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Organ donation after controlled cardiac arrest: knowledge and acceptance among intensive care teams.

Organ donation after controlled cardiac arrest: knowledge and acceptance among intensive care teams. - DCD-ICU

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00039527
Enrollment
30
Registered
2026-03-11
Start date
2026-03-27
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Knowledge and attitudes toward organ donation after cardiac death

Interventions

Group 1: Qualitative, semi-structured individual interviews will be conducted online by video conference with nursing staff and physicians working in various German intensive care units.

Sponsors

Universitätsmedizin Greifswald
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: a) Belonging to one of the two study groups, “professional caregivers” or “physicians”: - A “professional caregiver” is defined here as a state-certified (3 years of training and/or study) nursing professional (nurse, healthcare and nursing professional, nursing specialist). - “Doctors” are defined here as assistant doctors in specialist training (rotational assistants), specialists (especially anesthesiologists), and (functional) senior physicians. b) Practical experience in the ICU: Both professional nurses and physicians should have at least 2 years of experience in direct patient care in an intensive care unit at the time of the interview. c) Practical experience with organ donation: Both professional nurses and physicians should have personal experience in accompanying potential organ donors at the time of the interview. d) Capacity for informed consent: A prerequisite for participation in both study groups is that the study participants consent to participate in the study after receiving verbal and written information (information sheet, consent form) and do not have any cognitive or linguistic deficits that would make informed consent or the conduct of the research interview impossible. However, it can be assumed that these requirements are met in the target group per se.

Exclusion criteria

Exclusion criteria: All persons who do not meet the above inclusion criteria

Design outcomes

Primary

MeasureTime frame
Data collection takes place once via an individual online interview. The interview questions focus on: - individual understanding of death and dying - personal experiences with organ donation - knowledge, understanding and acceptance of cDCD

Secondary

MeasureTime frame
not applicable.

Countries

Germany

Contacts

Public ContactAnna-Henrikje Seidlein

Universitätsmedizin Greifswad

Anna-Henrikje.Seidlein@med.uni-greifswald.de+4917632108910

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Apr 4, 2026