Trials / Completed
CompletedNCT05817500
Post-ICU Consultation : a Time to Discuss Advance Directives (CoPRADA)
Post-ICU Consultation : a Time to Discuss Advance Directives
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 40 (actual)
- Sponsor
- University Hospital, Brest · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The aim of this study is to assess the possibility of discussing advance directives during post-intensive care consultation.
Detailed description
After a stay in intensive care units (ICU), patients can experience physical, psychological and cognitive impairments. To assess this post intensive care syndrom (PICS), post-ICU consultation have been developed. Since 5 year mortality is higher in ICU survivors, it might be interesting to address those patients' views relating to illness and end of life through a discussion on advance directives (AD), during post-ICU consultation. However, the development of these consultations being recent, it has not yet been assessed whether this consultations might be a suitable time to discuss AD and the intensivit a suitable interlocutor.
Conditions
Timeline
- Start date
- 2021-12-09
- Primary completion
- 2022-12-09
- Completion
- 2022-12-09
- First posted
- 2023-04-18
- Last updated
- 2023-04-18
Locations
1 site across 1 country: France
Source: ClinicalTrials.gov record NCT05817500. Inclusion in this directory is not an endorsement.