Improving Executive Function Study (Impres)

Brief Description Of Study

Dr. Neill Epperson and her study team at the Penn Center for Women's Behavioral Wellness are seeking women to help understand the effects of a stimulant medication on memory and attention in women who underwent surgically induced menopause.

Detailed Study Description

Study participation involves 3 functional brain-imaging scans (MRI), cognitive testing, and a one-time blood draw. Participants will be compensated for their time.

Additional Information About The Study

You may qualify for this study if you are: -A female, aged 35 to 58 with executive functioning complaints -Undergone risk-reducing bilateral salpingo-oophorectomy (RRSO) within the previous 15 years AND were premenstrual at the time of RRSO. -The onset of your executive functioning difficulties were post-RRSO. Please contact the study team to determine eligibility or see the study's website for more information:

Clinical Study Identifier: TX4818

Contact research investigator to learn more about this study by filling out the form below.

To: Research Study Investigator
Subject: I am interested in participating in your Research Study
Dear Investigator,
I'm interested in learning more about and participating in your research study named: IMProving Executive function Study (IMPRES)
I am hoping to hear back from you and discuss details of the study

By clicking "Contact Research Team", your contact information will be sent directly to the research staff associated with the study. You will also receive a copy of this email in your inbox, as well as other notifications to determine your participation status in the study.