Unresponsive Wakefulness Syndrome

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Review clinical trials related to Unresponsive Wakefulness Syndrome. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

fNIRS for Disorders of Consciousness

The goal of this observational study is to learn whether functional near-infrared spectroscopy (fNIRS) can measure brain activity in healthy adults and in people with disorders of consciousness (DoC) in the neuro-intensive care unit (Neuro-ICU). DoC include conditions such as coma and minimally conscious state that occur after severe brain injury. These conditions make it difficult to assess a person's level of awareness because many clinical tests rely on observable behaviors such as speaking or moving, which are commonly impaired after brain injury. The main questions the study aims to answer are: * Can fNIRS detect changes in brain activity in healthy adults when they receive sensory stimulation or perform mental tasks? * Can the same fNIRS protocol be used in patients with disorders of consciousness in the Neuro-ICU to measure brain responses and determine whether the method is feasible in this clinical setting? The investigators will first study healthy adult volunteers to establish baseline brain responses and determine which tasks produce the most reliable signals. The protocol will then be applied to patients with disorders of consciousness admitted to the Neuro-ICU. Participants will take part in a single research session lasting about 30 to 45 minutes while wearing the lightweight fNIRS headband that measures brain oxygen levels using near-infrared light. During the session, participants will: * Wear a non-invasive fNIRS headband placed on the forehead * Receive gentle sensory stimulation (for example, compression devices on the legs or hands) * Listen to sounds or spoken sentences * Perform guided mental tasks such as imagining walking through their home or imagining moving a limb The study does not test a treatment and will not change medical care. The goal is to determine whether fNIRS can safely and reliably measure brain activity at the bedside and provide preliminary information that may help guide future research on improving the assessment of consciousness after brain injury.

Participants needed: 55
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University of California, Los AngelesUpdated: Jun 8, 2026Locations: 1
Eligibility criteria

Age 18 years or older [+9]

Known baseline hearing impairment without available hearing aids [+7]

Status: Recruiting

Assessment of Consciousness With CRS-R and SECONDs

Accurately determining the level of consciousness in patients with severe brain injury is essential for treatment planning, prognosis, and ethical decision-making. Clinically, levels of consciousness are differentiated into coma, Unresponsive Wakefulness Syndrome (UWS), and Minimally Conscious State (MCS) based on behavioral signs. Although behavioral assessment is considered the clinical gold standard, it is prone to misclassification. Research has shown that a substantial proportion of patients initially diagnosed with UWS may actually show signs of minimal consciousness, which is associated with better cognitive abilities and a more favorable prognosis. The Coma Recovery Scale-Revised (CRS-R) is internationally recommended for diagnosing disorders of consciousness, but it is time-consuming and not free from diagnostic error. Repeated assessments can significantly improve diagnostic accuracy. To enhance feasibility in routine clinical practice, a shorter and more time-efficient assessment tool, the Simplified Evaluation of CONsciousness Disorders (SECONDs), was developed. This scale focuses on the behavioral signs most strongly associated with MCS and uses optimized testing procedures while maintaining high diagnostic accuracy. The aim of this study is to further evaluate diagnostic approaches for assessing consciousness in patients with severe brain injury and to improve the reliability and clinical applicability of these assessments.

Participants needed: 110
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: BDH-Klinik Hessisch OldendorfUpdated: Mar 11, 2026Locations: 1
Eligibility criteria

Admission to an intensive care unit (ICU) or intermediate/high-dependency care u... [+3]

History of prior brain injury [+5]

Status: Not yet recruiting

Auditory Processing in DOC Patients

This prospective observational study investigates whether electroencephalography (EEG) can improve the differentiation between unresponsive wakefulness syndrome (UWS) and minimally conscious state (MCS) in patients with severe acquired brain injury. The study further examines the association between EEG markers of auditory processing and long-term functional outcome at 12 months.

Participants needed: 42
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: BDH-Klinik Hessisch OldendorfUpdated: Mar 6, 2026Locations: 1
Eligibility criteria

Presence of a disorder of consciousness (Unresponsive Wakefulness Syndrome [UWS]... [+3]

Ongoing sedation at the time of EEG assessment [+7]

Status: Recruiting

Transcranial Temporal Interference Stimulation In Severely Brain Injured Patients With Disorders of Consciousness

The purpose of this academic lead study is to explore the effect of noninvasive neuromodulation of the CM-pf via tTIS for patients with disorders of consciousness.

Participants needed: 10
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Xijing HospitalUpdated: Apr 9, 2025Locations: 2
Eligibility criteria

traumatic and nontraumatic etiology of VS/UWS or MCS according to published diag...

patients in coma, with less than 1 week after acute brain insult, with fluctuati...