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Study identifier: NCT06168474 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Evaluating Simplified Layered Consent for Clinical Trials

Condition: Staphylococcus Aureus Bacteremia  ·  Sponsor: Sunnybrook Health Sciences Centre

PhaseNA
Planned participants346
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNo

About this study

The goal of this clinical trial (the SIMPLY-SNAP trial) is to compare a simplified layered consent form to a full-length consent form for use during the informed consent process for a larger clinical trial of treatment of Staphylococcus aureus bloodstream infection (the SNAP trial). The main questions it aims to answer are: * Does use of a simplified layered consent form lead to an increased recruitment rate to the SNAP trial? * Does use of a simplified layer consent form lead to increased participant understanding of the SNAP trial and increased participant satisfaction with the informed consent process? Participants will be randomized to either the full-length informed consent form or the simplified layered consent form containing links to optional supplementary information or videos. Research staff will use the assigned form to explain the SNAP trial to participants. After consent, participants will be evaluated on their understanding of the SNAP trial and satisfaction with the consent process using a questionnaire.

This description comes directly from the study's public registry record.

Talk to the study team

Sean WX Ong, MBBS  ·  4164806100  ·  s.ong@mail.utoronto.ca

Always discuss trial participation with your own doctor first.

Locations (6)

University of Calgary, Foothills Medical Centre, Peter Lougheed Centre, Rockyview Hospital, South Health CampusCalgary, Alberta, CanadaRecruiting
Hamilton General HospitalHamilton, Ontario, CanadaRecruiting
The Ottawa HospitalOttawa, Ontario, CanadaRecruiting
Sunnybrook Health Sciences CentreToronto, Ontario, CanadaRecruiting
Montreal General HospitalMontreal, Quebec, CanadaRecruiting
Royal Victoria HospitalQuébec, Quebec, CanadaRecruiting

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Source record: clinicaltrials.gov/study/NCT06168474