The OI Foundation Research Announcement
A new study through the OI Foundation in America, is open for biological parents with osteogenesis imperfecta (OI) and biological parents of children with OI.
This study will explore attitudes towards prenatal diagnostic testing.
Some parents may have participated in prenatal diagnostic testing with a genetic counselor during pregnancy.
It’s not necessary to have participated in any testing to take part in this research.
This study involves a self-report survey that takes most people about 20 minutes.
More details on the study and The self-report survey can be found: https://redcap.research.cchmc.org/surveys/?s=LLN8LPFYW3
Please contact Kara Ayers, Principal Investigator, at (513) 803-4402 or firstname.lastname@example.org if you have any questions.
We greatly appreciate your attention and interest in advancing research related to osteogenesis imperfecta.