MedTrace Logo

The PREBEAT Trial: Digital PREhaBilitation in thE Cardiac Surgical populATion

NCT06983808 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2025-06-06

No results posted yet for this study

Summary

The goal of this randomised controlled trial is to learn if a digital prehabilitation program is feasible in patients awaiting cardiac surgery. The main questions it aims to answer are:

1. Is the digital health program usable?
2. Is the digital health program acceptable?
3. Do patients adhere to the digital health program?

Researchers will compare a group using the digital prehabilitation program with standard care to see if the program is feasible and explore any differences in health outcomes.

Participants will

* Use a digital health mobile phone application to guide you through exercise, nutrition and preparation for surgery.
* Engage in telehealth consultations.
* Complete questionnaires
* Complete exercise testing

Conditions

Interventions

OTHER

Digital Cardiac Prehabilitation

Digital Cardiac Prehabilitation - A combined telehealth and app-based preparation for cardiac surgery

OTHER

Control (Standard treatment)

Standard preparation for surgery as per Melbourne Health hospital procedures and processes. This may include information sessions, pamphlets, and meetings with clinicians. This does not include a prehabilitation program.

Sponsors & Collaborators

  • Melbourne Health

    collaborator OTHER

  • Claire Hines

    lead OTHER

Principal Investigators

  • Alistair Royse, MD - Cardiothoracic Surgeon · Melbourne Health

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-07-01
Primary Completion
2026-03-31
Completion
2026-12-31

Countries

  • Australia

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06983808 on ClinicalTrials.gov