Actively Recruiting
Psychological Trauma, Post-Traumatic Stress Disorder, and Resilience in Adults With Congenital Heart Disease
Led by Dartmouth-Hitchcock Medical Center · Updated on 2026-03-25
1000
Participants Needed
3
Research Sites
47 weeks
Total Duration
On this page
Sponsors
D
Dartmouth-Hitchcock Medical Center
Lead Sponsor
A
Adult Congenital Heart Association
Collaborating Sponsor
AI-Summary
What this Trial Is About
The purpose of this study, entitled "Psychological trauma, post-traumatic stress disorder, and resilience in adults with congenital heart disease in a large population sample", is to evaluate for exposures during a lifetime with congenital heart disease that may be associated with higher likelihood of developing PTSD. Primary aim: \- Identify individual patient characteristics (medical, psychosocial, socioeconomic, etc.) that are associated with a diagnosis of PTSD. Secondary aims: * Calculate the prevalence of those meeting PTSD criteria in the ACHD population using the "gold standard" diagnostic clinician interview, while using the same data to validate a PTSD screening self-report survey in the ACHD population. * Determine the role of resilience in ACHD patients using a validated screening survey to assess its protective role toward PTSD. Hypotheses: * There are certain exposures (e.g. post-surgical pain, ICU delirium, bullying due to CHD) that are associated with a higher incidence and odds of meeting PTSD criteria. * "Gold standard" diagnostic interviews will most accurately estimate the prevalence of PTSD in ACHD which has been overestimated on prior screening-based studies, although the scope of the problem is still great. * Patients with a higher resilience score will show an association with a lower risk of PTSD.
CONDITIONS
Official Title
Psychological Trauma, Post-Traumatic Stress Disorder, and Resilience in Adults With Congenital Heart Disease
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of congenital heart disease and age 18 years or older
- Enrolled in the Congenital Heart Initiative (CHI) registry
- Able to complete surveys in English
- Access to an internet connection via computer or handheld device
You will not qualify if you...
- Opted out of the study
- Under 18 years of age
- No diagnosis of congenital heart disease
- Not enrolled in the CHI registry or unable to access the internet
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 3 locations
1
Children's National Medical Center
Washington D.C., District of Columbia, United States, 20010
Not Yet Recruiting
2
Dartmouth Hitchcock Medical Center
Lebanon, New Hampshire, United States, 03766
Actively Recruiting
3
Nationwide Children's Hospital
Columbus, Ohio, United States, 43205
Not Yet Recruiting
Research Team
D
David J Harrison, MD
CONTACT
J
Jamie Jackson, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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