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Parenting After Infant Congenital Heart Defect Diagnosis

NCT01503307 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 23

Last updated 2019-10-25

No results posted yet for this study

Summary

The purpose of this research study is to learn about parents' experiences following diagnosis of a fetal/neonatal Congenital Heart Defect (CHD). Nurses, physicians, and other health-care clinicians will benefit from an improved understanding of what the diagnosis means to parents and what they expect concerning the infant, being a parent, and caregiving tasks and responsibilities. The investigators expect that the knowledge gained will increase clinicians' ability to respond to parents' needs.

Conditions

  • Congenital Heart Disease

Sponsors & Collaborators

  • Children's Hospital and Health System Foundation, Wisconsin

    collaborator OTHER

  • University of Wisconsin, Madison

    collaborator OTHER

  • University of Minnesota

    collaborator OTHER

  • Medical College of Wisconsin

    lead OTHER

Principal Investigators

  • Karen Pridham, PhD, RN · University of Wisconsin, Madison

  • Anne C McKechnie, PhD, RN · University of Wisconsin, Madison

Eligibility

Max Age
12 Weeks
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-01-31
Primary Completion
2016-07-31
Completion
2016-07-31

Countries

  • United States

Study Locations

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Entities

Companies

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 NCT01503307 on ClinicalTrials.gov