# Using the EHR to Advance Genomic Medicine Across a Diverse Health System

> **NCT06377033** · NA · RECRUITING · sponsor: **University of Pennsylvania** · enrollment: 1000 (estimated)

## Conditions studied

- Genetic Predisposition
- Paraganglioma
- Pheochromocytoma
- ALS
- Parkinson Disease
- Polyneuropathies
- Frontotemporal Dementia
- Alzheimer Disease
- Cardiomyopathy Non-ischemic
- Thoracic Aortic Aneurysm

## Interventions

- **BEHAVIORAL:** Behavioral nudge

## Key facts

- **NCT ID:** NCT06377033
- **Lead sponsor:** University of Pennsylvania
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** RECRUITING
- **Start date:** 2024-06-10
- **Primary completion:** 2027-06-30
- **Final completion:** 2027-06-30
- **Target enrollment:** 1000 (ESTIMATED)
- **Last updated:** 2025-07-20


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT06377033

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT06377033, "Using the EHR to Advance Genomic Medicine Across a Diverse Health System". Retrieved via AI Analytics 2026-06-24 from https://api.ai-analytics.org/clinical/NCT06377033. Licensed CC0.

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*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*
