From Prehabilitation to Rehabilitation (Prehab2Rehab): Digitally Supported Short-Term Prehabilitation Prior to Cardiac Surgery

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorLudwig Boltzmann Institute for Digital Health and Prevention

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 volunteers

Qualifiers

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

Design model

Single group

Treatments tested in this trial

  • Digitally supported prehabilitation program

    Other intervention

    The 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

40 Participants
are divided into 1 treatment group
Group A: Digitally Supported PrehabilitationExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

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.

Time frame
From study initiation until completion of recruitment (approximately 6 months)
2

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.

Time frame
From baseline until completion of follow-up after Phase II cardiac rehabilitation (approximately 4-6 months)
3

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.

Time frame
Throughout the preoperative intervention period (approximately 6-10 weeks)
4

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.

Time frame
From baseline until completion of follow-up after Phase II cardiac rehabilitation (approximately 4-6 months)

Secondary outcomes

Other outcomes

Sponsors and contacts

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