Awareness Detection and Communication in Disorders of Consciousness

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age10-80
SponsorUniversity of Ulster

About this trial

STUDY OVERVIEW Brain injury can result in a loss of consciousness or awareness, to varying degrees. Some injuries are mild and cause relatively minor changes in consciousness. However, in severe cases a person can be left in a state where they are "awake" but unaware, which is called unresponsive wakefulness syndrome (UWS, previously known as a vegetative state). Up to 43% of patients with a UWS diagnosis, regain some conscious awareness, and are then reclassified as minimally conscious after further assessment by clinical experts. Many of those in the minimally conscious state (MCS) and all with unresponsive wakefulness syndrome (UWS) are incapable of providing any, or consistent, overt motor responses and therefore, in some cases, existing measures of consciousness are not able to provide an accurate assessment. Furthermore, patients with locked-in syndrome (LIS), which is not a disorder of consciousness as patients are wholly aware, also, struggle to produce overt motor responses due to paralysis and anarthria, leading to long delays in accurate diagnoses using current measures to determine levels of consciousness and awareness. There is evidence that LIS patients, and a subset of patients with prolonged disorders of consciousness (DoC), can imagine movement (such as imagining lifting a heavy weight with their right arm) when given instructions presented either auditorily or visually - and the pattern of brain activity that they produce when imagining these movements, can be recorded using a method known as electroencephalography (or EEG). With these findings, the investigators have gathered evidence that EEG-based bedside detection of conscious awareness is possible using Brain- Computer Interface (BCI) technology - whereby a computer programme translates information from the users EEG-recorded patterns of activity, to computer commands that allow the user to interact via a user interface. The BCI system for the current study employs three possible imagined movement combinations for a two-class movement classification; left- vs right-arm, right-arm vs feet, and left-arm vs feet. Participants are trained, using real-time feedback on their performance, to use one of these combinations of imagined movement to respond to 'yes' or 'no' answer questions in the Q\&A sessions, by imagining one movement for 'yes' and the other for 'no'. A single combination of movements is chosen for each participant at the outset, and this participant-specific combination is used throughout their sessions. The study comprises three phases. The assessment Phase I (sessions 1-2) is to determine if the patient can imagine movements and produce detectable modulation in sensorimotor rhythms and thus is responding to instructions. Phase II (sessions 3-6) involves motor-imagery (MI) -BCI training with neurofeedback to facilitate learning of brain activity modulation; Phase III (sessions 7-10) assesses patients' MI-BCI response to closed questions, categorized to assess biographical, numerical, logical, and situational awareness. The present study augments the evidence of the efficacy for EEG-based BCI technology as an objective movement-independent diagnostic tool for the assessment of, and distinction between, PDoC and LIS patients.

Eligibility criteria

Qualifiers

Disorder of consciousness or low awareness state diagnosis ranging from unclear diagnosis in low awareness states, vegetative state and minimally conscious diagnosis. Those with locked in syndrome / completed locked in syndrome resulting from injury or disease e.g., motor neuron disease who do not have health problems that would preclude them from participating may be assessed but considered as a separate cohort to those with low awareness states.

acute, post-acute patients where appropriate

Disqualifiers

Participants with brain related diseases or illnesses (e.g., progressive neurological condition or uncontrolled epilepsy) or suffer from pain (these may adversely affect the brain data produced) and are deemed to be unsuitable for the trials by clinical teams.

Current consumption of medications that cause excessive fatigue or adversely affect cognitive functioning

Where English is not the individual's first language

Participant with excessive uncontrollable arm or head movement or teeth grinding as EEG signal quality will be degraded significantly.

Trial design

Treatments tested in this trial

  • Motor imagery based EEG-BCI

Treatment groups

30 Participants
are divided into 1 treatment group

Sponsors and collaborators

University of Ulster

Lead sponsor

National Rehabilitation Hospital, Dublin, Ireland (NRH)

Collaborator

Belfast Health and Social Care Trust

Collaborator

Western Health and Social Care Trust

Collaborator

Southern Health and Social Care Trust

Collaborator

Northern Health and Social Care Trust

Collaborator

Barnsley Hospital NHS Foundation Trust

Collaborator

NHS Lothian

Collaborator

Walton Centre NHS Foundation Trust

Collaborator

Hull University Teaching Hospitals NHS Trust

Collaborator

Imperial College Healthcare NHS Trust

Collaborator

Royal Hospital for Neuro-disability

Collaborator

South Warwickshire NHS Foundation Trust

Collaborator

Sheffield Teaching Hospitals NHS Foundation Trust

Collaborator

Oxford University Hospitals NHS Trust

Collaborator

Castel Froma Neuro Care

Collaborator

Inspire Neurocare

Collaborator

The Huntercombe Group

Collaborator

Active Care Group

Collaborator