma and sputum (C-reactive protein, Fibrinogen, Interleukin(IL)-6, IL-8July 2016 - August 2018

Secondary

MeasureTime frame
Total and differential blood leukocyte countJuly 2016 - August 2018
Pre-activation and activation of blood neutrophils using flow cytometryJuly 2016 - August 2018
Pro-coagulant and pro-inflammatory microparticle signatures in plasmaJuly 2016 - August 2018
Changes in the expression of anti-inflammatory genesJuly 2016 - August 2018
Respiratory Symptoms™ (RS-Total score; RS-Breathlessness; RS-Cough and Sputum, and RS-Chest Symptoms)July 2016 - August 2018
Routine clinical outcome measures following pulmonary rehabilitation (completion rates and clinically important differences - ISWT, ESWT, 6MWD, CRQ)July 2016 - August 2018
Differences in basal levels of inflammation between frequent and infrequent exacerbators in comparison to healthy controlsJuly 2016 - August 2018
Severe, moderate and mild exacerbations (number of /days to defined events, severity, recovery)July 2016 - August 2018

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026