The short answer is: it depends on the type of research, what’s being studied, and how the study is
designed.
Clinical trials, which test experimental treatments or interventions, can raise legitimate ethical
concerns
when pregnant women are involved. But the Pregnancy Evidence Project isn't a clinical trial – it's an
observational study.
“Observational” means you won’t be assigned any new treatments, asked to take anything, or change your
care
in
any way. Researchers simply collect and analyze data from real experiences as they happen, so no risks are
introduced by the study itself. This type of research is how we've built much of what we do know about
medication safety and other outcomes in pregnancy today.
When you participate in observational research via the Pregnancy Evidence Project:
You're always in control. We will never give you medical advice, ask you to
change your behavior, or
assign
you to any kind of treatment. You decide what you share, and you can stop at any time.
Your identity is protected. When your responses are saved, your name is
replaced with a unique participant
ID.
Researchers access carefully prepared, de-identified data – never your individual responses.
Your data is secure. Your answers are stored in a secure, HIPAA-compliant
research database with strict
access
controls. Only authorized members of the research team can access it, and only for research purposes.
Ethics, safety & privacy are independently reviewed. The Pregnancy Evidence
Project is approved and
overseen
by an Institutional Review Board (IRB) – an independent committee of experts required by law to ensure
your
rights and well-being are protected during research.