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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorCentre Hospitalier Universitaire Dijon

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

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)

Trial design

Design model

Parallel

Treatments tested in this trial

  • Psychological and quality of life questionnaires

    Other intervention

    At 4/5 months and at 9 months

  • Interdisciplinary consultation at 4/5 months

    Other intervention

    About ten days after the questionnaires were administered

Treatment groups

404 Participants
are divided into 2 treatment groups
Group A: Post-resuscitation interdisciplinary consultation at 4/5 months after discharge from the ICUExperimental treatment 2 interventions
Group B: Patient managed under standard practice conditionsActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

MOS SF-36 Quality of Life Scale Score

Time frame
Between 4/5 and 9 months after discharge from intensive care

Secondary outcomes

Other outcomes

Sponsors and contacts

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