Actively Recruiting

Age: 18Years +
All Genders
NCT06952933

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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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

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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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