Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Improving care for heart surgery patients through digital services

Official title: The "Seamless" Patient: From Preoperative Preparation to Postoperative Rehabilitation

Run by Hannover Medical School · NCT06699446 · Data updated 2026-11-12

This study is testing whether using a mobile app for communication and support can help heart surgery patients recover better compared to standard care or traditional education methods.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment300 (estimated)
SponsorHannover Medical School
Academic / other
Locations1 site (Hanover, Lower Saxony)
StatusRecruiting
StartedJune 28, 2023
Main results expectedJune 2026
Study endsDecember 2026
Registry record updatedNovember 21, 2024
Trial IDNCT06699446 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults scheduled for elective cardiac surgery, such as coronary bypass or heart valve surgery.

Probably not a fit

Patients requiring emergency surgery or those with congenital heart defects may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study investigates the effects of digital services on perioperative care for patients undergoing cardiac surgery. Participants will be randomized into three groups: one receiving standard care, another receiving intensified education through traditional methods, and a third utilizing a mobile app for enhanced communication and rehabilitation. The goal is to establish individualized rehabilitation plans and improve patient-reported outcomes through better information exchange and support. By integrating digital tools, the study aims to enhance the quality of life and reduce postoperative complications.

Why it matters

Potential benefit: If successful, this approach could significantly improve recovery outcomes and quality of life for heart surgery patients.

How similar studies have gone: Other studies have shown promise in using digital tools for patient care, suggesting potential success for this approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patient is capable of giving consent;
* planned, elective cardiac surgery (coronary bypass surgery and heart valve surgery incl. combination surgery). The planned surgery can be performed with or without a heart-lung machine.
* Minimally invasive procedures may also be explicitly included in the study.

Exclusion Criteria:

* Emergency care;
* congenital heart defects;
* age less than 18 years;
* patient unable to give consent;
* patient unable to perform simple physical training;
* high-risk surgery with a calculated Euroscore II of more than 8%.

Where it's running

  • Medical School Hanover
    Hanover, Lower Saxony, Germany
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.