Assessment of Patterns of Patient Reported Outcomes in Adults With Congenital Heart Disease - International Study II

NCT04902768 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 8415

Last updated 2024-05-16

No results posted yet for this study

Summary

This is an international, cross-sectional and descriptive study that aims to investigate differences in patient-reported outcome measures (PROMs) and patient-reported experience measures (PREMs) and that aims to explore the profile and healthcare needs of adults with congenital heart diseases.

Conditions

  • Congenital Heart Disease

Interventions

OTHER

This is an observational study, there is no intervention

This is an observational study, there is no intervention. Hence, this is not applicable.

Sponsors & Collaborators

  • KU Leuven

    lead OTHER

Principal Investigators

  • Philip Moons, PhD, RN · Professor in Healthcare Sciences

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-08-01
Primary Completion
2022-08-31
Completion
2022-12-31

Countries

  • United States
  • Argentina
  • Australia
  • Austria
  • Belgium
  • Botswana
  • Brazil
  • Bulgaria
  • Cameroon
  • Canada
  • Chile
  • Colombia
  • Denmark
  • Ethiopia
  • France
  • Greece
  • India
  • Italy
  • Japan
  • Malaysia
  • Malta
  • Netherlands
  • Norway
  • Pakistan
  • Portugal
  • Senegal
  • South Korea
  • Sweden
  • Switzerland
  • Taiwan
  • Turkey (Türkiye)
  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04902768 on ClinicalTrials.gov