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Near-death Experience in ICU Survivors

Completed
Conditions
Critical Illness
Near-Death Experience
Registration Number
NCT04279171
Lead Sponsor
University of Liege
Brief Summary

This observational study aims to describe the incidence of near-death experience (NDE) in patients who survived a critical illness. In order to help determine the potential risk factors of NDE, dissociative status and spirituality are also investigated. Finally, in patients who experienced NDE, a magnetic resonance imaging is performed to search for any structural modifications.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
126
Inclusion Criteria
  • All consecutive patients who survived critical illness
Exclusion Criteria
  • Glasgow Coma Scale < 15/15
  • Confusion (CAM ICU scale)
  • Refusal

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
NDEGreyson questionnaire is administered during the week following ICU discharge

NDE occurence during ICU stay, retrospectively detected by the Greyson scale. Greyson scale is a 16 items and 32 points scale. Minimal score is 0, maximal score is 32. A NDE is suspected when score is equal or higher than 7.

Secondary Outcome Measures
NameTimeMethod
Quality of life estimationone year after first interview

Quality of life assessment, using EQ-5D-3L

NDEone year after first interview

NDE occurence during ICU stay, retrospectively detected by the Greyson scale.

MCQ (Memory Characteristics Questionnaire)one month after first interview

analyze of the phenomenological characteristics of real and imagined memories

Trial Locations

Locations (1)

University Hospital of Liège

🇧🇪

Liège, Belgium

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