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Authors
McCabe, Erin https://orcid.org/0000-0003-3171-3065
Dyson, Michele
McNeil, Deborah
Hindmarch, Whitney
Ortega, Iliana
Arnold, Paul D.
Dimitropoulos, Gina
Clements, Ryan
Santana, Maria J.
Zwicker, Jennifer D.
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Funding
Funding for this research was provided by:
Alberta Children's Hospital Foundation
Canadian Institutes of Health Research, Mitacs, Alberta Health Services (Health System Impact Fellowship)
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Article History
Received: 15 March 2023
Accepted: 1 July 2024
First Online: 15 July 2024
Declarations
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: This study protocol was approved by The University of Calgary Research Ethics Boards (REB22-1137). Written consent to participate will be obtained from participants in the focus groups and interviews. Implied consent will be used for participants responding to the survey (i.e., by responding to the survey, participants are consenting to participate in research). Written consent to use of patient-reported outcome measures and clinical data for research will be obtained from patients and caregivers accessing Day Hospital and Intensive Community Treatment Services. Patients accessing walk-in services may be in crisis, therefore it would not be appropriate to ask for consent to use their clinical data for research at the time of their visit. Therefore, patients accessing walk-in services will be asked for consent to be contacted for research, and their consent to data use for research will be sought at a later date by a research team member.
: Not applicable.
: The authors declare that they have no competing interests.
