Clinical Trials Directory

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.