Proactive Communication Strategy in Intensive Care Unit and Post Traumatic Stress Symptoms (FAMIREAXV)
Primary Purpose
Critically Ill Patients
Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
End of ICU stay conference
Sponsored by
About this trial
This is an interventional prevention trial for Critically Ill Patients focused on measuring ICU, Anxiety, Depression, PTSD
Eligibility Criteria
Inclusion Criteria:
- patient alive at the end of ICU stay
- age > 18 years
- more than 48 hours of mechanical ventilation
- accepting to be called back 3-month and on one year after discharge of ICU.
Exclusion Criteria:
- chronic cognitive deterioration before ICU admission
- inclusion in another interventional randomized essay
- non French-speaking patients
- impossibility to agree for participation
- end of life situation (survival at 3 months very improbable)
- deaf-dumb patients.
Sites / Locations
- Medical ICU
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
End of ICU stay conference
Usual Procedure
Arm Description
Conference with patient and proxies, senior physician and nurse regarding the ICU stay and the orientation of the patient
Usual discharge procedure from the ICU
Outcomes
Primary Outcome Measures
Symptoms of PTSD in ICU patients
Secondary Outcome Measures
Symptoms of PTSD, anxiety, and depression in ICU patients
Symptoms of PTSD, anxiety, and depression in ICU patients
Symptoms of PTSD, anxiety, and depression in families
Symptoms of PTSD, anxiety, and depression in families
Full Information
NCT ID
NCT01147978
First Posted
June 18, 2010
Last Updated
April 22, 2014
Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
University Paris 7 - Denis Diderot, Institut National de la Santé Et de la Recherche Médicale, France
1. Study Identification
Unique Protocol Identification Number
NCT01147978
Brief Title
Proactive Communication Strategy in Intensive Care Unit and Post Traumatic Stress Symptoms
Acronym
FAMIREAXV
Official Title
Impact of a Proactive Strategy of Communication With Patients Hospitalized in ICU and Their Families With the Aim of Reducing Their Anxious and Depressive Symptoms and Their Post Traumatic Stress Symptoms
Study Type
Interventional
2. Study Status
Record Verification Date
April 2014
Overall Recruitment Status
Completed
Study Start Date
April 2009 (undefined)
Primary Completion Date
August 2012 (Actual)
Study Completion Date
November 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
University Paris 7 - Denis Diderot, Institut National de la Santé Et de la Recherche Médicale, France
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The investigators propose an interventional multicentric (23 ICUs) study measuring the impact of a consultation at the end of ICU stay for the patients and his/her families on the prevalence of symptoms of PTSD and anxiety or depression 3 months and one year after discharge. Patients will be randomly assigned to a intervention or control group. In the intervention group, the patient and his/her family will benefit from an conference by the intensivist at the end of the ICU stay, regarding information about the progress of his stay in ICU, his orientation after discharge, the possibility of consulting a GP, etc. Patients and proxies will be interviewed by phone three months and one year after discharge from ICU. Main instruments are Hospital Anxiety and Depression Scale, and Impact of Events Scale Revised.
Detailed Description
There are many risk factors of stress for a patient during a stay in Intensive care unit. This stress can be responsible for psychiatric symptoms hindering seriously the quality of life of the patient in the months following discharge from ICU. Survivors of ICU suffer from traumatic memories (nightmares, acute anxiety), who can be associated to post traumatic stress disorder (PTSD) or of anxious and depressive symptoms. Prevalence of PTSD in the months following ICU stay is estimated between 14 and 41 %, that of the symptoms of anxiety between 12 % and 47 %, and that of the symptoms of depression between 10 % and 30 %. Recent studies showed that these symptoms could concern several thousand patients every year in France.
We propose an interventional multicentric (23 ICUs) study measuring the impact of a consultation at the end of ICU stay for the patients and his/her families on the prevalence of symptoms of PTSD and anxiety or depression 3 months and one year after discharge.
Patients will be randomly assigned to a intervention or control group. In the intervention group, the patient and his/her family will benefit from an conference by the intensivist at the end of the ICU stay, regarding information about the progress of his stay in ICU, his orientation after discharge, the possibility of consulting a general practitioner (GP), etc. The family, if present, will be invited to attend the conference. In the control group, patients will be cared in a usual way (without end of stay conference) as it is made in all the intensive care units in France. Inclusion criteria are 1) patient alive at the end of ICU stay, 2) Age > 18 years, 3) more than 48 hours of mechanical ventilation 4) accepting to be called back 3-month and on one year after discharge of ICU. Exclusion criteria are 1) Chronic cognitive deterioration before ICU admission, 2) inclusion in another interventional randomized essay 3) non French-speaking patients, 4) impossibility to agree 5) End of life situation (survival at 3 months very improbable), 6) deaf-dumb patients. Patients and proxies will be interviewed by phone three months and one year after discharge from ICU. Main instruments are Hospital Anxiety and Depression Scale, and Impact of Events Scale Revised. Number of patients to include takes into account an estimated prevalence of PTSD of 20 %, and the impact expected from the intervention is to obtain 10 % of PTSD in the intervention group. With a beta power of 90 % and a risk of 5 %, number of patients needed three months after discharge is 438 (219 in every group), i.e 525 patients (263 in every arm because of the late deaths and lost sight). This study should supply updated and relevant data on prevalence and risk factors of symptoms of PTSD and Anxiety-depression three months and one year after discharge from ICU. Furthermore, we propose an intervention that could demonstrate that a brief and easily reproducible communication strategy could significantly reduce prevalence of PTSD and anxiety-depression for patients and their families after discharge from ICU
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Critically Ill Patients
Keywords
ICU, Anxiety, Depression, PTSD
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
303 (Actual)
8. Arms, Groups, and Interventions
Arm Title
End of ICU stay conference
Arm Type
Experimental
Arm Description
Conference with patient and proxies, senior physician and nurse regarding the ICU stay and the orientation of the patient
Arm Title
Usual Procedure
Arm Type
No Intervention
Arm Description
Usual discharge procedure from the ICU
Intervention Type
Behavioral
Intervention Name(s)
End of ICU stay conference
Intervention Description
Conference with patient and proxies, senior physician and nurse regarding the ICU stay and the orientation of the patient
Primary Outcome Measure Information:
Title
Symptoms of PTSD in ICU patients
Time Frame
three months after discharge from ICU
Secondary Outcome Measure Information:
Title
Symptoms of PTSD, anxiety, and depression in ICU patients
Time Frame
three months after discharge from ICU
Title
Symptoms of PTSD, anxiety, and depression in ICU patients
Time Frame
one year after discharge from ICU
Title
Symptoms of PTSD, anxiety, and depression in families
Time Frame
three months after discharge from ICU
Title
Symptoms of PTSD, anxiety, and depression in families
Time Frame
one year after discharge from ICU
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
patient alive at the end of ICU stay
age > 18 years
more than 48 hours of mechanical ventilation
accepting to be called back 3-month and on one year after discharge of ICU.
Exclusion Criteria:
chronic cognitive deterioration before ICU admission
inclusion in another interventional randomized essay
non French-speaking patients
impossibility to agree for participation
end of life situation (survival at 3 months very improbable)
deaf-dumb patients.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Elie AZOULAY, MD PhD
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
Medical ICU
City
Paris
ZIP/Postal Code
75010
Country
France
12. IPD Sharing Statement
Learn more about this trial
Proactive Communication Strategy in Intensive Care Unit and Post Traumatic Stress Symptoms
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