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Association of Physical Activity Levels and Inflammatory Markers Following Pulmonary Rehabilitation

The Association of Physical Activity Levels and Inflammatory Markers in COPD Patients Following Pulmonary Rehabilitation

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03455153
Acronym
PALI-COPD
Enrollment
18
Registered
2018-03-06
Start date
2018-05-02
Completion date
2018-10-02
Last updated
2018-10-09

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

Conditions

COPD

Keywords

Pulmonary Rehabilitation, Neutrophils

Brief summary

COPD is characterised by irreversible airflow limitation that is usually progressive and associated with an enhanced chronic inflammatory response. This inflammation can be amplified with flare-ups that are commonly seen in COPD patients. Pulmonary rehabilitation is one of the most effective methods of managing chronic obstructive pulmonary disease (COPD). Pulmonary rehabilitation has been seen to induce improvements in functional capacity and quality. In healthy individuals, exercise has been shown to induce an anti-inflammatory response when performed regularly. However, the effects of exercise on inflammation in COPD are unclear. Our initial CIMPRES-COPD study has looked into the effects of short-term exercise, as part of pulmonary rehabilitation, on inflammation. However, this trial will examine the inflammatory response in COPD patients who are most active following pulmonary rehabilitation against those who are least active. This study will split participants into 2 groups according to physical activity level following pulmonary rehabilitation. We will recruit 40 COPD patients who provided a sample in the initial CIMPRES-COPD study to explore inflammatory responses in those who are most active and least active. By better understanding the mechanisms of how long-term physical activity levels affects inflammation in COPD, we could design better interventions to increase physical activity levels following pulmonary rehabilitation.

Interventions

COPD patients will wear an accelerometer and complete questionnaires related to daily physical activity levels for 7 days before returning for a clinic visit.

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
No

Inclusion criteria

* Patients diagnosed with any severity of COPD (according to British Thoracic Society criteria, i.e. \>10 pack year smoking history and post bronchodilator spirometry FEV1/FVC ratio \<0.70 and FEV\<80%) * Previously enrolled on pulmonary rehabilitation providing at least one sample for the CIMPRES-COPD trial.

Exclusion criteria

* Any unstable ongoing cardiovascular events. * Other active inflammatory conditions (e.g. rheumatoid arthritis, cancer). * Known asthma, allergic rhinitis or other respiratory disease (bronchiectasis, pulmonary fibrosis).

Design outcomes

Primary

MeasureTime frameDescription
CytokinesMay 2018 - August 2018Changes in concentration of inflammatory cytokines in the plasma of all participants using ELISA's (mg/L)

Secondary

MeasureTime frameDescription
Leukocyte countMay 2018 - August 2018Changes in total and differential leukocyte count in all participants (10\^9.L-1)
Cell functionMay 2018 - August 2018Changes in function of the following cells: myeloperoxidase, neutrophil elastase, MMP-8, MMP-9, TNF-a in the plasma of all participants using ELISA's (mg/L)
Cell sensitivity to corticosteroidsMay 2018 - August 2018Changes in cell sensitivity to corticosteroids and forskolin in all participants (expressed as fold increase from not treated samples)

Countries

United Kingdom

Outcome results

None listed

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