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Association of Physical Activity Levels and Inflammatory Markers Following Pulmonary Rehabilitation (PALI-COPD)

U

University of Lincoln

Status

Completed

Conditions

COPD

Treatments

Other: Physical activity monitoring

Study type

Observational

Funder types

Other

Identifiers

NCT03455153
18/WM/0081

Details and patient eligibility

About

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.

Enrollment

18 patients

Sex

All

Ages

40 to 90 years old

Volunteers

No Healthy Volunteers

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).

Trial design

18 participants in 2 patient groups

Most active
Description:
COPD patients with higher physical activity levels as defined by daily step counts.
Treatment:
Other: Physical activity monitoring
Least active
Description:
COPD patients with lower physical activity levels as defined by daily step counts.
Treatment:
Other: Physical activity monitoring

Trial contacts and locations

3

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Data sourced from clinicaltrials.gov

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