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Aim 3: Pilot Study of a Serious Game to Promote Transition Readiness Skills

Utah System of Higher Education (USHE) logo

Utah System of Higher Education (USHE)

Status

Enrolling

Conditions

Patient Centered Care
Transition-age Youth
Serious Games
Congenital Heart Disease in Adolescence
Transition to Adult Care
Congenital Heart Defect

Treatments

Behavioral: Serious game for transition readiness

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT07042334
1K12TR004413 (U.S. NIH Grant/Contract)
23SCEFIA1154397 (Other Grant/Funding Number)
IRB_00179379

Details and patient eligibility

About

This study involves testing a new video game designed to support adolescents with congenital heart disease (CHD) in preparing to manage their health independently. The game aims to teach essential skills such as communicating with healthcare providers, understanding medical information, and managing appointments and medications. This small pilot study will evaluate the game's usability, acceptability, and its impact on participants' confidence and preparedness for managing their heart care. Feedback will be collected from adolescent participants, their parents, and healthcare providers, and the study will examine how the game influences communication during clinical visits.

Enrollment

150 estimated patients

Sex

All

Ages

12+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

- Patient with congenital heart disease, their parent, and their clinician

Exclusion criteria

-Significant visual or cognitive impairment that would impede their ability to play the game and/or complete the study.

Trial design

Primary purpose

Health Services Research

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

150 participants in 1 patient group

Serious Game
Experimental group
Description:
Receive serious game to build transition readiness skills
Treatment:
Behavioral: Serious game for transition readiness

Trial contacts and locations

1

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Central trial contact

Rebecca Delaney, PhD

Data sourced from clinicaltrials.gov

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