ProActive Athlete Heart Program: Proposal for Cardiac Risk Screening in Former High-Intensity Athletes
1 other identifier
interventional
100
1 country
1
Brief Summary
AI-Guided Coronary CT Angiography Screening in Former High-Intensity Athletes
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Aug 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 27, 2026
CompletedFirst Posted
Study publicly available on registry
March 10, 2026
CompletedStudy Start
First participant enrolled
August 28, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
January 31, 2027
Study Completion
Last participant's last visit for all outcomes
January 31, 2027
May 5, 2026
April 1, 2026
5 months
February 27, 2026
April 30, 2026
Conditions
Outcome Measures
Primary Outcomes (2)
Prevalence of Coronary Atherosclerosis
The primary outcome is to determine the prevalence of coronary atherosclerosis in former high-intensity athletes using AI-guided software to analyze a CCTA.
At CCTA assessment
Coronary Atherosclerosis Characteristics
Determine the characteristics (burden, composition, risk features) of coronary atherosclerosis in former high-intensity athletes using AI-guided software to analyze a CCTA.
At CCTA Assessment
Secondary Outcomes (1)
Plaque Burden
Day of CCTA and biomarker collection
Study Arms (1)
Athletes
EXPERIMENTALThis arm will have answer a questionnaire, have a physical exam performed as well as a Coronary CTA and labs completed. The Coronary CTA images will be analyzed using AI-software to assess plaque quantification and an ischemia analysis.
Interventions
The Coronary CTA will be performed for each participant. These images will be analyzed using AI-software to assess plaque quantification and an ischemia analysis, if necessary.
Eligibility Criteria
You may qualify if:
- Former professional or collegiate high-intensity athletes (e.g., NFL alumni, Division I athletes, or equivalent competitive-level participants).
- Age ≥30 years
You may not qualify if:
- eGFR \<40 mL/min/1.73 m²
- Known iodinated contrast allergy
- Weight \>450 lbs. (scanner table limit)
- Inability to hold breath \>10 seconds
- Uncontrolled arrhythmia
- Contraindication to beta-blocker, Calcium Channel Blockers and nitroglycerin
- Taking part in another research study that has not given their permission to participate in this one
- Pregnancy
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Baylor Research Institutelead
- Cleerly, Inc.collaborator
Study Sites (1)
Baylor Scott & White The Heart Hospital- Plano
Plano, Texas, 75093, United States
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- SCREENING
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 27, 2026
First Posted
March 10, 2026
Study Start (Estimated)
August 28, 2026
Primary Completion (Estimated)
January 31, 2027
Study Completion (Estimated)
January 31, 2027
Last Updated
May 5, 2026
Record last verified: 2026-04