About this trial
Prehab2Rehab is a prospective single-arm feasibility study evaluating the implementation of a multimodal, digitally supported prehabilitation program for adults awaiting elective cardiac surgery. During the routine preoperative waiting period, participants receive individualized education, psychosocial support, nutritional counselling, home-based physical activity guidance, and digital self-management support. The study aims to determine the feasibility, acceptability, usability, and safety of integrating this multidisciplinary prehabilitation pathway into routine clinical care. Exploratory outcomes include functional capacity, psychological well-being, nutritional status, digital engagement, and selected perioperative clinical outcomes to inform the design of future confirmatory trials.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Classification as New York Heart Association (NYHA) functional class I-II
Low surgical risk profile, defined as a EuroSCORE between 0 and 3
Open-heart valve surgery
Coronary artery bypass grafting (CABG)
Disqualifiers
Emergency, urgent, or otherwise non-elective cardiac surgery
Highly complex or specialized surgical procedures (e.g., aortic aneurysm repair, cardiac tumor resections)
Interventional cardiac procedures (e.g., transcatheter aortic valve implantation [TAVI], MitraClip interventions)
Neuromotor or physical impairments that might prevent adherence to the study protocol or informed participation
Trial design
Single group
Treatments tested in this trial
Digitally supported prehabilitation program
Other interventionThe Prehab2Rehab intervention is a personalized, multimodal, digitally supported prehabilitation program delivered during the routine 6-10 week preoperative waiting period before elective cardiac surgery. The program includes structured patient education, psychosocial support, nutritional assessment and counselling, individualized home-based physical activity guidance (including aerobic exercise, resistance training, breathing exercises, and inspiratory muscle training), and digital tools to support education, communication, self-management, and documentation. The intervention is delivered by a multidisciplinary team and complements routine perioperative care without altering standard clinical management.
Treatment groups
Trial outcomes
Primary outcomes
Proportion of eligible patients providing written informed consent (Recruitment rate)
Proportion of eligible patients who provide written informed consent and are enrolled in the study.
Proportion of enrolled participants completing the study (Participant retention)
Proportion of enrolled participants who complete the prehabilitation program and scheduled study assessments through follow-up.
Proportion of completed intervention components (Adherence to the prehabilitation program)
Participant adherence to the planned intervention components, including educational sessions, psychosocial support, nutritional counselling, home-based physical activity guidance, and use of digital support tools, assessed using attendance records and digital activity logs.
Proportion of completed study assessments and available study data (Data completeness)
Proportion of planned study assessments, questionnaires, and clinical data successfully completed at each scheduled assessment time point.
Sponsors and contacts
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Ludwig Boltzmann Institute for Digital Health and Prevention
Lead sponsor
Medical University of Vienna
Collaborator
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