CClinicalTrials.gg
Status unknownNCT04796233Updated Sep 1, 2021

Patient Perspectives on Advance Care Planning Discussions Prior to Cardiac Surgery

An observational study in Cardiac Surgery, sponsored by University Health Network, Toronto. Status unknown at 1 site in Canada. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2021-09-01.

Sponsored by University Health Network, Toronto · Observational

The sponsor has not verified this record recently (last verified Feb 2021), so the status shown — last known as Not yet recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
40
Ages
18 Years and older
Sex
All
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Study summary

The purpose of this study is to explore patient perspectives on Advance Care Planning (ACP) prior to cardiac surgery, including perceptions of benefits, drawbacks, and barriers to ACP.

Read the detailed description

In this study, we plan to interview 40 patients who are scheduled to undergo cardiac surgery about their perspectives on preoperative ACP and discussion of their values, goals of care, and preferences for prolonged care in hospital prior to having surgery. We plan to conduct and audio record one-on-one interviews that are structured around standard questions about ACP. After recordings are completed, we plan to conduct an analysis of the interviews to find common themes and ideas that participants have about preoperative advance care planning. These results will help us understand whether patients value and wish to participate in advance care planning prior to major surgery, and will help to guide the structure and content of preoperative advance care plan programs in the future.

02

Conditions studied

  • Cardiac Surgery

Keywords

  • Advance Care Planning
03

In context

Lead sponsor

University Health Network, Toronto is the lead sponsor of 1,411 studies on the registry; 292 are open to participants now.

Of its 17 completed or terminated interventional studies of FDA-regulated products, 3 (18%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

We will enroll patients at Toronto General Hospital, a tertiary cardiac surgery centre in Toronto. We will include patients undergoing any cardiac surgery procedures that involve cardiopulmonary bypass, as well as patients undergoing off-pump coronary bypass procedures and any other high-risk cardiac surgery patients, for example, those undergoing ventricular assist device insertion or pericardectomy.

Inclusion criteria

  • Adult patients undergoing cardiac surgical procedures that involve a sternotomy, thoracotomy, or cardiopulmonary bypass for any indication.
  • Age > 18
  • English-speaking

Exclusion criteria

Exclusion Criteria:

  • Emergency surgery, regardless of indication or procedure
  • Minor/percutaneous cardiac procedure
  • Lack of decisional capacity due to dementia or other neurocognitive dysfunction
  • Previously decided upon advance care directives
  • Still considering surgery or not yet booked for an operation
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Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
40 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Interview

    Patient perspectives and attitudes regarding advance care planning (ACP) with a focus on patient values and goals prior to cardiac surgery.

    Time frame: 30-35 Minute interview

07

Study locations

1 site
  • Toronto General Hospital - University Health Network
    Toronto, Ontario M5G 2C4, Canada
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 1, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04796233
Lead sponsor
University Health Network, Toronto
Collaborators
Sunnybrook Health Sciences Centre
Responsible party
Sponsor
First posted
Mar 12, 2021
Start date
Oct 2021 (estimated)
Primary completion
Mar 2022 (estimated)
Completion
Mar 2023 (estimated)
Last update
Sep 1, 2021

Study contacts

Michael Tylee, MD
Contact
michael.tylee@uhn.ca
(416) 340-5164
Jo Carroll
Contact
jo.carroll@uhn.ca
416-340-4800 ext. 3243
Michael Tylee, MD
principal investigator · University Health Network, Toronto

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Feb 2021. You cannot join it, but the record below documents what was studied.

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