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

University Hospital Center (CHU) Dijon Bourgogne

Status: Enrolling

Conditions: Post Intensive Care Syndrome

Treatments: Other: Interdisciplinary consultation at 4/5 months; Other: Psychological and quality of life questionnaires

Study type: Interventional

Funder types: Other

Identifiers

NCT05625867

LAURENT UB 2022

Details and patient eligibility

About

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.

Enrollment: 404 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Person who has given oral consent
• Patient 18 years of age or older
• Patient with at least one organ failure
• Patient with a stay of 6 days or more

Exclusion criteria

• Person who is not affiliated or not a beneficiary of a social security system
• Patient at the end of his/her life
• Patient who does not speak French
• Minor (< 18 years old)
• Person subject to a legal protection measure (curatorship, guardianship)
• Person subject to a legal protection measure
• Pregnant, parturient or breastfeeding women
• Patient incarcerated
• Patient with a psychiatric history

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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404 participants in 2 patient groups

Post-resuscitation interdisciplinary consultation at 4/5 months after discharge from the ICU

Experimental group

Treatment:

Other: Psychological and quality of life questionnaires

Other: Interdisciplinary consultation at 4/5 months

Patient managed under standard practice conditions

Active Comparator group

Treatment:

Other: Psychological and quality of life questionnaires