NCT04379063.
Methods | Observational (longitudinal survey) |
Participants |
Study population: 10,000 Inclusion criteria: any physician who is currently practicing in Canada, whether they hold a full, provisional, or post‐graduate in‐training license Exclusion criteria: non‐physician healthcare providers, medical students, physicians without an active license to practice will be excluded |
Interventions | Not reported |
Outcomes |
Primary outcomes: MBI, HADS Secondary outcomes: PTSD checklist, PTGI‐SF Data collection: baseline and primary outcomes will be measured monthly until there is a month with no new cases; secondary outcomes will be measured monthly for the first 12 months. |
Notes | Trial registration: NCT04379063 Estimated completion date: May 2022 Further information should be sought from the author to get more details on the study design |