Heart2Heart for Teens With CHD

N/AEnrolling By InvitationNCT07764510

Kristen Fox90 enrolled

Overview

The goal of this clinical trial is to learn if teens living with congenital heart disease like and will use Heart2Heart and if it affects how they think and feel about e-cigarettes. Heart2Heart is a website that provides health information for teens with congenital heart disease. The main questions this trial aims to answer are: * Will teens enroll in the trial and complete the trial activities? * Do teens use and like Heart2Heart? * Does using Heart2Heart affect how teens think and feel about e-cigarettes? Researchers will compare the Heart2Heart group to a group that does not use Heart2Heart to see if it affects teens' thoughts and feelings about e-cigarettes. Participants will: * Complete online surveys * If assigned, explore the Heart2Heart website * If invited, share their opinions about Heart2Heart in an online discussion

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

PREVENTION

Masking

NONE

Enrollment

Conditions

Congenital Heart Disease Health Behavior

Interventions

Eligibility

Sex: ALLMin age: 12 YearsMax age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * 12-18 years of age * diagnosis of structural congenital heart disease * if under 18, has a parent or legal guardian proficient in English or Spanish Exclusion Criteria: * teen not proficient in English * teen has cognitive impairments that interfere with completion of the study activities * teen was a participant in one of the Heart2Heart development studies * teen does not have access to a device that can connect to the internet * teen is leaving the United States during their study period

Outcomes

Primary Outcomes

Percent of participants completing trial activities (Feasibility)

The following aspects of feasibility will be evaluated: recruitment rate (number enrolled/number invited), retention rate (number completing trial activities/number randomized to a group), and assessment completion rate (percent of participants completing the trial surveys).

Time frame: Feasibility will be evaluated throughout the recruitment, enrollment, and data collection process, lasting a period of three months.

Percent of participants with favorable satisfaction and usability ratings (Acceptability)

To evaluate acceptability, the percentage of teens with favorable (the highest two ratings on the scale) usability and satisfaction ratings will be calculated.

Time frame: Acceptability will be measured at the post-intervention survey, two weeks after participants are assigned to a study group.