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An Evaluation of Routine Developmental Follow-Up in Infants and Children With Congenital Heart Disease

NCT01567579 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 928

Last updated 2021-11-30

No results posted yet for this study

Summary

The purpose of this study is to understand how having a heart problem affects development,quality of life, and family life in young children and their families. Results for children and families with heart disease will be compared to children and families without heart disease. The investigators hope that this information may help us to support children and families better in the future. All children and families that are seen in the HHC Developmental Follow-Up Program will be asked if they would like to take part in this study. It is hypothesized that children with congenital heart disease will demonstrate developmental delays when compared to normative values.

Conditions

  • Congenital Heart Defects

Sponsors & Collaborators

  • Children's Hospital and Health System Foundation, Wisconsin

    collaborator OTHER

  • Medical College of Wisconsin

    lead OTHER

Principal Investigators

  • Cheryl L Brosig, PhD · Medical College of Wisconsin

  • Laurel M Bear, MD · Medical College of Wisconsin

Eligibility

Min Age
6 Months
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-09-30
Primary Completion
2021-09-30
Completion
2021-09-30

Countries

  • United States

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 NCT01567579 on ClinicalTrials.gov