RightFit
RecruitingPhase not listed

Singula Phase 0.1 Primary Care Pilot

Validation of an Artificial Intelligence (AI)-Powered Clinical Decision Support System for Anxiety and Depression in Primary Care Settings

Who can join

As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.

Age
18 Years and older
Sex
All sexes
Healthy volunteers
Accepted
Compensation
Not stated

Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.

What to expect

No one can promise a trial will help you personally — that is what the research is trying to find out.

What participation involves

Not stated in the study description — ask the study team about visits and procedures.

Compensation
Not stated
  • Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
  • Participants are monitored closely by the research team throughout the study.
  • Some participants may receive access to an investigational treatment, which is still being studied.
  • Your participation helps researchers learn whether this approach could help future patients.

About this study

In plain language

This study tests a Singula Health system for adults with a routine primary care visit. Patients fill out an online survey before their visit, and the system makes a summary for their clinician that the study leader checks first. The study checks whether the summaries are made and delivered reliably, whether clinicians find them useful and acceptable, and whether patients can finish the survey and find it acceptable.

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.

Compensation is read from the study's own description and may be missing — always confirm with the study team.

Eligibility

Who can join

  • Are 18 or older when you agree to join.
  • Have a routine, non-urgent primary care visit at a participating clinic.
  • Can read and understand enough English to complete the online consent form and survey on your own.
  • Have access to a smartphone, tablet, or computer with internet to complete the survey.
  • Can understand the study and give your consent to join.

Who can't join

  • Cannot read enough English to complete the online consent form and survey on your own.
  • Have vision problems that prevent you from reading the online consent form on your own using only standard device accessibility features.
  • Cannot read for any reason, including reading difficulties or problems with thinking or memory.
  • Are having a mental health emergency or other immediate crisis that clinic staff identify at check-in.
  • Are known to be under 18 when the visit is scheduled.
  • You or your clinician choose not to take part.

Simplified for readability. The official criteria below are what the study team uses.

Official eligibility criteria

Inclusion Criteria: * 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 Criteria: * 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. * 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. * Patient is a known minor at the time of scheduling (under 18 years). * Patient or clinician declines participation.

Study sites (2)

NY