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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.

Studieoversikt

Status

Har ikke rekruttert ennå

Detaljert beskrivelse

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.

Studietype

Observasjonsmessig

Registrering (Antatt)

250

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studiesteder

    • Vilnius City
      • Vilnius, Vilnius City, Litauen, LT-08660
        • National Cancer Center Affiliate of Vilnius University Hospital Santaros Klinikos
        • Ta kontakt med:
        • Hovedetterforsker:
          • Ernestas Sileika, MD

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Prøvetakingsmetode

Ikke-sannsynlighetsprøve

Studiepopulasjon

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.

Beskrivelse

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

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Observasjonsmodeller: COHORT
  • Tidsperspektiver: PROSPECTIVE

Kohorter og intervensjoner

Gruppe / Kohort
Intervensjon / Behandling
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.

Andre navn:
  • VOCALI

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Documentation Quality - AI-Generated Clinical Documentation Quality (PDQI-10)
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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)

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Physician Subjective Workload (NASA-TLX)
Tidsramme: 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)
Tidsramme: 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
Tidsramme: 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)
Tidsramme: 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)

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Samarbeidspartnere

Etterforskere

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

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

1. november 2026

Primær fullføring (Antatt)

1. november 2027

Studiet fullført (Antatt)

31. desember 2027

Datoer for studieregistrering

Først innsendt

23. september 2026

Først innsendt som oppfylte QC-kriteriene

23. september 2026

Først lagt ut (Faktiske)

30. september 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

30. september 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

23. september 2026

Sist bekreftet

1. september 2026

Mer informasjon

Begreper knyttet til denne studien

Ytterligere relevante MeSH-vilkår

Andre studie-ID-numre

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

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

IPD-planbeskrivelse

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.

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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