The NB Trauma Registry
The NB Trauma Registry (NBTR) captures epidemiological and hospital care data on injury patients admitted to designated trauma centers (levels I, II, and III) in New Brunswick, Canada. The objective of the NBTR is to collect data that can guide improvements in injury prevention, care, education, and research.
General Design
- Study design
- Registry
- Start - End Year
- 2014 -
- Number of Participants
- No Limit
Access
Availability of data and biosamples
Possible Access to Data | |
Possible Access to Biosamples | |
Other |
|
In addition to holding data within the NBTR, some data elements are promoted to New Brunswick Institute for Research, Data and Training (NB-IRDT). Metadata is available on the [NBTR website](https://nbtrauma.ca/healthcare-professionals/consensus-statements-resources/).
- On the study website : https://nbtrauma.ca/healthcare-professionals/tr...
Timeline
Population
NBTR population
The population is composed of patients with moderate to severe injuries who receive care at designated trauma centers in New Brunswick, Canada.
Selection Criteria
- Countries
-
- Canada
- Canadian Provinces
-
- New Brunswick
- Health Status
-
- Patients admitted to any of the eight designated trauma centres (levels I, II and III) for moderate to severe injuries.
Sources of Recruitment
- Specific Population
-
- Clinic patients
- Supplementary Information
-
Participating sites: Saint John Regional Hospital (level I), The Moncton Hospital (level II), Dr. Everett Chalmers Regional Hospital, Dr. Georges-L.-Dumont University Hospital Centre, Miramichi Regional Hospital, Edmundston Regional Hospital, Chaleur Regional Hospital, Campbellton Regional Hospital (level III).
Sample Size
- Number of Participants
- No Limit
Data Collection Events
# | Name | Data sources | Data sources - Biosamples | Start | End |
---|---|---|---|---|---|
0 | NBTR - Data Capture |
|
2014 | Ongoing |
Participating Studies
Acronym | Name | Study design | Countries |
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Harmonization Initiatives Included
Acronym | Name |
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Datasets
Name | Data Collection Events | Variables |
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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
No Areas of Information Collected
No Scales Collected
Areas of Information Collected per per Population and Data Collection Event
No Areas of Information Collected
No Scales Collected
Networks
Acronym | Name | Harmonization Initiatives | Individual Studies |
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Last Update: 2024-03-13T03:59:15.286