DEVELOPMENT AND PILOTING OF AN ONLINE-BASED INTERVENTION FOR ONCOLOGICAL STAFF TO PROMOTE MENTAL HEALTH
- Conditions
- Compassion SatisfactionDepression, anxiety, burnout, resilience, workability,
- Registration Number
- DRKS00018851
- Lead Sponsor
- niversitätsklinikum Heidelberg
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 120
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.
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.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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 Outcome Measures
Name Time Method 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.