Thank you for clicking the link to our survey! The survey should take about 25 minutes to complete and can be accessed with the link below. We are particularly interested in understanding your prenatal expectations and goals and post-delivery reality.

 

You are eligible to participate in this survey study if you are currently pregnant, have been told that your current pregnancy has a high risk of being complicated by placenta accreta spectrum disorder and you have not yet delivered your baby.  In addition, you must be at least 18 years of age and residing in the United States.

 

Your participation is completely voluntary, and you may stop this study at any time. Your responses will be linked to your email address but privacy will be maintained by assigning a nonspecific number ID to each linked prenatal and postpartum completed survey set. We will take extreme care to protect the privacy and security of your information. The results of this study may be published, but you will not be identified in any publication. There is no scheduled date on which your data used for this study will be destroyed. Although not of direct benefit to you, results from this study may benefit patients in the future.    

 

Responding to the survey will indicate your consent to participate in this study and for us to contact you at a scheduled time following your delivery via email, approximately 6-12 weeks after your estimated due date. If you choose to withdraw from this study, you may do so at any time.

 

Some of the questions we will ask as part of this study may make you feel uncomfortable.  You may refuse to answer any of the questions and you may take a break at any time during the study.  You may stop your participation in the study at any time. If you need additional support, please reach out to your health care provider or to the following resources:

 

National Maternal Mental Health Hotline:

https://mchb.hrsa.gov/national-maternal-mental-health-hotline

 

Postpartum International Helpline:

https://www.postpartum.net/get-help/psi-helpline/?gclid=Cj0KCQjwiIOmBhDjARIsAP6YhSX9d2N6gsf4zrrUaiQbhrGRp_2hvnEb0fuOL7KwO4S-dCPvfFBuN2EaAlykEALw_wcB

If you have questions or concerns, please contact the Principal Investigator, Dr. Scott A. Shainker, or the research assistant at placenta@caregroup.harvard.edu or 617-667-0881. You may also contact the Human Subjects Protection Office at Beth Israel Deaconess Medical Center (617-975-8500) with questions regarding your rights as a study participant.  

 

Thank you for your participation!  

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