Can an AI listener write therapy notes without breaking the Doctor-Patient bond?
NCT ID NCT07777224
First seen Aug 20, 2026 · Last updated Aug 21, 2026 · Updated 1 time
Summary
This trial tests whether an AI tool that listens to psychiatric consultations and drafts clinical notes can reduce the time clinicians spend on paperwork. It includes mental health providers and their adult patients at a Swiss psychiatric clinic. Researchers will compare clinicians using the AI to those writing notes as usual, measuring documentation time, note quality, and the patient-rated therapeutic relationship. The goal is to see if the AI can ease administrative burden without harming the quality of care or the connection between clinician and patient.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- An artificial intelligence ambient scribe that listens to consultations and drafts clinical notes
- What this could lead to
- If effective, this AI tool could reduce clinician burnout and free up time for patient care, while maintaining the quality of medical records and the therapeutic relationship.
- What could go wrong
- The trial is small and early, and the AI may not produce notes as good as those written by clinicians, or patients might feel the tool affects their connection with their provider.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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47 people
The number who actually took part.
- Started
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Jul 2026
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
The observed study population comprises mental health care providers (physicians, psychologists/psychotherapists, nurses, and social workers) employed at Psychiatrie St. Gallen. Provider Inclusion Criteria: * Readiness to use an artificial intelligence ambient scribe during patient consultations (intervention group) * Regular clinical consultations with adult psychiatric patients Two outcome-specific criteria apply: contribution to the report quality outcomes requires that the provider regularly conducts new-patient intakes and writes initial psychiatric assessment reports; contribution to the patient-reported outcomes requires working in the outpatient setting. Providers who cannot or no longer wish to contribute to any actively collected outcome may, with their consent, remain enrolled for passive documentation-time measurement only; for analysis, such providers stay in the group which was fixed at enrollment.. Provider Exclusion Criteria: * notice of termination of the employment contract given during the data collection period * Working in the dementia inpatient clinic Patients are not the observed population, but anonymous ratings of their subjective consultation experience are collected from them, and written consent for the review of initial assessment reports is obtained. Patient Inclusion Criteria: \- All adult patients visiting the outpatient clinic during the data collection periods for a consultation with a participating provider Patient Exclusion Criteria: * Insufficient German proficiency (below level B2) * Cognitive impairment precluding informed participation * Acute psychosis, acute suicidality, mania, or intoxication * Severe emotional distress
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Psychiatrie St. Gallen
Heerbrugg, Canton of St. Gallen, 9435, Switzerland
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Psychiatrie St. Gallen
Pfäfers Dorf, Canton of St. Gallen, 7312, Switzerland
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Psychiatrie St. Gallen
Rorschach, Canton of St. Gallen, 9400, Switzerland
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Psychiatrie St. Gallen
Sankt Gallen, Canton of St. Gallen, 9000, Switzerland
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Psychiatrie St. Gallen
Sargans, Canton of St. Gallen, 7320, Switzerland
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Psychiatrie St. Gallen
Uznach, Canton of St. Gallen, 8730, Switzerland
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Psychiatrie St. Gallen
Wattwil, Canton of St. Gallen, 9630, Switzerland
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Psychiatrie St. Gallen
Wil, Canton of St. Gallen, 9500, Switzerland
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