Percutaneous coronary intervention Bypass-OP I20.8
Conditions
Interventions
Group 1: Intervention 1. Goal setting at the end of rehabilitation.
Group 2: Intervention 2. Goal setting at the end of rehabilitation, in addition control-intervention three month after rehabilitaito
Sponsors
Charité - Universitätsmedizin Berlin, Lehrstuhl für Versorgungssystemforschung
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: After ACS, Bypass-OP, PCI.
Exclusion criteria
Exclusion criteria: Lack capacity to consent, lack of language skills.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change and continuity in the areas of physical activity, dietary habits, smoking, mental health, compliance to medication. Self-reported questionnaire at begin, end of rehabilitation and follow-up at 6 and 12 month after the end of rehabilitation. | — |
Secondary
| Measure | Time frame |
|---|---|
| Regulation of blood pressure, blood glucose, blood cholesteron. Collection of clinical parameters at begin and end of rehabilitation. Self-reported questionnaire at begin and end of rehabilitation as well as follow-up at 6 and 12 month after end of rehabilitation. | — |
Countries
Germany
Contacts
Public ContactSabine Stamm-Balderjahn
Charité - Universitätsmedizin Berlin, Lehrstuhl für Versorgungssystemforschung
Outcome results
None listed