The Continuing Care Reporting System
Overview
- Acronym
- CCRS
- Website
- CCRS
- Contacts
General Design
- Study design
- Registry
- Start - End Year
- 1973 -
- General Information on Follow Up (profile, frequency)
-
Participant information is updated every time they access hospital-based or residential-based continuing care facilities.
- Recruitment Target
-
- Individuals
- Number of Participants
- No Limit
Access
Availability of data and biosamples
| Possible Access to Data | |
| Possible Access to Biosamples | |
| Other |
|
National-level databases at CIHI derive from information provided by the jurisdications (provinces and territories). However, not all jurisdictions provide data to CIHI for all the national databases. Search the CIHI website (https://www.cihi.ca/en) for the specific database of interest to identify which jurisdictions are included in the national-level database. But also note that jurisdictions that do not send specific data to CIHI may still have local versions; check with those jurisdications for further information. * Alberta https://www.alberta.ca/health-research.aspx#jumplinks-3 * British Columbia https://www.popdata.bc.ca/data_access * Manitoba https://umanitoba.ca/manitoba-centre-for-health-policy/data-repository * New Brunswick https://www.unb.ca/nbirdt/data/access/index.html * Newfoundland https://www.nlchi.nl.ca/index.php/quality-information/information-requests * Nova Scotia https://medicine.dal.ca/departments/department-sites/community-health/research/hdns/services/data-access-guidelines.html * Ontario https://www.ontariohealth.ca/about-us/governance-accountability/open-data * Saskatchewan https://www.ehealthsask.ca/health-data/analytics/Pages/Researcher-Access-to-Data.aspx * Yukon https://yukon.ca/en/access-government-information
Supplementary Information
Timeline
Population
Selection Criteria
- Countries
-
- Canada
- Canadian Provinces
-
- Alberta
- British Columbia
- Manitoba
- New Brunswick
- Newfoundland and Labrador
- Nova Scotia
- Ontario
- Saskatchewan
- Yukon
- Other Criteria
- Participants are admitted to, assessed in or discharged from hospital-based or residential-based continuing care facilities.
Sources of Recruitment
- Specific Population
-
- Clinic patients
- Supplementary Information
-
Registry participants are selected by default when they access hospitals with continuing care beds (extended, auxiliary, chronic or complex care beds) or residential care facilities (nursing homes, personal care homes or long-term care facilities).
Sample Size
- Number of Participants
- No Limit
Data Collection Events
| # | Name | Data sources | Data sources - Biosamples | Start | End |
|---|---|---|---|---|---|
| 0 | CCRS - Health Service Utilization |
|
1973 | 2021 | |
| 1 | CCRS - Health Assessments |
|
2011 | 2021 |
Participating Studies
| Acronym | Name | Study design | Countries |
|---|
Harmonization Initiatives Included
| Acronym | Name |
|---|
Datasets
| Name | Data Collection Events | Variables |
|---|
Areas of Information Collected
- Socio-demographic and economic characteristics
- Death
- Lifestyle and behaviours
- Physical measures and assessments
- Birth, pregnancy and reproductive health history
- Laboratory measures
- Perception of health, quality of life, development and functional limitations
- Cognition, personality and psychological measures and assessments
- Diseases
- Life events, life plans, beliefs and values
- Symptoms and signs
- Preschool, school and work life
- Medication and supplements
- Social environment and relationships
- Non-pharmacological interventions
- Physical environment
- Health and community care services utilization
- Administrative information
Variables Content Summary
Areas of Information Collected
Areas of Information Collected per per Population and Data Collection Event
Networks
| Acronym | Name | Harmonization Initiatives | Individual Studies |
|---|