Implementation of an Accessible Healthcare Model (ACHD STRONG): Comparing Nurse and Physician Lead Healthcare Transition Education in a RE-AIM Framework
Recruiting
N/AInterventional Study
Congenital Heart Disease
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
12 – 26
Sex
Any
Study type
Interventional
Purpose
Health Services Research
Participants needed
450 (estimated)
Sponsor
University of Wisconsin, Madison · Other
Who this trial is looking for
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The study includes patients with congenital heart disease (CHD), as well as their support persons and their providers, who are preparing to make the transition from pediatric to adult care for their CHD. The purpose of this study is to improve the tools available to help find doctors as patients enter adulthood. 200 people with CHD and support people will be enrolled.
Trial Locations
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Eligibility Criteria
Inclusion Criteria (Patient Participants):
* Diagnosed CHD patients between the ages of 12-26 will be eligible
* Able to provide assent when seen by a pediatric or adult congenital cardiologist provider.
* A subset of patients will self-identify as having a disability, and or, be identified with di…
Inclusion Criteria (Patient Participants):
* Diagnosed CHD patients between the ages of 12-26 will be eligible
* Able to provide assent when seen by a pediatric or adult congenital cardiologist provider.
* A subset of patients will self-identify as having a disability, and or, be identified with disabilities in their medical or educational records.
* Participants to provide assent/consent and complete all study activities in English or Spanish
* Participants under the age of 18 must have a legal guardian who is able to provide consent in English or Spanish.
Exclusion Criteria:
* Providers may decline participation of any patient at their clinical discretion
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