Compassion Satisfaction Depression, anxiety, burnout, resilience, workability,
Conditions
Interventions
Group 1: After inclusion of the test persons, an explanatory discussion takes place in which the intervention is presented and its treatment explained. This is followed by a qualitative and quantitati
Sponsors
Universitätsklinikum Heidelberg
Eligibility
Sex/Gender
All
Age
18 Years to 100 Years
Inclusion criteria
Inclusion criteria: Participation requires cooperation in oncology as a nurse or physician. The study participants must be 18 years of age or older, have access to a smartphone or the Internet, have German as their mother tongue or very good German language skills, and have the technical prerequisites for carrying out the intervention. All persons who agree to participate in the study will receive the information leaflet and the declaration of consent, which will also be explained orally. The participation in the study requires the receipt of a written consent documented by a signature or, in the case of an online survey, confirmation of the consent by clicking on the corresponding button.
Exclusion criteria
Exclusion criteria: Not included in the study are participants with cognitive or physical impairments that complicate online program processing, severe mental illness, age < 18 years, and lack of written consent to participate.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| As soon as all n=20 study participants have completed the online training (pilot study), the data collection will be completed. If this is not achieved within one year after the start of the study, the study will be completed with the number of participants available at that time. The quantitative survey is carried out online and comprises the following validated questionnaires: Workability Index (Hasselhorn & Freude, 2007), PHQ-4 (Löwe et al., 2010), Oldenburger Burnout Invententar (Demerouti & Bakker, 2008), the scales `Compassion Satis-faction´ and `secondary traumatic Stress´ from the Proqol-5 (Stamm, 2010) as well as the resilience scale RS-13 (Leppert, Koch, Brähler & Strauß, 2008). | — |
Secondary
| Measure | Time frame |
|---|---|
| Revocation of the participant's consent to study participation, whereby the participant's consent to study participation may be revoked at any time and without giving reasons. | — |
Countries
Germany
Contacts
Public ContactMadeleine Helaß
Universitätsklinikum Heidelberg Klinik für Allgemeine Innere Medizin und Psychosomatik II
Outcome results
None listed