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Eye-Tracking Interactive Agent in Non-verbal ICU Patients

Eye-Tracking Interactive Agent in Non-verbal ICU Patients: A Study Protocol of a Randomized Controlled Trial With an Embedded Qualitative Study

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07429695
Enrollment
54
Registered
2026-02-24
Start date
2026-04-01
Completion date
2027-12-31
Last updated
2026-02-24

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

Conditions

Eye Tracking, ICU, Communication Barriers, Non-Verbal Communication

Brief summary

The goal of this clinical trial is to determine whether an eye-tracking interactive agent can ameliorate communication impairments and reduce the incidence of complications among non-verbal patients in the intensive care unit (ICU). The main questions it aims to answer are: Does the eye tracking interactive agent alleviate communication impairments among non-verbal patients in the ICU? Does the eye tracking interactive agent improve communication efficiency among non-verbal patients in the ICU? Does the eye tracking interactive agent m reduce the incidence of negative emotions among non-verbal patients in the ICU? Does the eye tracking interactive agent shorten the ICU length of stay for non-verbal patients in the ICU? Does the eye tracking interactive agent reduce the dosage of analgesic and sedative medications for non-verbal patients in the ICU? Does the eye tracking interactive agent improve family satisfaction for non-verbal patients in the ICU? Does the eye tracking interactive agent alleviate nurses' communication burden among non-verbal patients in the ICU? Researchers will compare eye tracking interactive agent to conventional techniques to see if e eye tracking interactive agent works to alleviate communication impairments. Participants will: Use an eye tracking interactive agent for augmentative communication for 2 consecutive days Document each communication's details, ICU LOS, and analgesic-sedative dosages; assess communication difficulty severity, delirium, anxiety, family satisfaction and nurses' communication burden with validated scales.

Interventions

DEVICEeye-tracking interactive agent

The eye-tracking interactive agent consists of an eye-tracker, an iPad, and a floor-standing stand. Positioned at the patient's bedside, the system is activated upon the patient's eye opening, allowing the patient to vocalize via this eye-tracking interactive system.

Nurses communicate with patients through verbal inquiry, hand gestures, head nods or shakes, and simple paper-and-pencil tools; patients unable to write communicate solely via body language. Needs are guessed only when patients exhibit obvious discomfort.

Sponsors

Shanghai Zhongshan Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

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

Inclusion criteria

* Aged ≥ 18 years * Patients in the ICU who are unable to communicate through normal verbal means due to endotracheal intubation/tracheotomy, muscle or nerve injury, acute/chronic spinal cord injury, etc. * Richmond Agitation-Sedation Scale (RASS) score of -1 to 1 * Primary caregivers are adults * Able to read Chinese characters and follow simple commands * Willing to participate in this study.

Exclusion criteria

* Diseases associated with cognitive impairment, such as pulmonary encephalopathy, hepatic encephalopathy, diabetic hyperosmolar coma, and coma of unknown cause * A history of mental disorders, dementia or pre-dementia, or intellectual disability * Conditions precluding cooperation with eye-tracking interaction, such as blindness or inability to elevate the eyelids.

Design outcomes

Primary

MeasureTime frameDescription
Communication difficultyup to 2days after enrollmentThe degree of communication difficulty in non-verbal ICU patients will be assessed using the Ease of Communication Scale. This tool was revised by Menzel et al. in 1998 and has previously been used to assess communication difficulties among non-verbal patients in the ICU. The scale comprises 6 items, with response options ranging from 0 (no difficulty at all) to 4 (extreme difficulty). The total score ranges from 0 to 24, with higher scores indicating greater communication difficulties.

Secondary

MeasureTime frameDescription
Communication efficiencyup to 2 days after enrollmentthe number of successful communications within 24 hours
Anxietyat 4:00 PM dailyAnxiety level will be measured using the Faces Anxiety Scale. This is a single-item scale with five response options, ranging from neutral expression (1 point) to extreme anxiety (5 points).
Delirium-free daysthrough discharge from the ICU,an average of 1 weekDelirium-free days refer to the total number of complete calendar days without delirium during the ICU stay.
Physiological outcomes (heart rate)up to 2 days after enrollmentThe patient's heart rate will be recorded at the start of each communication, and the variability of heart rate during communication will be calculated.
Physiological outcomes (blood pressure)up to 2 days after enrollmentThe patient's blood pressure will be recorded at the start of each communication, and the variability of blood pressure during communication will be calculated.
Length of ICU staythrough discharge from the ICU,an average of 1 weekThe total length of the patient's ICU stay will be recorded.
Dosage of analgesic and sedative medicationsup to 2 days after enrollmentThe daily dosage of analgesic and sedative medications administered to the patient will be recorded.
Satisfaction of primary caregiversthrough discharge from the ICU,an average of 1 weekFamily satisfaction will be assessed using the Family Satisfaction in the ICU-24 (FS-ICU-24) scale. This scale consists of 24 items and has been well validated for measuring satisfaction among family members of patients admitted to the ICU. The scale comprises two domains: satisfaction with care and satisfaction with decision-making. Each item is scored on a continuous scale ranging from 0 to 100. The domain score is calculated as the sum of all valid item scores within that domain divided by the number of valid items in the respective domain. The total FS-ICU-24 score is computed as the sum of the two domain mean scores divided by 2, with higher scores representing a higher level of satisfaction.
Communication burden of medical staffsthrough study completion,an average of 1 yearThe communication burden of ICU nurses was assessed using the NASA Task Load Index (NASA-TLX). This scale has been widely used to evaluate the subjective workload of healthcare providers and covers six domains: mental demand, physical demand, temporal demand, performance level, effort, and frustration. Each of the six domains is scored on a continuous scale ranging from 0 to 100, where a score of 0 indicates the lowest level of the domain and a score of 100 indicates the highest level.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 25, 2026