Patients with heart disease and depressive symptoms I48 F32 I47 I49 F34 F43.2 F41.2 I20 I22 I23 I24 I25 I50
Conditions
Interventions
Group 1: The web-based intervention program weekly schedules modules that are based on cognitive-behavioral methods. Each module requires about one hour to complete. A video moderation leads through t
Sponsors
AG Klinische Neuropsychologie, Klinik für Psychiatrie und Psychotherapie Universitätsklinikum Hamburg-Eppendorf
Eligibility
Sex/Gender
All
Age
18 Years to 85 Years
Inclusion criteria
Inclusion criteria: Written informed consent , Depressive symptoms, heart disease
Exclusion criteria
Exclusion criteria: lifetime history of bipolar disorder or schizophrenia, Presence of dementia (for example Alzheimer's disease), acute suicidal tendencies
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Beck Depression Inventory II (BDI-II); two assessments (pre-post), 12 weeks intervention period | — |
Secondary
| Measure | Time frame |
|---|---|
| pre: sociodemographic questionnaire pre und post: Beck Depression Inventory (BDI-II) SF-12 Health Survey (State) Trait Anxiety Inventory (STAI) Minnesota Living with Heart Failure Questionnaire (MLHFQ) Medication Adherence Report Scale (MARS-D) Freiburg Questionnaire on Coping with Illness (FQCI) Attitudes towards Psychological Online Interventions Questionaire (APOI) Blood pressure and pulse rate blood count blood lipids HbA1C post: Client Satisfaction Questionnaire (CSQ-8) Compliance questionnaire Inventory for the Assessment of Side Effects | — |
Countries
Germany
Contacts
Public ContactJohanna schröder
AG Klinische Neuropsychologie,Klinik für Psychiatrie und Psychotherapie Universitätsklinikum Hamburg-Eppendorf
Outcome results
None listed