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The Vancouver-BOLD Study: The Burden of Chronic Obstructive Lung Disease

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified January 2013 by University of British Columbia.
Recruitment status was:  Active, not recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT00136006
First Posted: August 26, 2005
Last Update Posted: February 1, 2013
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
University of British Columbia
  Purpose
This is a study of the lung health of the population of Vancouver and the extent of, and the risk factors for, chronic obstructive lung disease.

Condition Intervention
Chronic Obstructive Lung Disease Behavioral: Study to determine the burden of disease

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Retrospective
Official Title: The Burden of Chronic Obstructive Lung Disease (BOLD) Study

Resource links provided by NLM:


Further study details as provided by University of British Columbia:

Primary Outcome Measures:
  • Lung health [ Time Frame: 10 years ]
    Lung health of the population of Vancouver and the extent of, and the risk factors for, chronic obstructive lung disease


Estimated Enrollment: 1000
Study Start Date: August 2005
Estimated Study Completion Date: December 2013
Estimated Primary Completion Date: December 2013 (Final data collection date for primary outcome measure)
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   40 Years to 90 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Population of Vancouver, BC, Canada
Criteria

Inclusion Criteria:

  • 40 years of age and older
  • Both sexes
  • Random sample of population

Exclusion Criteria:

  • Contraindication for lung function testing and serious life threatening illness.
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00136006


Locations
Canada, British Columbia
St.Paul's Hospital/Providence Health Care
Vancouver, British Columbia, Canada, V5Z 1L8
Sponsors and Collaborators
University of British Columbia
Investigators
Study Director: Wen Wang University of British Columbia
  More Information

Responsible Party: University of British Columbia
ClinicalTrials.gov Identifier: NCT00136006     History of Changes
Other Study ID Numbers: P05-0061
05-0965
First Submitted: August 25, 2005
First Posted: August 26, 2005
Last Update Posted: February 1, 2013
Last Verified: January 2013

Keywords provided by University of British Columbia:
Epidemiology
Lung health
lung function
COPD

Additional relevant MeSH terms:
Lung Diseases
Lung Diseases, Obstructive
Pulmonary Disease, Chronic Obstructive
Respiratory Tract Diseases