Clinical Trials Logo

Clinical Trial Summary

Sudden death is a public health problem with more than 300,000 cases per year in USA and 40,000 cases per year in France. Moreover, despite all recent therapeutic improvements (therapeutic hypothermia, new techniques of resuscitation…), the prognosis remains drastically poor and less than 50% of the patients admitted alive at hospital will survive to the event at 1 year.

Outside all medications and technical care to improve patient prognosis, a psychological evaluation looks also critical to detect the occurrence of a "post traumatic stress syndrome". In fact, along with the event severity, a variable period of amnesia related to coma may favor the occurrence of such a syndrome and psychological issues, which at the end may lead to impairment of patient quality of life.

Previous studies have evaluated the impact of an intensive care unit diary on psychological distress in patients and relatives in the context of severe traumatisms. Such an evaluation has however never been done in the specific setting of sudden death and the frequency of this syndrome is unknown in this context.

Aim The aim of the present study is to evaluate the impact of an intensive care unit diary on the occurrence of a "post traumatic stress syndrome" after a sudden death.

Secondary objectives

- To evaluate the frequency of the occurrence of a "post traumatic stress syndrome" and other psycho traumatic symptoms after sudden death

- To evaluate the impact of an intensive care unit diary on the severity of this syndrome, psycho traumatic symptoms, and psychopathologic comorbidities

- To evaluate the impact of the diary on psycho traumatic symptoms and their severity in patient's relatives

- To evaluate the satisfaction of the patients and their relatives regarding medical cares in both groups (with and without diary)

- Comparison of nurse diagnostic (psychological distress) and diagnostic made by dedicated personal with a specific formation in psychology

- Qualitative evaluation of the diary

- Evaluation of the paramedical feeling before and after the diary input in practice


Clinical Trial Description

The COREABOR Study is an open label, prospective, that will compare patients with sudden death who will be included during 2 successive periods of time: first a period of control and then a period of intervention.

Interventional study.

Altogether, 330 patients with resuscitated sudden death will be screened during the whole study period allowing to include 96 patients in the study (alive at 3 months after the event, estimated survival rate of 30%). For each screened patient, 2 relatives will be selected to participate to the study (n=660).

To avoid biases, the control group of 48 patients will be included first and treated as recommended with usual care in center. Then, the 48 patients of the intervention group will be included during the second period of the study and the intensive care unit diary will be implemented only at this time.

In the intervention group (second period with diary), a maximal delay of 8 hours is allowed to implement the diary for each patient after admission in centre.

Visit 0 (V0): inclusion The study will recruit patients in the total incapacity to give their own consent for medical reasons (comatose patients) at admission. Subsequently a written inform consent of a relative will first be obtained and the patient's written consent will be obtained as soon as possible afterwards.

Period 1: control group Medical care as usually performed in center and as recommended.

Period 2: intervention group (intensive care unit diary) On top of usual care, an intensive care unit diary will be implemented for all patients within the first 8 hours following their admission. At discharge, the diary will be given to the patients themselves or to their relatives in case of in-hospital death. An anonymous copy will be kept by investigators.

For all patients A psychological evaluation will be performed at 1 month (V1), 3 months (V2) and 6 months by phone contact only (V3) using the following elements Auto-questioner (PDI) Nurse diagnosis Psychological evaluation by dedicated personal (CAPS and mini-DSMIV)

For relatives A psychological evaluation will be performed at 3 months (V2) and 6 months by phone contact only (V3) ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02874469
Study type Interventional
Source University Hospital, Lille
Contact Hélène Dehaut
Email lndehaut@gmail.com
Status Recruiting
Phase N/A
Start date December 31, 2014
Completion date November 2023

See also
  Status Clinical Trial Phase
Completed NCT00226681 - Nurses Helping Sudden Cardiac Arrest Survivors Recover After Getting An Implantable Cardioverter Defibrillator (ICD) Phase 1
Recruiting NCT05799833 - Low QRS Voltages in Young Healthy Individuals and Athletes
Completed NCT05636332 - The Intrepid Clinical Engineering Study N/A
Recruiting NCT04250857 - HeartStart FRx Defibrillator Event Registry
Recruiting NCT02816047 - Austrian Wearable Cardioverter Defibrillator Registry
Completed NCT00918125 - Educational Videos to Improve Patient Decision Making and Race Disparities in Implantable Cardioverter Defibrillator Use N/A
Recruiting NCT05135403 - ASSURE WCD Clinical Evaluation - Post Approval Study (ACE-PAS)
Completed NCT03715790 - Improve SCA Bridge Study
Recruiting NCT03826524 - Epinephrine Dose: Optimal Versus Standard Evaluation Trial Phase 4
Recruiting NCT05855135 - Assessment of Combined CCM and ICD Device in HFrEF N/A
Completed NCT03065647 - ECPR for Refractory Out-Of-Hospital Cardiac Arrest N/A
Completed NCT02099721 - Improve Sudden Cardiac Arrest Study N/A
Recruiting NCT01822145 - A Feasibility Study on Prediction of an ICD Shock by ICD-derived Data N/A
Completed NCT01326624 - Study of the Wearable Defibrillator in Heart-Failure Patients N/A
Completed NCT03016754 - Heart Failure Optimization Study
Terminated NCT02481206 - Wearable Cardioverter Defibrillator in Hemodialysis Patients (WED-HED) Study N/A
Enrolling by invitation NCT04548804 - Better Mechanistic Understanding of and Risk Stratification for Ventricular Tachyarrhythmias Through ECGI N/A
Enrolling by invitation NCT05490459 - Jewel Electrophysiology (EP) Lab Study N/A
Recruiting NCT01521208 - LUCAS Chest Compressor Versus Manual Chest Compression in Out-of-hospital Sudden Cardiac Arrest. LUCAT Trial Phase 3
Completed NCT05201495 - The Jewel IDE Study N/A