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NCT00339924 · ClinicalTrials.gov registry record

Physicians' Understanding of Human Genetic Variation

A clinical trial, sponsored by National Human Genome Research Institute (NHGRI).

Completed
Registry status
1,258
Enrollment target

NCT00339924 is a clinical trial that has completed, run by National Human Genome Research Institute (NHGRI). The registered enrollment target is 1,258 participants.

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The verdict

NCT00339924 has completed, sponsored by National Human Genome Research Institute (NHGRI).

COMPLETED
Registry status
1,258 participants
Enrollment target

Study Summary

This study will develop a survey instrument to measure primary care physicians' knowledge of the variation in human genetics, their beliefs about biologic and genetic differences according to patients' race and ethnicity, and how that knowledge is used in their clinical decision making. Genomics research today is such that primary care physicians will be responsible for translating new genetic knowledge, drug therapies, and single and multiplex genetic testing into clinical practice. Physicians who are board certified general internists, including those who practice and teach in research and teaching hospitals in urban areas of the United States, may be eligible for this study. Participants will be recruited through invitation and information letters mailed to leaders of local chapters of physician organizations, through letters and e-mail sent to qualifying general internists in databases, and through e-mail sent to academic physicians who practice or teach medicine at medical schools that meet the inclusion criteria. The number of participants is estimated at 96 in the first phase of the study. The researchers are especially interested in general internists who provide general and preventative health care services to patients of various racial, ethnic, and ancestral backgrounds. This study will use qualitative methods-focus groups and semistructured interviews-and quantitative methods. Two pilot focus group sessions, with about eight members each, are planned for Washington, D.C. Other settings for the study are Atlanta, Detroit, Los Angeles, and Philadelphia. Those locations were selected based on population density, availability of several teaching hospitals with diverse patient populations, availability of physicians meeting the study requirements, and the need to address important regions nationwide. The focus groups will be separated by region and self-identified race-for example, one group consisting of African American internists from Atlanta and another

Trial Details

FieldValue
Enrollment Target 1,258 participants
Start Date 2005-07-11
Est. Completion 2012-04-13

What the Registry Record Tells You About NCT00339924

The ClinicalTrials.gov registry entry for NCT00339924 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 1,258 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is National Human Genome Research Institute (NHGRI), which has 185 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 0 interventions.

NCT00339924 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00339924 about?

NCT00339924 is a clinical study titled "Physicians' Understanding of Human Genetic Variation". This study will develop a survey instrument to measure primary care physicians' knowledge of the variation in human genetics, their beliefs about biologic and genetic differences according to patients' race and ethnicity, and how that knowledge is used in their clinical decision making. Genomics re...

What is the current status of trial NCT00339924?

This trial is currently completed. The enrollment target is 1,258 participants. The study started on 2005-07-11. Estimated completion is 2012-04-13.

Who is sponsoring clinical trial NCT00339924?

This trial is sponsored by National Human Genome Research Institute (NHGRI), which has 185 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

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