IMProving Executive function Study (IMPRES)

  • STATUS
    Recruiting
  • participants needed
    100
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Updated on 19 February 2024

Summary

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.

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.

FAQ

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: https://www.med.upenn.edu/penn-promotes/pcwbw-impres.html

Details
Condition Ovarian cancer,BRCA mutation carriers,MENOPAUSE
Age 35years - 58years
Clinical Study IdentifierTX4818
Last Modified on19 February 2024

Eligibility

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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