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NCT07525843 · ClinicalTrials.gov registry record · NA

A Pragmatic Clinical Trial of the WE BEAT Well-Being Education Program in Adolescent Congenital Heart Disease: WE BEAT CHD Study

A NA study, sponsored by Carelon Research.

Recruiting
Registry status
NA
Development phase
390
Enrollment target

NCT07525843 is a NA study that is actively recruiting participants, run by Carelon Research. The registered enrollment target is 390 participants.

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The verdict

NCT07525843, a NA study, is actively recruiting participants, sponsored by Carelon Research.

RECRUITING
Registry status
NA
Development phase
390 participants
Enrollment target

Study Summary

The goal of this pragmatic clinical trial is to learn if the WE BEAT program, a 5-week group-based online wellbeing and skill-building program, can help teens with congenital heart disease (CHD) improve their ability to handle stress. The main question it aims to answer is if participants who receive the WE BEAT program become more resilient (the ability to bounce back from from tough times or recover from something difficult) and have better quality of life compared to participants who receive usual care. The study also aims to learn if there are connections between participant-reported psychosocial data (such as resilience, feelings about one's life and one's physical, mental, and social wellbeing) and clinical outcomes. Eligible participants who are 12-17-year-old will be in the study for about 6 months and be randomized to receive either the WE BEAT program or usual care. Following completion of the primary WE BEAT intervention at Week 5, intervention arm participants will be randomized to a single-session booster session (occurring at Week 18) vs no booster session. The booster session will be provided in a similar format to the WE BEAT program. A review of all modules/skills introduced in the program will be provided. All participants will complete 4 sets of online surveys and give 3 hair/saliva samples at different timepoints. Some participants may volunteer to give optional blood and urine samples.

Interventions

  • BEHAVIORAL Telemedicine-based resiliency-building intervention

Trial Details

FieldValue
Enrollment Target 390 participants
Start Date 2026-04-20
Est. Completion 2029-06
Phase NA

Sponsor

Carelon Research

50 total trials

What the Registry Record Tells You About NCT07525843

The ClinicalTrials.gov registry entry for NCT07525843 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 390 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Carelon Research, which has 50 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Telemedicine-based resiliency-building intervention is the first listed.

NCT07525843 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT07525843 about?

NCT07525843 is a clinical study titled "A Pragmatic Clinical Trial of the WE BEAT Well-Being Education Program in Adolescent Congenital Heart Disease: WE BEAT CHD Study". The goal of this pragmatic clinical trial is to learn if the WE BEAT program, a 5-week group-based online wellbeing and skill-building program, can help teens with congenital heart disease (CHD) improve their ability to handle stress. The main question it aims to answer is if participants who receiv...

What is the current status of trial NCT07525843?

This trial is currently recruiting. It is a NA study. The enrollment target is 390 participants. The study started on 2026-04-20. Estimated completion is 2029-06.

What interventions are being tested in trial NCT07525843?

The interventions under investigation include: Telemedicine-based resiliency-building intervention (BEHAVIORAL).

Who is sponsoring clinical trial NCT07525843?

This trial is sponsored by Carelon Research, which has 50 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.