Awareness and Attitudes Regarding Prenatal and Preimplantation Genetic Diagnosis for Inherited Breast/Ovarian Cancer Risk
NCT ID: NCT00735150
Last Updated: 2010-10-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
34 participants
OBSERVATIONAL
2008-03-31
2010-10-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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1
25 female and 5 male BRCA carriers
questionnaire, interview
You will be asked to make a one-time visit to MSKCC. At that research visit, you will be asked to complete a short questionnaire about your knowledge of various reproductive technologies relevant to individuals at hereditary risk. Then you will watch a short presentation about these reproductive technologies and complete a second brief questionnaire to assess your understanding of the presentation. Afterwards, you will meet with an interviewer one-on-one for about one hour, during which time you may share your thoughts and feelings about the use of these reproductive technologies.
Interventions
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questionnaire, interview
You will be asked to make a one-time visit to MSKCC. At that research visit, you will be asked to complete a short questionnaire about your knowledge of various reproductive technologies relevant to individuals at hereditary risk. Then you will watch a short presentation about these reproductive technologies and complete a second brief questionnaire to assess your understanding of the presentation. Afterwards, you will meet with an interviewer one-on-one for about one hour, during which time you may share your thoughts and feelings about the use of these reproductive technologies.
Eligibility Criteria
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Inclusion Criteria
* Over age 18 and:
1. For women, less than 43
2. For men, less than 50.
* Received genetic testing and counseling for BRCA.
* Fluent in English.
Exclusion Criteria
* Individuals who refuse to discuss reproductive issues.
* Unable to give informed consent due to physical, cognitive, or psychiatric disability
18 Years
39 Years
ALL
No
Sponsors
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The New School for Social Research
OTHER
Hadassah Medical Organization
OTHER
New York University
OTHER
New York Presbyterian Hospital
OTHER
Memorial Sloan Kettering Cancer Center
OTHER
Responsible Party
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Memorial Sloan-Kettering Cancer Center
Principal Investigators
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Karen Hurley, PhD
Role: PRINCIPAL_INVESTIGATOR
Memorial Sloan Kettering Cancer Center
Locations
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Memorial Sloan-Kettering Cancer Center
New York, New York, United States
Countries
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Related Links
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Memorial Sloan-Kettering Cancer Center
Other Identifiers
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06-137
Identifier Type: -
Identifier Source: org_study_id