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Noninvasive Prenatal Testing

NCT02586428 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 33

Last updated 2016-10-14

No results posted yet for this study

Summary

Before and after a patient receives genetic counseling they will be offered the chance to complete the survey, by their counselor. Since each patient sees only one genetic counselor that counselor will be responsible for consenting and giving and collecting the finish surveys. No identifiers will be used. The investigators will emphasize that their answers will remain anonymous throughout the entire process, and that their participation is strictly voluntary. The patient will be provided with a survey and asked to complete this before their genetic counseling session and after.The survey will be returned to the genetic counselor and placed in a locked drawer. Information will also be collected from the medical record including age, pregnancy history and the reason for the visit.

Conditions

  • Genetic Counseling

Interventions

OTHER

what patients elect noninvasive prenatal testing (NIPT)

what percentages of patients elect noninvasive prenatal testing (NIPT), amniocentesis, or no testing before and after genetic counseling.

Sponsors & Collaborators

  • St. Louis University

    lead OTHER

Principal Investigators

  • Gary Fruhman, MD · St. Louis University

Eligibility

Min Age
14 Years
Max Age
55 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-09-30
Primary Completion
2016-04-30
Completion
2016-04-30

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 NCT02586428 on ClinicalTrials.gov