For Researchers
CanCOLD Data
With longitudinal evaluations and detailed characterization of study subjects using a range of assessment tools, CanCOLD is an invaluable resource to catalyze COPD research.
Profile
Overview
Access
Opportunities
Profile
Cohort Profile
CanCOLD is the first observational cohort specific to COPD having recruited its participants from the general population rather than more convenient recruitment in clinical settings. This strategy better mirrors prevalent COPD populations at large and provides proper representation of typically underrepresented groups in COPD studies; early disease, female population, individuals who have never smoked (up to 30% of the COPD population) and those with physician undiagnosed disease (up to 70% of the COPD population).
CanCOLD originated from the cross-sectional Burden of Obstructive Lung Disease (BOLD) study, an international initiative measuring the prevalence of COPD and its risk factors in different regions around the world, which included a data collection site in Vancouver, Canada. Expanding on this initiative nationally, the Canadian Obstructive Lung Disease (COLD) population-based prevalence study was established by randomly sampling a total of 6,551 non-institutionalized men and women aged ≥ 40 years from 9 Canadian cities: Vancouver, Montreal, Calgary, Quebec, Halifax, Toronto, Kingston, Saskatoon, and Ottawa.
With the aim of establishing a longitudinal population-based COPD cohort in Canada, COLD study participants within four target subsets were contacted to enroll in CanCOLD:
- Individuals with mild COPD (GOLD 1; post-bronchodilator FEV1/FVC<0.70 and FEV1≥80% predicted)
- Individuals with moderate-severe COPD (GOLD ≥2; post-bronchodilator FEV1/FVC<0.70 and FEV1<80% predicted)
- Sex and age matched (±2 years) ever-smokers without COPD
- Sex and age matched (±2 years) never-smokers without COPD
Data Collection Waves
At each data collection wave, trained CanCOLD research staff collect a deep pool of information that can be queried to address research questions related to COPD. A wide range of physical measures and assessment tools are used including anthropometric measures, validated questionnaires, blood samples, pulmonary function tests, cardiopulmonary exercise test (CPET) and multidetector computerized tomography scan (CT Scan).
Respiratory health is additionally evaluated by telephone contact every 3 months, when participants respond to a COPD exacerbation questionnaire, with questions on symptom changes, medication and health service use.
CanCOLD data can be linked to information held in provincial administrative and vital statistics databases such as health care utilization, medication intake, and cause of mortality. Finally, in order to assess the relationship of chronic respiratory disease development and progression with environmental factors such as ambient air pollution exposure and climate and weather events, data distributed by the Canadian Urban Environmental Health Research Consortium (CANUE) is linked to CanCOLD data.
COLD prevalence study N = 6551
2005 to 2016
Recruitment Sites
Vancouver | Montreal | Calgary |
n = 1552 | n = 1211 | n = 600 |
Quebec | Halifax | Toronto |
n = 586 | n = 549 | n = 541 |
Kingston | Saskatoon | Ottawa |
n = 533 | n = 504 | n = 475 |
COPD cases refused (n = 286)
or no contact (n = 266)
CanCOLD Visit 1 (baseline assessment) N=1561
2009 to 2015
Recruitment Sites
Vancouver | Montreal | Calgary |
n = 435 | n = 355 | n = 129 |
Quebec | Halifax | Toronto |
n = 85 | n = 127 | n = 74 |
Kingston | Saskatoon | Ottawa |
n = 136 | n = 104 | n = 116 |
Time lags between assessments
Median | Min | Max | |
CanCOLD v1 to v2 | 19 months | 6 months | 31 months |
CanCOLD v2 to v3 | 18 months | 3 months | 50 months |
CanCOLD v1 to v3 | 37 months | 24 months | 84 months |
CanCOLD v2 to v3 | 6 months | 3 months | 14 months |
CanCOLD Visit 2 N=1019
2011 to 2015
CanCOLD Visit 3 N=1198
2013 to 2019
CanCOLD Visit 4
2022 to 2023
Overview
Data Overview
At each data collection wave, trained CanCOLD research staff collect a deep pool of information that can be queried to address research questions related to COPD. Respiratory health is additionally evaluated by telephone contact every 3 months, when participants respond to a COPD exacerbation questionnaire. CanCOLD data can be linked to information held in provincial administrative and vital statistics databases as well as environmental exposure data distributed by the Canadian Urban Environmental Health Research Consortium (CANUE) is linked to CanCOLD data.
To explore all variables collected by the CanCOLD Study, please visit our Data Portal
Data Collection Wave | Measurements |
Visit 1 (Baseline) |
|
Visit 2 (18 months) |
|
Visit 3* (3 years) |
|
Visit 4 (10 years) |
|
Every 3 months | COPD exacerbation questionnaires (telephone/online) |
PFT – Pulmonary Function Test, CPET – Cardiopulmonary Exercise Test, CT Scan – multidetector computerized tomography scan, 6MWT – 6 Minute Walking Test
*Visit 3 PET, CPET, CTScan done on “at-risk” and COPD subjects only.
Access
Data Access
CanCOLD is a national and international resource offering opportunities to evaluate countless scientific hypotheses, to translate bench research to prevention and treatment, and to further insights into complex interactions of environment, lifestyle and genetics on chronic respiratory diseases including COPD. To achieve its objectives, the CanCOLD study makes its population-based longitudinal data available to Canadian and international investigators and trainees.
How to access our data?
Step 3
Address any requests for revisions from the Sustudy and Ancillary Study Committee.
Fees
CanCOLD charges data access fees to researchers on a partial cost-recovery basis. Data access fees help ensure the sustainability of the CanCOLD study, and help offset the costs of administration, coordination, and management of CanCOLD study activities. Data access fees also help partial recovery of CanCOLD database oversight, and of data extraction and delivery costs for a given project.
CanCOLD data access fees are primarily calculated based on:
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Funding source (i.e. private/industry sponsored vs. public/academic),
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Whether only one wave of data collection (cross-sectional study) or multiple data collection waves (longitudinal study) are requested,
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The types of data requested (i.e. questionnaires and spirometry, CPET, CT scan, and biomarker data), and
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The location of the primary applicants’ host institution (i.e. Canadian or international). Data access applications directly supporting a Masters or PhD thesis, or Post-doctoral fellowship project are subject to substantial discounts.
Opportunities
Training Opportunity
Training Opportunities CanCOLD serves to train future generations of clinicians, researchers, students and qualified research staff. As they become available, training opportunities will be listed below.
Coming Soon
Step 1
Visit our Data Portal. to learn more about the data CanCOLD collects.
Step 2
Create and submit a substudy proposal application via our Data Portal.
Step 3
Address any requests for revisions from the Substudy and Ancillary Study Committee.
Pas 1
Visitez notre portail de données pour en savoir plus sur les données que CanCOLD recueille.
Pas 2
Créez et soumettez une demande de proposition de sous-étude via notre portail de données.
Pas 3
Répondez à toute demande de révision du comité de révision (Substudy and Ancillary Study Committee (SASC)).