Eye Movements to Predict Post-Operative Delirium (EYE-POD)
Predicting Post-operative Delirium Using Eye Movements: a Pilot Study
연구 개요
상태
상태
정황
정황
상세 설명
This prospective trial evaluates the integration of automated eye movement assessments as a novel, noninvasive risk biomarker for postoperative delirium (POD) in older adults. Upon enrollment, trained clinical staff will collect baseline demographic data and clinical characteristics. Chronic medical burden will be quantified using the Charlson Comorbidity Index (CCI). To establish baseline cognitive function and control for preexisting cognitive impairment, all participants will undergo the Montreal Cognitive Assessment (MoCA).
Technical Protocol for Eye Movement Recording
Preoperatively, participants will complete an automated eye movement tracking protocol consisting of two distinct paradigms:
Prosaccadic Task: Utilized to measure specific ocular motor parameters, including saccadic latency, velocity, and accuracy.
Free Visual Exploration Task: Utilized to capture free-gaze metrics and spatial distribution patterns.
All eye-tracking data will be recorded using automated software to ensure objectivity and reproducibility.
Postoperative Monitoring Following the surgical procedure, patients will be systematically monitored for the development of POD. The Confusion Assessment Method (CAM) will be administered by trained examiners twice daily (morning and evening) for the first three postoperative days (72 hours) to detect and document the incidence and severity of delirium.
Statistical and Predictive Objectives
The collected data will be analyzed to fulfill three primary scientific objectives:
- Parameter Association: To identify which specific preoperative eye-tracking metrics (latency, velocity, accuracy, or free-gaze variables) demonstrate a statistically significant association with the incidence of POD.
- Diagnostic Performance: To calculate the sensitivity and specificity of these distinct preoperative eye movement parameters for predicting POD development.
- Incremental Predictive Value: To evaluate whether adding preoperative eye-tracking measurements to a standard clinical prediction model (comprising age, sex, CCI, and MoCA scores) significantly improves the model's overall predictive performance and risk stratification capabilities.
연구 유형
연구 유형
등록 (추정된)
등록
연락처 및 위치
연구 장소
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Santiago Metropolitan
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Santiago, Santiago Metropolitan, 칠레, 8320000
- Hospital Clínico de la Universidad de Chile
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참여기준
자격 기준
자격 기준
공부할 수 있는 나이
- 고령자
건강한 자원 봉사자를 받아들입니다
샘플링 방법
연구 인구
설명
Inclusion Criteria:
- Patients aged 70 years or older.
- Scheduled for moderate- to high-risk elective surgery, defined as a procedure requiring a postoperative hospital stay of at least 3 days.
- Able to provide signed, written informed consent.
Exclusion Criteria:
- Presence of delirium at baseline admission, evaluated via the Confusion Assessment Method (CAM).
- Use of neuroleptic/antipsychotic medications within the past 6 months.
- Prior history of dementia (including Alzheimer's disease, vascular dementia, or mild cognitive impairment).
- History of encephalopathy.
- Psychiatric disorders presenting with psychosis.
- Brain injury with neurological sequelae (e.g., prior stroke, traumatic brain injury).
- Visual acuity is insufficient to complete the automated eye-tracking tasks.
- Illiteracy.
- Non-Spanish speakers.
- Concurrent participation in any other clinical trial.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
그룹/코호트 수
코호트 및 개입
그룹/코호트그룹/코호트 |
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No Intervention: Control (Usual care) + Eye movement recording
This is a prospective, observational cohort study designed to evaluate the prognostic accuracy of a preoperative eye-tracking biomarker protocol for predicting postoperative delirium (POD). All eligible participants are recruited from a cohort of patients already scheduled for moderate- to high-risk elective surgery at the University of Chile Clinical Hospital. The study procedures (baseline clinical data collection, Charlson Comorbidity Index, MoCA, and automated eye-tracking tasks) are strictly observational and diagnostic. The eye-tracking results are recorded for research purposes only and do not alter standard perioperative care, surgical management, or anesthetic techniques. Patients are subsequently followed into the postoperative period to monitor the incidence of POD via twice-daily Confusion Assessment Method (CAM) evaluations during the first three postoperative days. |
연구는 무엇을 측정합니까?
주요 결과 측정
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
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Incidence of postoperative delirium (POD).
기간: From the day of surgery up to postoperative day 3, patients were assessed twice daily.
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The presence or absence of postoperative delirium will be assessed using the Confusion Assessment Method (CAM).
Patients will be classified as "POD" or "No POD" based on the CAM diagnostic algorithm.
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From the day of surgery up to postoperative day 3, patients were assessed twice daily.
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2차 결과 측정
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Preoperative Baseline Cognitive Status
기간: At preoperative baseline (day of surgery or day before).
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Total score on the Montreal Cognitive Assessment (MoCA) to determine baseline global cognitive function.
The score ranges from 0 to 30, with lower scores indicating greater cognitive impairment.
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At preoperative baseline (day of surgery or day before).
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Preoperative Comorbidity Burden
기간: At preoperative baseline (day of surgery or day before)
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Score on the Charlson Comorbidity Index (CCI) to quantify the participant's baseline medical comorbidity burden and pre-existing health conditions.
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At preoperative baseline (day of surgery or day before)
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Preoperative Saccadic Latency
기간: At preoperative baseline (day of surgery or day before)
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The time taken from the appearance of a visual target to the initiation of the participant's saccadic eye movement during the prosaccadic task (milliseconds).
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At preoperative baseline (day of surgery or day before)
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Preoperative Saccadic Velocity
기간: At preoperative baseline (day of surgery or day before).
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The peak speed of the participant's eye movement when moving towards the visual target during the prosaccadic task (degrees per second).
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At preoperative baseline (day of surgery or day before).
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Preoperative Free Viewing Number of Fixations
기간: At preoperative baseline (day of surgery or day before).
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The absolute count of discrete gaze fixations made by the participant during the free visual exploration task (number of fixations)
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At preoperative baseline (day of surgery or day before).
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Preoperative Free Viewing Saccade Length
기간: At preoperative baseline (day of surgery or day before).
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The average spatial distance between fixations in the participant's eye movements during the free visual exploration task (degrees of visual angle).
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At preoperative baseline (day of surgery or day before).
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Hospital Length of Stay
기간: Up to 30 days post-surgery.
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Total hospital stay from the day of surgery until official hospital discharge.
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Up to 30 days post-surgery.
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All-Cause Mortality
기간: At 30 days post-surgery.
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Total number of participant deaths from any cause, verified via hospital electronic medical records or direct follow-up contact.
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At 30 days post-surgery.
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공동 작업자 및 조사자
수사관
수사관
- 수석 연구원: Ivan Plaza-Rosales, PhD, University of Chile
간행물 및 유용한 링크
일반 간행물
- Al-Hindawi A, Vizcaychipi M, Demiris Y. A Dual-Camera Eye-Tracking Platform for Rapid Real-Time Diagnosis of Acute Delirium: A Pilot Study. IEEE J Transl Eng Health Med. 2024 May 7;12:488-498. doi: 10.1109/JTEHM.2024.3397737. eCollection 2024.
- van der Kooi AW, Rots ML, Huiskamp G, Klijn FA, Koek HL, Kluin J, Leijten FS, Slooter AJ. Delirium detection based on monitoring of blinks and eye movements. Am J Geriatr Psychiatry. 2014 Dec;22(12):1575-82. doi: 10.1016/j.jagp.2014.01.001. Epub 2014 Jan 4.
- Chapin BA, Kimmett F, Garvan C, Tighe P, Dekosky S, Williamson JB, Price CC. Preoperative Visual Attention Performance Predicts Postoperative Delirium. Alzheimers Dement. 2025 Jan 3;20(Suppl 3):e091620. doi: 10.1002/alz.091620. PMCID: PMC11710506.
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
연구 시작
기본 완료 (추정된)
기본 완료
연구 완료 (추정된)
연구 완료
연구 등록 날짜
최초 제출
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QC 기준을 충족하는 최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
처음 게시됨
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
마지막 업데이트 게시됨
QC 기준을 충족하는 마지막 업데이트 제출
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추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
기타 연구 ID 번호
- 159526
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
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