Improving quality of life for ICU patients after discharge
Post-Resuscitation Interdisciplinary Consultation System: a Randomized, Multicenter, Interventional Study to Assess Quality of Life After a Stay in the COPRéa Intensive Care Unit
This study tests if a new support system can help ICU patients feel better and improve their quality of life after they leave the hospital.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 404 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Centre Hospitalier Universitaire Dijon Academic / other |
| Locations | 1 site (Dijon) |
| Trial ID | NCT05625867 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of an interdisciplinary consultation system aimed at improving the quality of life for patients who have experienced post-intensive care syndrome (PICS) after a stay in the ICU. Participants will undergo psychological assessments and receive consultations four to five months post-discharge to address the physical and psychological sequelae associated with their ICU stay. The study will follow patients for nine months to measure the impact of these interventions on their recovery and overall well-being.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older who have experienced at least one organ failure and have been hospitalized in the ICU for six days or more.
Not a fit: Patients who are at the end of life, do not speak French, or have significant psychiatric histories may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly enhance the quality of life for ICU survivors by providing targeted support for PICS.
How similar studies have performed: While many studies have identified the prevalence of PICS, few have tested structured post-resuscitation support systems, making this approach relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
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
Where this trial is running
Dijon
- Chu Dijon Bourgogne — Dijon, France (Recruiting)
Study contacts
- Study coordinator: Alexandra LAURENT
- Email: alexandra.laurent@u-bourgogne.fr
- Phone: 03 80 39 39 77
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.