The Canadian Cohort Obstructive Lung Disease

NCT00920348 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 1500

Last updated 2018-08-27

No results posted yet for this study

Summary

Abstract Chronic obstructive pulmonary disease (COPD) is the fourth leading cause of death in Canada. COPD is not just a disease of men, nor is it solely a disease in old age. Women have been underrepresented and early disease has not been studied. Underdiagnosis of COPD remains a significant problem, and it may indicate an unmet healthcare need. This can potentially results not only in a patient been misinformed, but can lead to incorrect management.

Epidemiological research is needed to develop a framework to combat this major health problem, by better characterization of the population of men and women at risk and patients with early disease, by better understanding which factors modifiable through health interventions are related to health perception (health-related quality of life) and disease evolution.

This will be possible through a nationwide study, the Canadian Cohort Obstructive Lung disease (CanCOLD), a prospective longitudinal study. The CanCOLD study is built on the current ongoing prevalence nationwide study, the Canadian Obstructive Lung disease "COLD" study.

The CanCOLD will be the first study to assess prevalence of disease across Canada and its consequence in men and women, and to evaluate a conceptual model of disease severity based on patient's health perception (health-related quality of life). Ultimately, this project will extend to a longitudinal follow up (3 years or beyond) and will allow to have a better understanding of the lifestyle risk factors, not only smoking but also diet, physical activity, and co morbid conditions. This will be a great asset to shift from management of a single risk factor (tobacco control) to total COPD risk management. The results of the study will greatly help to assist decision makers in developing policies to improve the diagnosis, the management of COPD and to optimize health care services use.

Conditions

Sponsors & Collaborators

  • Canadian Institutes of Health Research (CIHR)

    collaborator OTHER_GOV
  • GlaxoSmithKline

    collaborator INDUSTRY
  • AstraZeneca

    collaborator INDUSTRY
  • Pfizer

    collaborator INDUSTRY
  • Boehringer Ingelheim

    collaborator INDUSTRY
  • Novartis

    collaborator INDUSTRY
  • Takeda

    collaborator INDUSTRY
  • Merck Sharp & Dohme LLC

    collaborator INDUSTRY
  • Almirall, SAS

    collaborator INDUSTRY
  • McGill University Health Centre/Research Institute of the McGill University Health Centre

    lead OTHER

Principal Investigators

  • Jean Bourbeau, M.D., M.Sc. · McGill University Health Centre/Research Institute of the McGill University Health Centre

  • Wan Tan, M.D. · CAAA University of British Columbia

  • François Maltais, M.D. · CFBA Université Laval

  • Shawn Aaron, M.D., M.Sc. · OHGC Ottawa Hospital General Campus

  • Denis O'Donnell, M.D. · CEDA Queen's University (Kinsgston)

  • Darcy D Marciniuk, M.D. · CCAA University of Saskatchewan

  • Robert Cowie, M.D. · CBBA University of Calgary

  • Kenneth R. Chapman, M.D., M.Sc. · CEAA University of Toronto

  • Paul Hernandez, M.D. · CHAA Dalhousie University (Nova Scotia)

  • Mark J. FitzGerald, M.D. · CAAA University of British Columbia

  • Donald Sin, M.D. · CAAA University of British Columbia

  • Andrea Benedetti, Ph.D. · INUD McGill University Healty Center

  • Yves Lacasse, M.D., M.Sc. · CPVR Institut universitaire de cardiologie et de pneumologie de Québec

  • Pierre Ernst, M.D. · McGill University

  • Harvey Coxson, M.D. · University of British Columbia

  • Roger Goldstein, M.D. · CEAA University of Toronto

  • Carlo Marra, Ph.D. · CAAA University of British Columbia

Eligibility

Min Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-01-31
Primary Completion
2022-12-31
Completion
2022-12-31

Countries

  • Canada

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00920348 on ClinicalTrials.gov