Study in Intensive Care Follow-up Programme in Improving Long-term Outcomes of ICU Survivors

NACompletedINTERVENTIONAL
Enrollment

545

Participants

Timeline

Start Date

December 31, 2012

Primary Completion Date

September 30, 2018

Study Completion Date

March 11, 2020

Conditions
Quality of LifePost ICU Discharge
Interventions
OTHER

Medical, psychological, social

After having given his consent, the patient filled auto questionnaire, and then randomized either in follow up arm (i.e. intervention group) or in no follow up arm (i.e. control group). In the follow up arm, medical, psychological and social consultation will be planned within the first seven days after inclusion, and then 3, 6, 12 months. During medical consultation a general examination will be performed, muscle strength, cognitive function, functional disabilities will be assessed with help of MRC, MMS. During psychological consultation, anxiety and depression will be assessed with the help of HAD, IES. The psychologist will also have a free interview. During social consultation personal and professional reinsertion will be assessed.

Trial Locations (1)

92380

Hôpital Raymond Poincaré, Garches

All Listed Sponsors
lead

Assistance Publique - Hôpitaux de Paris

OTHER

NCT01796509 - Study in Intensive Care Follow-up Programme in Improving Long-term Outcomes of ICU Survivors | Biotech Hunter | Biotech Hunter