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Ambient AI Documentation in Oncology Consultations (NVC-AI-DOC)

Feasibility Study of Ambient Artificial Intelligence Documentation Systems for Oncology Consultations at the National Cancer Center

This study tests whether an artificial intelligence (AI) system can help doctors write medical notes during cancer consultations.

After a cancer patient is seen by a multidisciplinary team (a group of specialists who decide on the best treatment), they have a consultation with their oncologist to discuss the treatment plan. During this consultation, doctors must write detailed medical notes, which takes significant time and effort.

In this study, an ambient AI system called VOCALI is used during oncology consultations at the National Cancer Center in Vilnius, Lithuania. Before the consultation begins, the doctor loads relevant pseudonymized clinical data from the electronic health record (such as diagnosis and treatment plan) into the system. During the consultation, VOCALI records the conversation (with the patient's consent) and combines it with the loaded clinical data to automatically generate a draft medical note in Lithuanian. Patients may ask the doctor to stop the recording at any time. The doctor then reviews the draft, makes any necessary corrections, and approves the final document. The AI does not make any medical decisions - the doctor is always responsible for the final note.

What the study measures:

The study has three main goals:

  • To assess the quality of the AI-generated notes, rated by two independent reviewers using the PDQI-10, a standardized documentation quality instrument translated into Lithuanian using forward-backward translation
  • To measure the time doctors spend reviewing and approving the AI-generated draft
  • To monitor safety - whether any AI errors could affect patient care

The study also collects information on doctor workload, ease of use of the system, and patient satisfaction with the consultation.

Who can participate:

Adult patients (age 18 or older) attending a primary oncology consultation at the National Cancer Center in Vilnius, Lithuania, after a multidisciplinary team decision, who speak Lithuanian and provide written consent.

Study details:

250 patients will be enrolled over 12 months. Each participant attends one consultation and completes a short satisfaction questionnaire (about 5 minutes). No additional visits are required. There is no comparator group - all participants receive the AI-assisted documentation.

This is the first study to evaluate ambient AI documentation in the Lithuanian language and in the Lithuanian oncology setting.

연구 개요

상세 설명

BACKGROUND Electronic health record (EHR) documentation imposes a substantial administrative burden on physicians and is a major contributor to professional burnout. Studies consistently show that clinicians spend up to half their working time on computer-based documentation, leaving less than 30% of the working day for direct patient contact. Ambient AI documentation systems have shown reductions in documentation time and cognitive load across multiple health systems in the United States and Europe, with AI-generated note quality approximating that of physician-authored notes as measured by a modified Physician Documentation Quality Instrument (PDQI-9). No studies have evaluated ambient AI documentation in the Lithuanian language or in the Lithuanian oncology setting.

STUDY DESIGN Prospective, single-group, single-center feasibility study conducted at the National Cancer Center (NVC), Vilnius, Lithuania. No randomization or control arm.

AI DOCUMENTATION SYSTEM The VOCALI ambient AI system is activated at the start of each eligible consultation. Before the consultation, the physician loads pseudonymized clinical data from the EHR (diagnosis, MDT decision, treatment plan) into the system. The system audio-records the consultation in real time, integrates the preloaded clinical data, and generates a structured draft of the E025 outpatient clinical note in Lithuanian. The physician reviews, edits if necessary, and approves the final document in the EHR. The system does not make autonomous clinical decisions.

PROCEDURES

  • Informed consent obtained before consultation, including consent to audio recording.
  • PSQ-18 patient satisfaction questionnaire completed by participants on the same day post-consultation (~5 min).
  • PDQI-10 documentation quality instrument rated by two independent raters per AI-generated note.
  • NASA-TLX physician workload questionnaire administered at baseline (T0), 1 month (T1), and end of enrollment (T2).
  • SUS system usability scale completed by physicians at T2.
  • Documentation time and draft editing extent (% characters changed) logged automatically by the system.
  • Safety incidents reported by physicians within 3 working days; monthly safety review meeting held; immediate notification of the NVC Deputy Director for Medicine and the ethics committee required for level-5 (critical) incidents.

SAMPLE SIZE 250 participants will be enrolled over a 12-month period. As a feasibility study, sample size was determined by practical feasibility and literature precedent rather than formal power calculation. With n = 250, proportions can be estimated with a 95% CI of approximately ±3-4%; if no critical incident is observed, the upper 95% confidence limit is 1.2% (rule of three). Approximately 20% data loss is anticipated.

STATISTICAL ANALYSIS R ≥4.0 or SAS ≥9.4. Descriptive statistics for all outcomes. PDQI-10 mean score with 95% CI and domain-level analysis; documentation time as mean with 95% CI and median with IQR; SUS mean with 95% CI; PSQ-18 subscale means. Inter-rater reliability assessed by rWG coefficient (target ≥0.7). Critical incident rate reported with 95% CI using the Clopper-Pearson method. NASA-TLX change (T2-T0) analyzed by paired t-test or Wilcoxon signed-rank test depending on distribution. All inferential tests are descriptive in intent; results interpreted via confidence intervals.

DATA PROTECTION All participant data are pseudonymized immediately upon enrollment. Audio recordings and transcripts are stored in the VOCALI provider's secure infrastructure under a data processing agreement per GDPR Article 28; the provider has no access to identifiable participant data. Data retained for 5 years after study completion.

연구 유형

관찰

등록 (추정된)

250

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 장소

    • Vilnius City
      • Vilnius, Vilnius City, 리투아니아, LT-08660
        • National Cancer Center Affiliate of Vilnius University Hospital Santaros Klinikos
        • 연락하다:
        • 수석 연구원:
          • Ernestas Sileika, MD

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 이상 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

샘플링 방법

비확률 샘플

연구 인구

Adult oncology patients attending a primary oncologist consultation at the National Cancer Center (Vilnius, Lithuania) following a multidisciplinary team (MDT) decision, with diagnosis and treatment plan established.

설명

Inclusion Criteria:

  • Age 18 years or older at the time of signing the informed consent form
  • Primary oncologist consultation at the National Cancer Center following a multidisciplinary team (MDT) decision, with diagnosis and treatment plan established at the MDT meeting
  • MDT protocol available in the electronic health record (EHR)
  • Signed informed consent form, including consent to audio recording of the consultation

Exclusion Criteria:

  • Absence of MDT protocol in the EHR
  • Diagnosis or treatment plan not yet established
  • MDT recommended additional diagnostic workup (treatment plan not yet defined)
  • Palliative care consultation (not active oncological treatment planning)
  • Non-Lithuanian speaking patients
  • Cognitive impairment affecting ability to understand study information
  • Hearing impairment affecting participation in verbal consultation

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 관찰 모델: COHORT
  • 시간 관점: PROSPECTIVE

코호트 및 개입

그룹/코호트
개입 / 치료
Oncology patients undergoing AI-assisted consultation

Adult oncology patients attending a primary oncologist consultation at the National Cancer Center following a multidisciplinary team (MDT) decision, during which the VOCALI ambient AI documentation system is used to generate a draft clinical note (E025 form).

An ambient artificial intelligence documentation system that records the consultation audio, integrates relevant pseudonymized clinical data from the electronic health record (EHR), generates a speech transcript, and produces a draft clinical note (E025 form) for physician review and approval. The system does not make autonomous clinical decisions. The physician reviews, edits if necessary, and approves all AI-generated content before it is saved to the EHR.

다른 이름들:
  • VOCALI

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Documentation Quality - AI-Generated Clinical Documentation Quality (PDQI-10)
기간: Per consultation, throughout the enrollment period (up to 12 months)

Mean score assessed by two independent raters using the Physician Documentation Quality Instrument (PDQI-10), covering 10 domains (accuracy, completeness, usefulness, organization, clarity, conciseness, synthesis, consistency, data accuracy, and bias) on a 1-5 Likert scale.

Per consultation, throughout the enrollment period (up to 12 months)
Documentation Efficiency - Documentation Completion Time
기간: Per consultation, throughout the enrollment period (up to 12 months)

Time (in minutes) from opening the AI-generated draft to final approval in the electronic health record (EHR), automatically recorded by the system.

Per consultation, throughout the enrollment period (up to 12 months)
Safety - AI System Incident Rate
기간: Per consultation, throughout the enrollment period (up to 12 months)

Frequency of AI documentation incidents classified by a 5-level severity scale (1 = insignificant, 2 = minor, 3 = moderate, 4 = major, 5 = critical). Incidents reported by physicians within 3 working days. Critical incident (level 5) rate reported with 95% confidence interval using the Clopper-Pearson method.

Per consultation, throughout the enrollment period (up to 12 months)

2차 결과 측정

결과 측정
측정값 설명
기간
Physician Subjective Workload (NASA-TLX)
기간: Baseline (T0), 1 month (T1), and end of enrollment period (T2, up to 12 months)

Physician-reported workload assessed using the NASA Task Load Index (NASA-TLX), covering 6 dimensions (mental demand, physical demand, temporal demand, performance, effort, frustration). Change from baseline (T0) to end of enrollment (T2) analyzed by paired t-test or Wilcoxon signed-rank test.

Baseline (T0), 1 month (T1), and end of enrollment period (T2, up to 12 months)
System Usability (SUS)
기간: End of enrollment period (T2, up to 12 months)

Physician-rated system usability assessed using the System Usability Scale (SUS), a 10-item questionnaire scored 0-100.

End of enrollment period (T2, up to 12 months)
AI Draft Editing Extent
기간: Per consultation, throughout the enrollment period (up to 12 months)

Proportion of characters modified between the AI-generated draft and the final approved document, expressed as percentage. Automatically calculated per consultation.

Per consultation, throughout the enrollment period (up to 12 months)
Patient Satisfaction with Consultation (PSQ-18)
기간: After each consultation, throughout the enrollment period (up to 12 months)

Patient-reported satisfaction assessed using the Patient Satisfaction Questionnaire (PSQ-18), an 18-item instrument. Results reported as subscale means.

After each consultation, throughout the enrollment period (up to 12 months)

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

협력자

수사관

  • 수석 연구원: Ernestas Šileika, National Cancer Center Affiliate of Vilnius University Hospital Santaros Klinikos

간행물 및 유용한 링크

연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 11월 1일

기본 완료 (추정된)

2027년 11월 1일

연구 완료 (추정된)

2027년 12월 31일

연구 등록 날짜

최초 제출

2026년 9월 23일

QC 기준을 충족하는 최초 제출

2026년 9월 23일

처음 게시됨 (실제)

2026년 9월 30일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 9월 30일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 9월 23일

마지막으로 확인됨

2026년 9월 1일

추가 정보

이 연구와 관련된 용어

추가 관련 MeSH 약관

기타 연구 ID 번호

  • NVC-2026-001
  • 2026/5-1769-1212 (기타 식별자: Vilnius Regional Biomedical Research Ethics Committee)

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

아니요

IPD 계획 설명

Individual participant data will not be shared. The ethics-approved protocol and the informed consent do not provide for transfer of individual data to third parties, in accordance with the EU General Data Protection Regulation (GDPR) 2016/679 and Lithuanian data protection legislation. The data include consultation audio recordings and clinical documentation. Only aggregated results will be published in scientific journals and presented at conferences.

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

구독하다