Feeling of loss of control
Conditions
Interventions
Group 1: Resulting from the data analysis of first project steps (test battery of questionnaires and interviews), an intervention will be developed at the end of the project time. Feasibility and burd
Sponsors
Klinik für Palliativmedizin
Universitätsklinikum
RWTH Aachen
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. relevant palliative care treatment setting 2. all patients within a 12 month evaluation period 3. sufficient general condition for quantitative evaluation of test battery (and additional interview) 4. informed consent for study participation (and interview recording)
Exclusion criteria
Exclusion criteria: 1. missing informed consent 2. insufficient general condition for quantitative evaluation of test battery (and additional interview)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Description of self-efficiacy beliefs and locus of control of patients receiving palliative care from questionnaires and their subjective perception of loss of control from the interviews; Development, test and evaluation of an intervention pro feeling of control | — |
Secondary
| Measure | Time frame |
|---|---|
| Registering a statement concerning a feeling of loss of control, the patient will be included in an intevention (informed consent). The interventionw ill be analysed regarding feasibility and burden for the patient. A post conversation 2-4 days after the intervention, changes in emotions and cognition will be questioned. | — |
Countries
Germany
Contacts
Public ContactStephanie Stiel
Klinik für Palliativmedizin Universitätsklinikum RWTH Aachen
Outcome results
None listed