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Incidence of Episodes of (Dis)Connected Consciousness Among Emergency Patients Admitted in the Resuscitation Room

Incidence of Episodes of (Dis)Connected Consciousness Among Emergency Patients Admitted in the Resuscitation Room

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06362525
Enrollment
100
Registered
2024-04-12
Start date
2023-10-09
Completion date
2027-09-30
Last updated
2024-04-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Consciousness, Loss of, Critical Illness, Emergencies, Near-Death Experience, Quality of Life

Keywords

Dream

Brief summary

This observational study aims to describe the incidence of episodes of disconnected consciousness (including near-death experience (NDE)) and episodes of connected consciousness in patients admitted to the resuscitation room, who survived a critical condition and who meet at least one of these criteria during their stay in the resuscitation room: (1) deep sedation, (2) intubation, (3) cardiopulmonary resuscitation, or (4) (non-drug-induced) Glasgow Coma Scale score = 3. We also investigate the potential (neuro)physiological markers and biomarkers. In order to help determine the potential risk factors of such episodes, cognitive factors such as dissociative propensity are also investigated. Unexpected visual and auditory stimuli will be displayed. In addition, we assess the evolution of memory, as well as short- and long-term consequences on quality of life, anxiety, and attitudes towards care. Memory of patients who did not meet the above-mentioned criteria are also investigated. A group of 15 healthy participants will be invited to test the stimuli display. Finally, (neuro)physiological parameters of a subsample of dying patients are also investigated.

Interventions

None listed

Sponsors

Centre Hospitalier Universitaire de Liege
CollaboratorOTHER
University of Liege
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* patients admitted in the resuscitation room of our university hospital * French speaking

Exclusion criteria

* Refusal * Chronic disorder of consciousness * Deafness * Blindness * Dementia * Hemineglect * Aphasia

Design outcomes

Primary

MeasureTime frameDescription
Detection of potential episodes of disconnected consciousnessupon awakening/discharge from the resuscitation room (max 21 days after the admission in the room)near-death experience (using the Near-Death Experience Content scale); dream
Detection of potential episodes of connected consciousnessupon awakening/discharge from the resuscitation room (max 21 days after the admission in the room)explicit recall of environmental/external stimuli upon awakening

Secondary

MeasureTime frameDescription
Risk factorsin the resusctiation room admission(neuro)physiological marker; biomarker; cognitive factor
Quality of life assessmentat 6-monthThe EuroQol five-dimension three-level questionnaire (EQ-5D-3L) comprises two sections. The first one is a five-question descriptive component which explores five dimensions (mobility, self-care, usual activities, pain/discomfort and anxiety/depression). Each question has three possible answers, rated from 1 to 3 (no problems, some problems and extreme problems). The second section is a visual analogue scale (EQ VAS; 0 worst imaginable health state to 100 best imaginable health state) about their current health state.
Memory content and evolution assessmentat 1-monthThe Memory Characteristics Questionnaire (MCQ). A total score can be derived summing all the 16 items (each on a 1-7 points Likert scale) and refers to as the amount of memory characteristics (i.e. higher total scores reflect greater amount of memory characteristics).
Detection of post-traumatic stress disorder (PTSD)at 6-monthThe Posttraumatic Stress Disorder Checklist 5 (PCL-5). Its total score can range from 0 to 80 (scores of ≥31 suggest a probable diagnosis of PTSD)

Countries

Belgium

Contacts

Primary ContactCharlotte Martial, PhD
cmartial@uliege.be+3243233612
Backup ContactPauline Fritz, Ms
pauline.fritz@uliege.be

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026