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Family Health After Predictive Huntington Disease (HD) Testing

NCT00075140 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 422

Last updated 2009-01-16

No results posted yet for this study

Summary

The purpose of this study is to identify health management concerns and needs of family members of asymptomatic and symptomatic persons with mutation in the gene for Huntington Disease (HD).

Conditions

  • Huntington Disease

Interventions

GENETIC

Mutation in the gene

Sponsors & Collaborators

  • National Institute of Nursing Research (NINR)

    lead NIH

Principal Investigators

  • Janet K Williams, PhD, RN, FAAN · University of Iowa

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2001-09-30
Primary Completion
2008-10-31
Completion
2008-10-31

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 NCT00075140 on ClinicalTrials.gov