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Grant: Project Grant

Ottawa Hospital Research Institute

$126,225.00

Feasibility of Advance Consent for ParticipaTION in Acute Stroke Trials (ACTION)

EF 2022-23

Résumé
It is important to get a patient's permission (consent) to enroll them in research studies. However, stroke can happen so suddenly that patients are sometimes too sick to give their own consent. In this situation, researchers try to collect consent from family members or legal representatives on behalf of the patient. In some cases, researchers may enroll patients without their permission. We are trying to develop a way to get a patient's consent before they become too sick to provide it for themselves because we believe that patients should always be as involved as possible in the decision-making process. This new way is called advance consent and we are trying to see if patients who are at risk of having a stroke would agree to participate in a research study ahead of time in case they came back to the hospital in a situation where they were too sick to give consent. If we show that this program can work, we will expand our research to share our findings with stroke researchers around the world, and we hope that clinical trials will adopt this method to increase patients' involvement in stroke research. So far, we have asked doctors, ethicists and patients about what they think about advance consent. We are now ready to test our model of advance consent with stroke patients.
Programme
Project Grant
Emplacement
Ontario, Canada
Type de bénéficiaire
Other
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
479576
Name
Shamy Michel C
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Health Services and Policy Research
Theme2
Health systems / services
Prcname2
Humanities, Social Sciences, Law & Ethics in Health
Projecttitle
Feasibility of Advance Consent for ParticipaTION in Acute Stroke Trials (ACTION)
Programtype2
Operating Grants
Orgnameinp2
Ottawa Hospital Research Institute
Cihramount2
$126,225
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Clinical Trials; Consent; Ethics; Stroke
Abstract
It is important to get a patient's permission (consent) to enroll them in research studies. However, stroke can happen so suddenly that patients are sometimes too sick to give their own consent. In this situation, researchers try to collect consent from family members or legal representatives on behalf of the patient. In some cases, researchers may enroll patients without their permission. We are trying to develop a way to get a patient's consent before they become too sick to provide it for themselves because we believe that patients should always be as involved as possible in the decision-making process. This new way is called advance consent and we are trying to see if patients who are at risk of having a stroke would agree to participate in a research study ahead of time in case they came back to the hospital in a situation where they were too sick to give consent. If we show that this program can work, we will expand our research to share our findings with stroke researchers around the world, and we hope that clinical trials will adopt this method to increase patients' involvement in stroke research. So far, we have asked doctors, ethicists and patients about what they think about advance consent. We are now ready to test our model of advance consent with stroke patients.
Competitiondate
202303
Approvedterm2
1 yr 6 mths
Pinamesdelim
Shamy, Michel C; Dowlatshahi, Dariush
Approvedterm
1 an 6 mois
Cihrcontribution2
~ $126,225~ $0~