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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.

調査の概要

詳細な説明

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.

研究の種類

観察的

入学 (推定)

250

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究場所

    • Vilnius City
      • Vilnius、Vilnius City、リトアニア、LT-08660
        • National Cancer Center Affiliate of Vilnius University Hospital Santaros Klinikos
        • コンタクト:
        • 主任研究者:
          • Ernestas Sileika, MD

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

サンプリング方法

非確率サンプル

調査対象母集団

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.

説明

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

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 観測モデル:COHORT
  • 時間の展望:PROSPECTIVE

コホートと介入

グループ/コホート
介入・治療
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.

他の名前:
  • VOCALI

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Documentation Quality - AI-Generated Clinical Documentation Quality (PDQI-10)
時間枠: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
時間枠: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
時間枠: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)

二次結果の測定

結果測定
メジャーの説明
時間枠
Physician Subjective Workload (NASA-TLX)
時間枠: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)
時間枠: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
時間枠: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)
時間枠: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)

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

協力者

捜査官

  • 主任研究者:Ernestas Šileika、National Cancer Center Affiliate of Vilnius University Hospital Santaros Klinikos

出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年11月1日

一次修了 (推定)

2027年11月1日

研究の完了 (推定)

2027年12月31日

試験登録日

最初に提出

2026年9月23日

QC基準を満たした最初の提出物

2026年9月23日

最初の投稿 (実際)

2026年9月30日

学習記録の更新

投稿された最後の更新 (実際)

2026年9月30日

QC基準を満たした最後の更新が送信されました

2026年9月23日

最終確認日

2026年9月1日

詳しくは

本研究に関する用語

追加の関連 MeSH 用語

その他の研究ID番号

  • NVC-2026-001
  • 2026/5-1769-1212 (その他の識別子:Vilnius Regional Biomedical Research Ethics Committee)

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

IPD プランの説明

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.

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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