Understanding the recovery of patients in rehabilitation after resuscitation
Characteristics and Evolution of Hospitalized Patients in Post-Resuscitation Rehabilitation Care Units (SRPR)
This study is tracking the recovery of patients in rehabilitation after being resuscitated to see how they improve over time and to help make rehab care better.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 1000 (estimated) |
| Sex | All |
| Sponsor | Assistance Publique - Hôpitaux de Paris Academic / other |
| Locations | 10 sites (Beaumont-sur-Oise and 9 other locations) |
| Trial ID | NCT03768700 on ClinicalTrials.gov |
What this trial studies
This observational cohort study aims to collect and analyze data from patients admitted to post-intensive care rehabilitation units in Ile de France and Rouen. It will track patients' progress through weekly follow-ups during their stay and at various intervals post-discharge, including 28 days, 90 days, and one year later. The study focuses on gathering comprehensive medical information, including ventilatory status and various health assessments, to predict patient outcomes and improve rehabilitation practices. By establishing criteria for patient selection, the research seeks to enhance the effectiveness of rehabilitation care.
Who should consider this trial
Good fit: Ideal candidates for this study are adults and children hospitalized in post-resuscitation rehabilitation care units in the specified regions.
Not a fit: Patients who refuse access to their medical data or those whose guardians do not consent will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved rehabilitation practices and better patient outcomes after resuscitation.
How similar studies have performed: While this approach is observational and focuses on data collection, similar studies have shown success in improving patient outcomes through data-driven insights.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Hospitalization in a Post-Resuscitation Rehabilitation Care Units (SRPR) of Ile de France and Rouen Exclusion Criteria: * Refusal of access to the data by the patient or the designated trusted person or the holder (s) of parental authority (pediatric population)
Where this trial is running
Beaumont-sur-Oise and 9 other locations
- Groupe hospitalier des portes de l'Oise — Beaumont-sur-Oise, France (Not_yet_recruiting)
- Centre hospitalier de Bligny — Briis-sous-Forges, France (Not_yet_recruiting)
- Hôpital d'instruction des armées - Percy — Clamart, France (Not_yet_recruiting)
- Hôpital de Forcilles — Férolles-Attilly, France (Not_yet_recruiting)
- Hôpital Raymond Poincaré - SRPR pédiatrique — Garches, France (Not_yet_recruiting)
- Hôpital Raymond Poincaré de Garches - SRPR neurologique — Garches, France (Not_yet_recruiting)
- Hôpital Bicêtre — Le Kremlin-Bicêtre, France (Not_yet_recruiting)
- Hôpital Pitié-Salpêtrière — Paris, France (Recruiting)
- Hôpital Sainte-Anne — Paris, France (Not_yet_recruiting)
- Hôpital Charles-Nicolle - CHU de Rouen — Rouen, France (Not_yet_recruiting)
Study contacts
- Principal investigator: Alexandre DEMOULE, Pr — Hôpital Pitié-Salpêtrière - AP-HP
- Study coordinator: Alexandre DEMOULE, Pr
- Email: alexandre.demoule@aphp.fr
- Phone: 0142167727
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.