Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-26 @ 4:01 PM
Ignite Modification Date: 2025-12-26 @ 4:01 PM
NCT ID: NCT07302906
Eligibility Criteria: Inclusion Criteria: * Adult patients (≥18 years) attending participating outpatient clinics at Hospital de Clínicas - Federal University of Paraná during the study period. * Receiving care from a physician who is participating in the trial. * Able to understand Portuguese and provide written informed consent for audio recording of the consultation and completion of brief questionnaires. * Able to complete the post-visit questionnaires (with assistance if needed). * Physicians (attendings or residents) working in the participating outpatient clinics. * Use the hospital electronic medical record in routine care. * Agree to have their consultations audio-recorded and to complete brief post-visit questionnaires for each included visit. Exclusion Criteria: * Patients younger than 18 years. * Emergency, urgent-care, or inpatient consultations. * Patients with significant cognitive impairment, acute distress, or clinical instability that, in the opinion of the treating physician, precludes informed consent or completion of questionnaires. * Patients under legal guardianship or otherwise unable to provide their own consent. * Consultations in which either the patient or the physician declines audio recording or participation in the study. * Consultations in which the AI system is unavailable or malfunctioning (for protocol adherence analyses only).
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Study: NCT07302906
Study Brief:
Protocol Section: NCT07302906