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Impact of an Intensive Care Diary on Post-traumatic Stress Disorder After a Resuscitated Sudden Death (COREABOR)

Primary Purpose

Sudden Death, Sudden Cardiac Arrest

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Diary
Sponsored by
University Hospital, Lille
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Sudden Death focused on measuring sudden death, post-traumatic stress disorder, psychological distress, diary, resuscitation

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria =

  • Patients who experienced a sudden death and who are admitted alive in our center
  • Patients who benefited from therapeutic hypothermia (and/or care to limit fever occurrence)

Relative's inclusion criteria :

  • Relatives of a patient that fit inclusion/exclusion criteria

Exclusion Criteria =

Patient's non-inclusion criteria :

  • Death or transfer in another center within the first 8 hours of admission in our center
  • Pregnancy
  • Patients who refuse to participate after being awake after initial coma

Relative's non-inclusion criteria :

  • Relatives who refuse to participate after being awake after initial coma

Sites / Locations

  • Hôpital Cardiologique - USIC - CHRURecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Control group (first period)

Group with diary (second period)

Arm Description

Patients treated as recommended with usual care in a center.

Intervention group = On top of usual care, an intensive care unit diary will be implemented for patients within the first 8 hours following their admission.

Outcomes

Primary Outcome Measures

Rate of occurrence of "post traumatic stress disorder"
Rate of occurrence of "post traumatic stress syndrome" (CAPS score over 39) at 3 months after resuscitation after sudden death

Secondary Outcome Measures

Peritraumatic Distress Inventory (PDI) Scale
PDI is a scale of self-evaluation of 13 items to determine distress reactions emotional of a person at the time of a traumatic event and in the minutes and hours. People who have a high risk of distress Peritraumatic develop post-traumatic stress disorder.
Psychiatric comorbidities
Psychiatric comorbidities evaluated by the mini DSM IV (Diagnostic and Statistical Manual of Mental Disorders - IV) for patients
Rate of "Post traumatic stress disorder" for patients
Rate of "Post traumatic stress disorder" (CAPS score over 39) for patients
Rate of "Post traumatic stress disorder" for relatives
Rate of "Post traumatic stress disorder" (CAPS score over 39) for relatives
Nurse diagnosis
Comparison of nurse diagnosis and diagnosis made by dedicated personal with a specific formation in psychology
Qualitative evaluation of the diary
Qualitative evaluation of the diary by satisfaction questionnaire

Full Information

First Posted
August 17, 2016
Last Updated
August 26, 2020
Sponsor
University Hospital, Lille
Collaborators
Ministry of Health, France
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1. Study Identification

Unique Protocol Identification Number
NCT02874469
Brief Title
Impact of an Intensive Care Diary on Post-traumatic Stress Disorder After a Resuscitated Sudden Death
Acronym
COREABOR
Official Title
Impact of an Intensive Care Diary on Post-traumatic Stress Disorder on Patients After a Resuscitated Sudden Death and His Relatives
Study Type
Interventional

2. Study Status

Record Verification Date
August 2020
Overall Recruitment Status
Recruiting
Study Start Date
December 31, 2014 (Actual)
Primary Completion Date
November 2023 (Anticipated)
Study Completion Date
November 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Lille
Collaborators
Ministry of Health, France

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief 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
Detailed 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)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sudden Death, Sudden Cardiac Arrest
Keywords
sudden death, post-traumatic stress disorder, psychological distress, diary, resuscitation

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
330 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control group (first period)
Arm Type
No Intervention
Arm Description
Patients treated as recommended with usual care in a center.
Arm Title
Group with diary (second period)
Arm Type
Experimental
Arm Description
Intervention group = On top of usual care, an intensive care unit diary will be implemented for patients within the first 8 hours following their admission.
Intervention Type
Other
Intervention Name(s)
Diary
Intervention Description
The diary was specifically created for the purpose of the present study by personal working at ICU at CHRU of Lille (France). All relatives, doctors and paramedics close to the patient during his hospital stay are allowed to write some comments inside the diary when he is comatose. The diary will be implemented during the second period of the study within the first 8 hours after admission. It will be given to the patients themselves at discharge or to their relatives in case of in-hospital death. An anonymous copy will be kept by investigators.
Primary Outcome Measure Information:
Title
Rate of occurrence of "post traumatic stress disorder"
Description
Rate of occurrence of "post traumatic stress syndrome" (CAPS score over 39) at 3 months after resuscitation after sudden death
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Peritraumatic Distress Inventory (PDI) Scale
Description
PDI is a scale of self-evaluation of 13 items to determine distress reactions emotional of a person at the time of a traumatic event and in the minutes and hours. People who have a high risk of distress Peritraumatic develop post-traumatic stress disorder.
Time Frame
1 month
Title
Psychiatric comorbidities
Description
Psychiatric comorbidities evaluated by the mini DSM IV (Diagnostic and Statistical Manual of Mental Disorders - IV) for patients
Time Frame
3 and 6 months
Title
Rate of "Post traumatic stress disorder" for patients
Description
Rate of "Post traumatic stress disorder" (CAPS score over 39) for patients
Time Frame
6 months
Title
Rate of "Post traumatic stress disorder" for relatives
Description
Rate of "Post traumatic stress disorder" (CAPS score over 39) for relatives
Time Frame
3 and 6 months
Title
Nurse diagnosis
Description
Comparison of nurse diagnosis and diagnosis made by dedicated personal with a specific formation in psychology
Time Frame
3 months
Title
Qualitative evaluation of the diary
Description
Qualitative evaluation of the diary by satisfaction questionnaire
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria = Patients who experienced a sudden death and who are admitted alive in our center Patients who benefited from therapeutic hypothermia (and/or care to limit fever occurrence) Relative's inclusion criteria : Relatives of a patient that fit inclusion/exclusion criteria Exclusion Criteria = Patient's non-inclusion criteria : Death or transfer in another center within the first 8 hours of admission in our center Pregnancy Patients who refuse to participate after being awake after initial coma Relative's non-inclusion criteria : Relatives who refuse to participate after being awake after initial coma
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Hélène Dehaut
Email
lndehaut@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gilles LESMESLE, MD, PhD
Organizational Affiliation
University Hospital, Lille
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hôpital Cardiologique - USIC - CHRU
City
Lille
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hélène Dehaut
Email
lndehaut@gmail.com
First Name & Middle Initial & Last Name & Degree
Gilles Lemesle
Email
gilles.lemesle@chru-lille.fr
First Name & Middle Initial & Last Name & Degree
Gilles Lemesle, MD,PhD

12. IPD Sharing Statement

Plan to Share IPD
No

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Impact of an Intensive Care Diary on Post-traumatic Stress Disorder After a Resuscitated Sudden Death

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