RecruitingNot ApplicableNCT07559253

Implementation of an Accessible Healthcare Model (ACHD STRONG): Comparing Nurse and Physician Lead Healthcare Transition Education in a RE-AIM Framework


Sponsor

University of Wisconsin, Madison

Enrollment

450 participants

Start Date

Dec 1, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

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.


Eligibility

Min Age: 12 YearsMax Age: 26 Years

Inclusion Criteria5

  • 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 Criteria1

  • Providers may decline participation of any patient at their clinical discretion

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

OTHERAccessible Care Model Visit

Accessible care activities will be performed by the provider following the patient participants enrollment in the study and may be observed by study staff.

OTHERRecruitment Interviews

A subset of 3-10 patient participants (plus their health care providers) who consent to be reapproached will complete 30-60 minute recruitment interviews.

OTHERParticipating Patient-Support Person Interviews

Patients, and their support person if present, may complete a 30-60 minute structured or unstructured interviews following the education session in a standard clinical encounter. Dyadic interviews will be analyzed 5 at a time over three phases of study until saturation.

OTHERParticipating Patient-Support Person Surveys

Participants will complete a survey led by the study team member to identify factors hypothesized to affect transition including age, ethnicity, race, education, transportation, distance from home to clinic, other children at home, plans for care in the transition from pediatric to adult care.

OTHERParticipating Provider Interviews and surveys

Before the end of each wave we will conduct brief (15-20 minute) unstructured interviews with the healthcare team.

OTHERUnstructured and semi-structured interviews

Semi-structured interviewing is based on the use of an interview guide. Unstructured interviewing is used both as a form of primary data collection and to develop semi-structured interview or survey questions. It is particularly useful know about the lived experience of a participant. In this case, their experiences of transition education and of the clinical encounter.


Locations(1)

University of Wisconsin

Madison, Wisconsin, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07559253


Related Trials