we onderzoeken het welzijn van naasten van een patient die na de toepassing van continue sedatie is overleden
Conditions
Interventions
None listed
Sponsors
Erasmus MC, Universitair Medisch Centrum Rotterdam
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: The deceased patient: - Received continuous sedation until death - Cancer as main diagnosis - Older than 18 years of age - Passed away
Exclusion criteria
Exclusion criteria: Not fulfilling the inclusion criteria
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1) Focusgroup study It concerns a qualitative study. Therefore, there are no study parameters in the strict sense. In the focusgroups, the relatives will exchange their experiences with the care for the patient in the last phase of life. Relevant themes will be obtained from their narratives. 2) Interview study In the interviews, the following topics will be explored: - Patient characteristics - Relative characteristics - Decision-making and communication with the relative - The use of sedation - The patient's quality of dying - Wellbeing of the relative 3) Questionnaire study Primary study parameters are: satisfaction regarding the dying phase, concerns, grief and aspects of the quality of life after the patient's death (eg physical and mental functioning, role limitations). | — |
Secondary
| Measure | Time frame |
|---|---|
| 1) Focusgroup study Not applicable 2) Interview study Not applicable 3) Questionnaire study Secondary study parameters burned-out symptoms, sick-days | — |
Countries
Netherlands
Outcome results
None listed