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The Value of Genetic Information to Adult Adopted Individuals

NCT00057694 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 40

Last updated 2008-03-04

No results posted yet for this study

Summary

This study will explore adult adoptees' perceptions of the potential value of genetic and family history information. Unlike most people, many adopted individuals do not have access to personal or family medical information because of laws and practices that prevent disclosure. Research suggests that adopted individuals are interested in obtaining this information about their biological families. This study will examine adoptees':

* Satisfaction with the amount of genetic information they have, their motivations for wanting more information, and when it becomes important for them to have this information.
* Perceptions of the degree to which they believe genetics and family history influence various traits and conditions.

The study will also explore adoptees' interactions with health care providers so that recommendations can be developed for helping genetic counselors meet the needs of these individuals.

English-speaking adoptees 18 years of age and older are eligible for this study. Those enrolled will participate in a one-time telephone interview that will take about 45 to 60 minutes. The interview will obtain demographic information, such as the adoptee's age, sex, racial and ethnic background, marital status, and education level, and will include questions in the following areas:

* Personal adoption story;
* Perceptions of the role of the biological family history and medical information and its importance and usefulness;
* Perceptions of the influence of genetics and family history on health;
* Reproductive history and pregnancy concerns related to being adopted;
* Experiences and interactions with health care providers related to adoption;
* Suggestions for improving interactions with health care providers.

Conditions

  • Adoption
  • Genetic Counseling

Sponsors & Collaborators

  • National Human Genome Research Institute (NHGRI)

    lead NIH

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2003-04-30
Completion
2004-01-31

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 NCT00057694 on ClinicalTrials.gov