Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05625867

Post-Resuscitation Interdisciplinary Consultation System: a Randomized, Multicenter, Interventional Study to Assess Quality of Life After a Stay in the COPRéa Intensive Care Unit

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
404 (estimated)
Sponsor
Centre Hospitalier Universitaire Dijon · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

A patient's stay in the ICU is not without consequences and can cause various physical and/or psychological sequelae such as anxiety, depression, post-traumatic stress disorder (PTSD), physical weakness and memory problems. These sequelae are grouped under the name "post intensive care syndrome" or PICS. Numerous studies have shown that PICS affects 50-70% of patients; however, very few studies have been conducted on the medical and psychological support devices needed for these patients following their hospitalization. Despite recommendations to set up an early and specific rehabilitation program, post-resuscitation consultations are not very frequent in France. The aim of the study is to measure the impact of an interdisciplinary post-resuscitation consultation on the quality of life of patients who have stayed more than 6 days in an intensive care unit. All patients who agreed to participate will be followed for a period of 9 months after discharge from the ICU. One month after discharge from the ICU, the patients will be randomly assigned to * either in the "intervention" group who will benefit from an interdisciplinary post resuscitation consultation 4/5 months after their discharge from the intensive care unit * or in the "control" group without post resuscitation consultation. They will all be contacted at 4/5 and 9 months to complete psychological and quality of life questionnaires.

Conditions

Interventions

TypeNameDescription
OTHERPsychological and quality of life questionnairesAt 4/5 months and at 9 months
OTHERInterdisciplinary consultation at 4/5 monthsAbout ten days after the questionnaires were administered

Timeline

Start date
2023-02-05
Primary completion
2026-05-01
Completion
2026-05-01
First posted
2022-11-23
Last updated
2024-11-05

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT05625867. Inclusion in this directory is not an endorsement.