REVEIL: Feasibility Study of Virtual Reality to Promote the Awakening of Patients in a State of Minimal Consciousness

Sponsor
University Hospital, Angers (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT04978857
Collaborator
(none)
8
1
1
43
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Study Details

Study Description

Brief Summary

Advances in neurosurgery and neuroresuscitation have improved patients' prognosis. However, 2% of serious head injuries progress to a vegetative state, this condition persisting at 1 year for 1% of these patients.

The minimum state of consciousness is to be distinguished from coma and vegetative state, it is a condition marked by a severe alteration of consciousness in which there are minimal and fluctuating, but obvious, signs of environmental consciousness. There is a minimum degree of response to some stimulations, response generally fluctuating over time. In practice, these patients are unable to consistently follow simple instructions, but they often have a preserved visual pursuit (proper rotation of the head when someone enters the room, prolonged eye follow-up, etc.). Patients with minimal awareness have been shown to perceive emotions and pain. These patients may exhibit behavioural and emotional changes (smiling, crying motivated), induced by verbal stimulations (familiar voice). But these events remain fluctuating during the day or according to the days and interlocutors.

For the moment, the most commonly accepted strategy since the 1990s remains sensory stimulation (SS), while knowing that this term includes extremely varied stimulations (sensory, olfactory, auditory, fixation on a mirror, etc.) without the practice of this technique being well defined and systematized.

It has been shown that a regular family visit program with auditory, emotional and tactile stimuli improves the state of consciousness of these patients. Physicians also know that this SS must be personalized and adapted to the patient's tolerance and premorbid preferences.

SS programmes are poorly standardized. Programmes generally consist of a simple, moderate to high intensity, non-standardized stimulation, presented repetitively and frequently. Indeed, it has been shown that stimulation must begin early, be frequent, and continue until reactions appear.

In this project, investigator want to use the new technologies now commonly used such as photos, videos or sounds taken by smartphone's relatives of the brain patient-injured in order to make a personalized 3D film using film editing software and a predefined film frame, by integrating autobiographical elements and emotional, multisensory (binaural sound, vibration) integrating, if possible, a certain interactivity (haptic feedback, triggering of videos by the patient's eyes).

The objective is to develop an innovative multi-sensory stimulation technique through a personalised enriched environment to induce, facilitate and accelerate the return to consciousness of patients in altered state of consciousness during their initial management.

Condition or Disease Intervention/Treatment Phase
  • Other: autobiographic movie
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
8 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Feasibility Study of Virtual Reality to Promote the Awakening of Patients in a State of Minimal Consciousness
Anticipated Study Start Date :
Sep 1, 2021
Anticipated Primary Completion Date :
Oct 1, 2024
Anticipated Study Completion Date :
Apr 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Virtual reality headset

Other: autobiographic movie
viewing an autobiographic film through a virtual reality headset

Outcome Measures

Primary Outcome Measures

  1. percentage of patients without any adverse event or sign of bad tolerance [1 month]

    to assess the feasibility of multisensory virtual reality stimulation proposed in this study in patients with minimal post-traumatic consciousness

Secondary Outcome Measures

  1. Time required for film design [2 weeks]

    to assess the feasibility of making a personalized film

  2. type and quantity of autobiographical material to be obtained from the patient's relatives [2 weeks]

    to assess the feasibility of making a personalized film

  3. Patient clinical responses (blood pressure, body motion, eye-tracking) [1 month]

    To assess signs of patient's interaction with the virtual reality headset during the pre-inclusion phase and during the test phase, and the evolution over time of these signs during the test phase

  4. Wessex Head Injury Matrix (WHIM) [6 month]

    To assess the evolution of the patient's clinical status Scale from 0 which means vegetative state to 62 which means pauci-relational state

  5. Coma Recovery Scale - Revised (CRS-R) [6 month]

    To assess the evolution of the patient's clinical status

  6. functional MRI [1 month]

    To assess and compare the different brain networks identified during the fMRI performed one week after the initial fMRI test phase performed the week preceding the test phase.

  7. patient's relative satisfaction scale [1 month]

    To assess patient's family's feelings and experiences with this intervention (interviews etc). Scale from 1 (minimum) to 7 (maximum); 1 means not satisfied at all and 7 means very satisfied

  8. healthcare team satisfaction scale [1 month]

    To assess healthcare team feelings and experiences with this intervention (adherence to this rehabilitation technique etc) Scale from 1 (minimum) to 7 (maximum); 1 means not satisfied at all and 7 means very satisfied

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patient diagnosed with minimal consciousness

  • Patient affiliated or beneficiary of a social security scheme

  • Signature of consent by a relative of the patient

  • Tolerance of the multisensory stimulation material during the pre-inclusion phase

Exclusion Criteria:
  • Minor

  • Pregnant woman

  • Patient with contraindication to study procedures (Contraindication to wearing a virtual reality headset (unbalanced epilepsy, craniofacial trauma, major visual disturbances; contraindication to the fMRI)

  • Person deprived of liberty by judicial or administrative decision

  • Person receiving psychiatric care under duress

Contacts and Locations

Locations

Site City State Country Postal Code
1 CHU Angers Angers France

Sponsors and Collaborators

  • University Hospital, Angers

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital, Angers
ClinicalTrials.gov Identifier:
NCT04978857
Other Study ID Numbers:
  • 49RC20_0238
First Posted:
Jul 27, 2021
Last Update Posted:
Aug 4, 2021
Last Verified:
Mar 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 4, 2021