ClinicalTrials.Veeva

Menu

Prehabilitation Program for Patients Awaiting Elective Heart Surgery at Increased Risk of Postoperative Complications: Feasibility and Potential Clinical Outcomes (PRÉAD-CARDIAQU)

U

University of Montreal

Status

Not yet enrolling

Conditions

Postoperative Complications
Cardiac Surgery
Prehabilitation

Treatments

Other: Exercise

Study type

Interventional

Funder types

Other

Identifiers

NCT07144722
2025-3527

Details and patient eligibility

About

The goal of this study is to learn if an exercise-based prehabilitation program can help people who are waiting for heart surgery and are at higher risk of complications recover better.

The main questions it aims to answer are:

Can a home-based prehabilitation program prescribed by a physiotherapist be done safely and realistically before heart surgery?

Participants will:

Take part in a personalized exercise program for a 8 to 16 weeks before surgery

Do breathing muscle training at home

Meet with a physiotherapist once a week, either in person or by video call

Be assessed before and after the program

Researchers will compare the postoperative results with those of patients who received usual care only.

Enrollment

45 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • A high risk of perioperative and postoperative complications. This risk is determined based on the predictive thresholds for postoperative complications.
  • A waiting period of at least 8 weeks.
  • Access to a smartphone, tablet, or computer for videoconference visits.

Exclusion criteria

  • Unstable angina, malignant arrhythmias, active endocarditis/myocarditis, myocardial infarction within the last 2 weeks, left main coronary artery disease ≥ 50% on coronary angiography, severe aortic stenosis, severe mitral insufficiency, and decompensated heart failure.
  • Any other acute condition affecting vital signs or causing significant symptoms.
  • Physical or cognitive impairment limiting the ability to participate in the program.

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

45 participants in 1 patient group

Prehab group
Experimental group
Description:
Supervised by a physiotherapist, the program includes an initial functional assessment, individualized training (breathing exercises, aerobic and strengthening exercises), and weekly follow-up via videoconference or phone.
Treatment:
Other: Exercise

Trial contacts and locations

1

Loading...

Central trial contact

Silvanna Cardoso

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems