Postpartum depression: Research Studies

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Be an Informed Participant

Before deciding to participate in a research study, take time to learn about clinical research, how it's conducted and your rights as a research participant. Following are some helpful resources from independent sources. Always remember that a clinical research study is research, not treatment.

Know Who to Contact

Eligibility: For questions about a specific study and who is eligible to participate, call or email the contact person listed for that study.
Your Rights: For questions about your rights as a research participant, contact the UF Institutional Review Boards at 352-273-9600.
Feedback: For general questions or feedback about study listings, email the UF Clinical and Translational Science Institute at UFStudies@health.ufl.edu.

Other Resources

ResearchMatch.org: Join a national registry of volunteers willing to be contacted about research studies.

For Research Teams

Submit requests to add, update or remove study listings via the UF Clinical and Translational Science Institute.

1 Related Result(s)

A focus group study to explore the feasibility of a mHealth application to monitor and manage anxiety and mood symptoms of women during their pregnancy and postpartum period

The purpose of this research study is to assess the feasibility and acceptance of a mobile phone-based (mHealth) application to assess anxiety and mood...

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Studies listed on this site have been approved by a UF Institutional Review Board (IRB), which works to ensure the welfare and rights of research participants as required by federal regulations. Study listings are provided by the UF Clinical and Translational Science Institute in collaboration with UF research teams and the UF IRBs.