Noninvasive Prenatal Testing
Stopped early
Conditions studied: Genetic Counseling
In brief
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.
Key facts
- Study ID
- NCT02586428
- Run by
- St. Louis University
- People needed
- 33
- Starts
- 2015-09-01
- Expected to finish
- 2016-04-01
- Last updated by the study team
- 2016-10-14
Who can join
Age: 14 and older, up to 55. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- high risk pregnant women seen for genetic counseling
You may not qualify if…
- low risk
- not pregnant
Where it is running
- St. Mary's Hospital — St Louis, Missouri, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.