Startle Response in Women with Premenstrual Mood Disorders

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Updated on 19 February 2024

Summary

This study examines stress response in women with premenstrual mood changes. For this study, you will be asked to fill out forms about your physical and mental health, have blood and saliva samples taken, and undergo a test that will measure your stress responses. This is a long-term study, consisting of 4 visits over the course of about 4 months. Compensation will be provided for your time.

Description

For this study, you will be asked to fill out forms about your physical and mental health, have blood and saliva samples taken, and undergo a test that will measure your stress responses. This is a long-term study, consisting of 4 visits over the course of about 4 months. Compensation will be provided for your time.

FAQ

You may qualify for this study if you are: - A woman; Between 18-50 years old; NOT taking hormonal birth control pills; NOT on medication for depression, anxiety, pain, or sleep disorders. Please contact the study team directly for more information and to determine eligibility.

Details
Condition Premenstrual syndrome, Mood Disorders, healthy Volunteers, healthy subjects, Healthy, healthy controls, Women, Women's Health, Healthy Control, Healthy volunteer, Premenstrual, healthy, healthy volunteer, healthy volunteers, healthy subjects, healthy, healthy controls, healthy controls
Age 18years - 50years
Clinical Study IdentifierTX1050
Last Modified on19 February 2024

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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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