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Study identifier: NCT07302906 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Ambient AI Scribe (Voa Health) in Outpatient Clinics: Draft Notes, Documentation Burden, and Well-Being

Condition: Burnout, Professionals · Medical Records Systems, Computerized · Physician-Patient Relations  ·  Sponsor: Pedro Angelo Basei de Paula

PhaseNA
Planned participants300
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this randomized clinical trial is to learn whether an "ambient AI scribe" (Voa Health) can reduce documentation burden and improve physician well-being and patient experience in outpatient clinics. The AI scribe listens to the audio of the consultation and produces a draft of the clinical note that the physician reviews and edits. In this study, consultations are randomized to 2 groups: usual documentation (without AI) or documentation assisted by the AI scribe. Adult patients seen in participating clinics, and their physicians, are invited to take part. For both groups, the consultation audio is recorded and, at the end of the visit, physicians and patients complete short questionnaires about well-being, workload, communication, empathy, and satisfaction. The questionnaires are based on internationally used scales (such as PFI, Mini-Z, NASA-TLX, CARE, PSQ-18, and CAT) but adapted to keep them brief and feasible in routine care. The main questions are whether the AI scribe lowers the time and effort needed to document the visit, improves physician professional fulfillment and reduces burnout, and whether it affects how patients perceive the communication, empathy, and overall quality of the consultation. No drugs or devices are being tested. The results are expected to guide hospitals on the safe and effective use of ambient AI scribes in real-world clinical practice.

This description comes directly from the study's public registry record.

Talk to the study team

Gustavo Lenci Marques, MD, PhD  ·  +5541991491428  ·  gustavolencimarques@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Complexo Hospital de Clínicas da UFPR (CHC-UFPR)Curitiba, Paraná, BrazilRecruiting

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Source record: clinicaltrials.gov/study/NCT07302906