Evaluating Treatable Traits Across the Spectrum of Chronic Obstructive Airways Disease

Sponsor
University of Leeds (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05976919
Collaborator
The Leeds Teaching Hospitals NHS Trust (Other)
100
24

Study Details

Study Description

Brief Summary

Respiratory disease affects one in five people and is a leading cause of global morbidity and mortality. Chronic obstructive airways diseases encompass conditions characterised by expiratory airflow limitation, exertional dyspnoea, activity limitation and impaired quality of life. The most common conditions include chronic obstructive pulmonary disease (COPD), asthma, bronchiectasis, cystic fibrosis and primary ciliary dyskinesia. In recent years, there has been concerted effort in the scientific and respiratory medicine community to improve the diagnosis and management of chronic obstructive airways diseases using personalised or precision medicine (i.e., tailoring therapies and interventions according to specific "treatable traits") and identifying phenotypes or endotypes using validated biomarkers. To date, however, research in this setting has primarily focussed on people with COPD and asthma, with limited studies in other forms of chronic obstructive airways diseases. The aim of this study is therefore two-fold; first, to compare pulmonary physiology (i.e., large and small airway involvement) and extra-pulmonary manifestations across the spectrum of chronic obstructive airways, and second, to determine how disease-specific treatable traits associate with physical activity and health-related quality of life.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Pulmonary function testing

Study Design

Study Type:
Observational
Anticipated Enrollment :
100 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Evaluating Treatable Traits Across the Spectrum of Chronic Obstructive Airways Disease
Anticipated Study Start Date :
Aug 1, 2023
Anticipated Primary Completion Date :
Jul 31, 2025
Anticipated Study Completion Date :
Jul 31, 2025

Arms and Interventions

Arm Intervention/Treatment
COPD

Diagnostic Test: Pulmonary function testing
Physiological assessment of pulmonary physiology (large and small airways), exercise capacity, physical activity and body composition.
Other Names:
  • Cardiopulmonary exercise testing
  • Physical activity (daily step count)
  • Dual-energy X-ray absorptiometry (body composition)
  • Asthma

    Diagnostic Test: Pulmonary function testing
    Physiological assessment of pulmonary physiology (large and small airways), exercise capacity, physical activity and body composition.
    Other Names:
  • Cardiopulmonary exercise testing
  • Physical activity (daily step count)
  • Dual-energy X-ray absorptiometry (body composition)
  • Bronchiectasis

    Diagnostic Test: Pulmonary function testing
    Physiological assessment of pulmonary physiology (large and small airways), exercise capacity, physical activity and body composition.
    Other Names:
  • Cardiopulmonary exercise testing
  • Physical activity (daily step count)
  • Dual-energy X-ray absorptiometry (body composition)
  • Cystic fibrosis

    Diagnostic Test: Pulmonary function testing
    Physiological assessment of pulmonary physiology (large and small airways), exercise capacity, physical activity and body composition.
    Other Names:
  • Cardiopulmonary exercise testing
  • Physical activity (daily step count)
  • Dual-energy X-ray absorptiometry (body composition)
  • Primary ciliary dyskinesia

    Diagnostic Test: Pulmonary function testing
    Physiological assessment of pulmonary physiology (large and small airways), exercise capacity, physical activity and body composition.
    Other Names:
  • Cardiopulmonary exercise testing
  • Physical activity (daily step count)
  • Dual-energy X-ray absorptiometry (body composition)
  • Outcome Measures

    Primary Outcome Measures

    1. Physical activity [7 day period]

      Step-count

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Inclusion Criteria:
    • Prior diagnosis of airways disease in accordance with European Respiratory Society guidelines.

    • Non / ex-smokers (packs recorded as cigarettes per day / years smoked).

    • Male or female aged 18-65 years

    • Ability to provide written informed consent.

    • Full comprehension of spoken and written English language.

    • Cystic Fibrosis patients on triple CFTR modulators (90% cohort)

    • Cystic Fibrosis patients on no CFTR modulators

    • Healthy controls - entirely asymptomatic, no prior history of inhaler medication use and free from respiratory disease.

    Exclusion Criteria:
    • Severe exacerbation requiring hospital admission or oral corticosteroids (OCS) in the past two months.

    • Absolute or relative contraindications to cardio-pulmonary exercise testing or submaximal exercise testing.

    • Absolute or relative contraindications to pulmonary function testing .

    • Absolute or relative contraindications to dual energy x-ray (DEXA) scanning (i.e., pregnancy, recent contrast media administration or subject weight).

    • Non-ambulant or musculoskeletal impairment that may affect activities of daily living or maximal exercise testing.

    • Significant cognitive impairment (i.e., unable to provide written informed consent or safely / successfully perform tests).

    • Currently receiving oxygen therapy.

    • Inability to consent.

    • Burkholderia Cepacia Complex, mycobacterium tuberculosis or mycobacterium abseccus infection.

    • Lung transplantation

    • Diagnosis of cardiovascular disease.

    • Abnormal blood screening (anaemia, moderate / severe renal failure etc.)

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • University of Leeds
    • The Leeds Teaching Hospitals NHS Trust

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Dr Oliver Price, Principal Investigator, University of Leeds
    ClinicalTrials.gov Identifier:
    NCT05976919
    Other Study ID Numbers:
    • 323694
    First Posted:
    Aug 4, 2023
    Last Update Posted:
    Aug 8, 2023
    Last Verified:
    Aug 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 8, 2023