Clinical trial Recruiting at 1 site Interventional Ages 10 to 35

Decision aid to support choices for coronary artery anomalies

Official title: Development of a Shared Decision Aid for Anomalous Aortic Origin of a Coronary Artery

Run by Vanderbilt University Medical Center · NCT07544979 · Data updated 2026-11-12

This study tests a decision aid to help English-speaking patients 10-35 and their families weigh management options for R-AAOCA without ischemia.

Quick facts

Study typeInterventional
Ages10 Years to 35 Years
SexAll
Enrollment60 (estimated)
SponsorVanderbilt University Medical Center
Academic / other
Locations5 sites (Boston, Massachusetts and 4 other locations)
StatusRecruiting
StartedAugust 1, 2026
Main results expectedMarch 30, 2029
Study endsMarch 30, 2029
Registry record updatedAugust 11, 2026
Trial IDNCT07544979 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are English-speaking patients aged 10-35 with R-AAOCA without myocardial ischemia and their English-speaking parents/caregivers, without other significant cardiac conditions.

Probably not a fit

Patients with non-English language needs or those with additional major cardiac anomalies may not benefit from this SDM-focused tool.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This interventional study focuses on developing and testing a decision aid to support shared decision making for patients with right coronary artery anomalies originating from the left side. The tool is designed to present evidence and help align treatment choices with patient and family values. The study includes qualitative input from patients, parents, and clinicians to identify key decision factors and to assess how the aid influences discussions and confidence in choices. It is conducted across multiple pediatric and academic centers in the United States.

Why it matters

Potential benefit: If successful, the tool could reduce anxiety and improve satisfaction with the management decision by clarifying risks and options.

How similar studies have gone: Previous SDM and decision aids in cardiology have shown improvements in knowledge and satisfaction, supporting potential benefit for this application.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients

  * English-speaking
  * 10-35 years of age
  * Diagnosis of R-AAOCA without evidence of myocardial ischemia

Parents

* English-speaking
* Child 10-17 years of age
* Diagnosis of R-AAOCA without evidence of myocardial ischemia

Exclusion Criteria:

* Patients

  * Other significant cardiac anomalies
  * Unwilling or unable to provide consent
  * Non-English Speaking Parents
  * Child with other significant cardiac anomalies
  * Unwilling or unable to provide consent
  * Non-English Speaking

Where it's running

  • Vanderbilt University Medical Center
    Nashville, Tennessee, United States
    Recruiting
  • Boston Children's Hospital
    Boston, Massachusetts, United States
    Not yet recruiting
  • Children's Hospital of Philadelphia
    Philadelphia, Pennsylvania, United States
    Not yet recruiting
  • Dell Children's Medical Center
    Austin, Texas, United States
    Not yet recruiting
  • Texas Children's Hospital
    Houston, Texas, United States
    Not yet recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.