Condition: Adult Congenital Heart Disease · Congenital Heart Disease · PTSD · Sponsor: Dartmouth-Hitchcock Medical Center
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.
This description comes directly from the study's public registry record.
David J Harrison, MD · 603-650-5724 · david.j.harrison@hitchcock.org
Jamie Jackson, PhD · jamie.jackson2@nationwidechildrens.org
Always discuss trial participation with your own doctor first.
| Children's National Medical Center | Washington D.C., District of Columbia, United States | Not Yet Recruiting |
| Dartmouth Hitchcock Medical Center | Lebanon, New Hampshire, United States | Recruiting |
| Nationwide Children's Hospital | Columbus, Ohio, United States | Not Yet Recruiting |
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Source record: clinicaltrials.gov/study/NCT06952933