Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06377033

Using Behavioral Economics and Implementation Science to Advance the Use of Genomic Medicine Utilizing an EHR Infrastructure Across a Diverse Health System

Led by University of Pennsylvania · Updated on 2025-07-20

1000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating new ways to deliver genomic medicine by using electronic health record (EHR) systems to support genetic testing in patients whose results can change medical management. This study evaluates clinician- and patient-directed nudges based on behavioral economics to increase the use of genetic testing across a diverse health system. The trial aims to refine patient identification algorithms and assess implementation strategies through a pragmatic randomized clinical trial involving multiple specialties and conditions. Participants include specialist clinicians randomized into six groups receiving different types of nudges: clinician nudges to order or refer for genetic testing, patient nudges via text message, combinations of both, a generic clinician alert, or usual care. The interventions use EHR tools such as Best Practice Alerts, SmartSets for ordering tests and referrals, and informational websites. Patients identified by electronic phenotype algorithms are enrolled and nudged accordingly. The trial runs over three years, monitoring genetic testing rates and implementation outcomes. Clinicians and patients participate through their routine medical visits where EHR alerts prompt actions related to genetic testing. Patient engagement includes receiving educational materials and text messages before appointments. Outcomes measured include rates of genetic testing, test orders or referrals, patient engagement, detection of genetic variants, and clinician actions. The study includes ongoing monitoring of nudge delivery and trial fidelity, with results shared through multiple dissemination platforms to support broader adoption of genomic medicine.

CONDITIONS

Brief Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years of age or older
  • Diagnosed with one of the study conditions such as Genetic Predisposition, Paraganglioma, Pheochromocytoma, ALS, Parkinson Disease, Polyneuropathies, Frontotemporal Dementia, Alzheimer Disease, Non-ischemic Cardiomyopathy, or Thoracic Aortic Aneurysm
Not Eligible

You will not qualify if you...

  • Under 18 years of age
  • Not diagnosed with one of the study conditions

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Participants are identified using electronic health record algorithms and confirmed through medical record review.

Monitoring

Duration - Up to 3 years

Participants are monitored through their routine medical care where electronic nudges are delivered to clinicians and/or patients to encourage genetic testing when appropriate.

Nudges are delivered at scheduled medical appointments; patient nudges are sent via text message within 72 hours before appointments, and clinician nudges appear during clinical visits.

Trial Site Locations

Total: 1 location

1

Penn Medicine

Philadelphia, Pennsylvania, United States, 19104

Actively Recruiting

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Research Team

B

Benita Weathers, MPH

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

FACTORIAL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

6

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Published Research Related To This Trial

Protocol for a type 3 hybrid implementation cluster randomized clinical trial to evaluate the effect of patient and clinician nudges to advance the use of genomic medicine across a diverse health system.

Anna C Raper, Benita L Weathers, Theodore G Drivas...

https://pubmed.ncbi.nlm.nih.gov/39160614