Feasibility and acceptance of an internet-based preoperative intervention optimizing patients’ expectations to improve outcome in heart surgery patients (the iHEART trial)
Not Applicable
- Conditions
- I25Chronic ischaemic heart disease
- Registration Number
- DRKS00033284
- Lead Sponsor
- Philipps-Universität Marburg
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 160
Inclusion Criteria
Medical necessity to perform a CABG, median sternotomy, sufficient knowledge of the German language, Adequate cognitive fitness to give consent to participate in the study, Valid email address, Regular access to a computer with an internet connection, At least 5 to 21 days before the surgery.
Exclusion Criteria
Presence of a life-threatening comorbid physical illness; presence of another medical condition that affects quality of life more than the heart disease, or presence of an acute psychiatric disorder
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method