Testing an AI tool that summarizes patient questionnaires for primary care doctors
Tests an AI tool sharing questionnaire summaries with doctors, in adults with depression or anxiety.
Plain-language title generated from the registry record
Registry title: Singula Phase 0.1 Primary Care Pilot
Key facts
- Where
- Brentwood and Mount Kisco, United StatesSee the 2 sites
Where in United States
- Morris Medical OfficeBrentwood, United StatesNo longer taking part
- WestDocs ConciergeMount Kisco, United StatesTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Singula Health, Inc.
- Trial code
- NCT07834684
- Record updated
- 22 September 2026
- Original description
This prospective, single-arm, observational pilot study evaluates a clinical decision support system developed by Singula Health for use in primary care. Adult patients complete a self-report assessment before a routine primary care visit. The system uses the responses to generate a clinician-facing Companion Brief that summarizes relevant information for the treating clinician. Each Companion Brief is reviewed by the Principal Investigator before it is provided to the clinician. The study will evaluate whether the system can reliably generate and deliver the Companion Briefs, whether clinicians find the Briefs useful and acceptable, and whether patients can successfully complete and accept the pre-visit assessment.Read full original descriptionShow less
Validation of an Artificial Intelligence (AI)-Powered Clinical Decision Support System for Anxiety and Depression in Primary Care Settings
This prospective, single-arm, observational pilot study evaluates a clinical decision support system developed by Singula Health for use in primary care. Adult patients complete a self-report assessment before a routine primary care visit. The system uses the responses to generate a clinician-facing Companion Brief that summarizes relevant information for the treating clinician. Each Companion Brief is reviewed by the Principal Investigator before it is provided to the clinician. The study will evaluate whether the system can reliably generate and deliver the Companion Briefs, whether clinicians find the Briefs useful and acceptable, and whether patients can successfully complete and accept the pre-visit assessment.
Inclusion: Adult, aged 18 years or older at the time of consent; Scheduled for a routine, non-urgent primary care visit at a participating practice; Able to read and understand English at a level sufficient to complete the electronic informed consent and Survey 0.1 independently; Has personal-device access to complete the survey (smartphone, tablet, or computer with internet); Capable of providing informed consent.
Exclusion: Unable to read for any reason (literacy, cognitive impairment, or other); Presenting with an acute psychiatric emergency or in acute crisis at the time of the scheduled visit, as identified by clinic staff during routine check-in; Non-English-speaking, defined as inability to read English at a level sufficient to complete electronic informed consent and the survey independently; Visually impaired to a degree that prevents independent reading of an electronic consent form on a personal device, without specialized assistive technology beyond standard mobile-device accessibility features; Patient is a known minor at the time of scheduling (under 18 years); Patient or clinician declines participation.