The "Seamless" Patient:From Preoperative Preparation to Postoperative Rehabilitation
ConditionHeart Failure
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorHannover Medical School
About this trial
The "seamless" patient: from preoperative preparation to postoperative rehabilitation.
The effects of digital services for perioperative care of patients undergoing cardiac surgery will be investigated
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
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.
Disqualifiers
Emergency care;
congenital heart defects;
age less than 18 years;
patient unable to give consent;
Trial design
Design model
Parallel
Treatments tested in this trial
pre rehabilitation
Other interventionpreoperative pre-rehabilitation (respiratory training, exercise therapy). Establish an individualized rehabilitation plan and postoperative communication via telephone or app
Treatment groups
300 Participants
are divided into 3 treatment groupsGroup A: Standard of care"No intervention 0 interventions
Group B: Intensified patient educationOther 1 intervention
Group C: Intensified education on new media (mobile app)Other 1 intervention
Trial outcomes
Primary outcomes
1
Quality of life of patient via questionnaire
via questionnaire
Time frame
6 monthSponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov