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Decision Aid for Congenital Heart Disease

N/A
Recruiting
Led By Angela Fagerlin, PhD
Research Sponsored by University of Utah
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Must not have
Participants must be 18 years of age or older
Patients with other types of CHD that are not listed above are not eligible
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 week post-decision aid, 1 month post-decision, & 3 months post-decision
Awards & highlights
No Placebo-Only Group

Summary

This trial tests a web-based tool to help parents of children with serious heart conditions make better treatment decisions. The tool provides information and helps clarify what is important to the parents. Researchers will see if this tool improves parents' mental health and decision-making quality.

Who is the study for?
This trial is for parents of a fetus or neonate diagnosed with specific life-threatening congenital heart diseases (CHD), such as Truncus Arteriosus and Hypoplastic Left Heart Syndrome. Both parents are invited to participate, but one parent can join if the other cannot. Participants must be adults over 18 years old without restrictions on gender, race, or socioeconomic status.
What is being tested?
The study tests a web-based decision aid designed to help parents make informed choices about their child's CHD treatment. Some will use the decision aid alone; others will have an added values clarification exercise. Their effectiveness is compared against families making decisions without any aids.
What are the potential side effects?
Since this trial involves educational tools rather than medical treatments, there are no direct physical side effects expected from participating in the study.

Eligibility Criteria

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I am 18 years old or older.
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My heart condition is not listed as an eligible type for this trial.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 week post-decision aid, 1 month post-decision, & 3 months post-decision
This trial's timeline: 3 weeks for screening, Varies for treatment, and 1 week post-decision aid, 1 month post-decision, & 3 months post-decision for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Change in the Brief Symptom Inventory (BSI) Global Severity Index of Global Distress
Secondary study objectives
Brief Symptom Inventory (BSI) Global Severity Index of Global Distress
Decision Quality - Knowledge
Decision Quality - Values
+1 more
Other study objectives
Acceptability of the Decision Aid
Combined Outcome Measure for Risk Communication and Treatment Decision Making Effectiveness (COMRADE)
Consultation Quality
+10 more

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

3Treatment groups
Experimental Treatment
Active Control
Group I: Decision Aid & Values Clarification ExerciseExperimental Treatment2 Interventions
Participants view both the Decision Aid and the Values Clarification Exercise
Group II: Decision AidExperimental Treatment1 Intervention
Participants view the Decision Aid only
Group III: Standard Care (Control)Active Control1 Intervention
Participants will receive standard care and will not view either the Decision Aid or the Values Clarification Exercise

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for Congenital Heart Disease (CHD) include surgical interventions, catheter-based procedures, and pharmacotherapy. Surgical interventions, such as open-heart surgery, aim to correct structural defects, improving blood flow and heart function. Catheter-based procedures, like balloon angioplasty or stent placement, are minimally invasive techniques used to open narrowed vessels or repair defects. Pharmacotherapy involves medications that manage symptoms or prevent complications, such as diuretics to reduce fluid buildup or beta-blockers to control heart rate. These treatments are crucial for CHD patients as they address the underlying structural issues, improve quality of life, and reduce the risk of long-term complications. Decision aids help patients and families understand these options, facilitating informed decision-making and personalized care.
Recommendations for cardiovascular magnetic resonance and computed tomography in congenital heart disease: a consensus paper from the CMR/CCT working group of the Italian Society of Pediatric Cardiology (SICP) and the Italian College of Cardiac Radiology endorsed by the Italian Society of Medical and Interventional Radiology (SIRM) Part I.Pediatric cardiovascular safety: challenges in drug and device development and clinical application.

Find a Location

Who is running the clinical trial?

University of UtahLead Sponsor
1,139 Previous Clinical Trials
1,697,145 Total Patients Enrolled
American Heart AssociationOTHER
346 Previous Clinical Trials
4,971,318 Total Patients Enrolled
Angela Fagerlin, PhDPrincipal InvestigatorUniversity of Utah
2 Previous Clinical Trials
2,883 Total Patients Enrolled

Media Library

Decision Aid Clinical Trial Eligibility Overview. Trial Name: NCT04437069 — N/A
Congenital Heart Defects Research Study Groups: Standard Care (Control), Decision Aid, Decision Aid & Values Clarification Exercise
Congenital Heart Defects Clinical Trial 2023: Decision Aid Highlights & Side Effects. Trial Name: NCT04437069 — N/A
Decision Aid 2023 Treatment Timeline for Medical Study. Trial Name: NCT04437069 — N/A
~27 spots leftby Jun 2025