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Effect of the use of continuous sedation until death on the patient's relatives wellbeing

Effect of the use of continuous sedation until death on the patient's relatives wellbeing - UNBIASED

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON38210
Enrollment
625
Registered
2011-01-21
Start date
2011-03-15
Completion date
Unknown
Last updated
2024-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

we onderzoeken het welzijn van naasten van een patient die na de toepassing van continue sedatie is overleden

Interventions

None listed

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

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

MeasureTime 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

MeasureTime 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

Source: NL-OMON (via WHO ICTRP)