Enrolling by invitation NCT07497633

Spontaneous Coronary Artery Dissection (SCAD) Avatar Study

— Observational Spontaneous Coronary Artery Dissection

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied: The protocol lists: Video Avatar Interview, Voice-Only Avatar Interview, Human Interview.
Who it may be relevant to: Registry conditions: Spontaneous Coronary Artery Dissection. Basic parameters: 18 years — 99 years · All.
What needs checking: Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place: United States
Next step: Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Spontaneous Coronary Artery Dissection (SCAD) Avatar Study (Pilot)

Overview

The purpose of this study is to evaluate patient satisfaction, comfort, and trust in interacting with an avatar compared with speaking to a human clinician during a pre clinical visit.

Interventions

Other Video Avatar Interview
Patients will undergo a pre-visit interview with a Video Avatar (LLM powered digital interviewer presented with on-screen video)
Other Voice-Only Avatar Interview
Patients will undergo a pre-visit interview with a Voice-Only Avatar ( LLM-powered interviewer delivered without visuals)
Other Human Interview
Patients will undergo a Human Interview conducted by trained Mayo personnel

Primary outcome measures

Patient Satisfaction [Time frame: Baseline]

Eligibility criteria

Inclusion criteria

All patients scheduled for a SCAD appointment at Mayo Clinic

Exclusion criteria

Not Applicable

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model: Cohort

Study locations

United States · 1 center

Mayo Clinic — Rochester

Identifiers

NCT: NCT07497633 · 25-014040

Primary sources (government registries)

ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗