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Patient-Reported Outcomes in Adults With Congenital Heart Disease

NCT02150603 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 4000

Last updated 2015-03-12

No results posted yet for this study

Summary

The purpose of this study is to examine the differences in perceived health, psychosocial functioning, behavioral outcomes and quality of life of adults with congenital heart disease who are living in different areas of the world, and how these differences can be understood (e.g., differences in sense of coherence or illness perceptions).

Conditions

  • Heart Defects, Congenital

Sponsors & Collaborators

  • Philip Moons

    lead OTHER

Principal Investigators

  • Philip Moons, PhD · KU Leuven

  • Koen Luyckx, PhD · KU Leuven

  • Adrienne Kovacs, PhD · Peter Munk Cardiac Centre, University Health Network

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-04-30
Primary Completion
2015-02-28
Completion
2015-02-28

Countries

  • United States
  • Argentina
  • Australia
  • Belgium
  • Canada
  • France
  • India
  • Italy
  • Japan
  • Malta
  • Netherlands
  • Norway
  • Sweden
  • Switzerland
  • Taiwan

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 NCT02150603 on ClinicalTrials.gov