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N/A Completed N=78 Randomized Triple-blind Treatment

Assessing and Promoting Resilience in Patients With Adult Congenital Heart Disease

Source: ClinicalTrials.gov NCT04738474 ↗
Enrolled (actual)
78
Serious AEs
0.0%
Results posted
Oct 2025
Primary outcomePrimary: Feasibility of Enrollment — 40; 38 Participants

Summary

The purpose of this study is to evaluate the feasibility and preliminary efficacy of the Promoting Resilience in Stress Management (PRISM) intervention in patients with adult congenital heart disease.

Outcome Measures

OutcomeResultp-value
PRIMARY
Feasibility of Enrollment
40; 38
PRIMARY
Feasibility of PRISM
32; 35
SECONDARY
Mean Resilience
30.1; 28.7

Eligibility Criteria

Inclusion Criteria

  • adults with moderate or complex ACHD, stages B, C, or D as defined by the 2018 ACHD guidelines
  • receive care in our health system

Exclusion Criteria

  • diagnosis of another life-limiting illness
  • inability to participate in study activities independently and in English
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04738474). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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