Participate In Research To Help Women With A History Of Physical Or Sexual Assault/Abuse

Updated on 25 March 2021


Participate In Research To Help Women With A History Of Physical Or Sexual Assault/Abuse


Research in the Stress, Trauma, and Recovery Research Center (STARRC) within the Department of Psychology at the University of Kentucky are seeking adult women to participate in an ongoing research study.
This study, which will involve 2 visits to the laboratory and a two-week period of brief, daily assessments, is focused on understanding emotional experiences among women with histories of physical or sexual assault/abuse.
The long-term goal of this study is to enhance treatments for women with difficulties related to experiences involving physical or sexual assault/abuse. For more information about the Women’s Trauma or Emotion Study, contact:

Stress, Trauma, and Recovery Research Center (STARRC)

Condition Women's Health
Clinical Study IdentifierTX147029
Last Modified on25 March 2021


Yes No Not Sure

Inclusion Criteria

You may be eligible to participate if you
Are female
Are over the age of 18; and
Have experienced one or more of the following at any time during your life
Physical abuse or assault
Sexual abuse, rape, attempted rape, or any other unwanted or coercive sexual experience
Participants will be compensated upto $160
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

You are contacting

Investigator Avatar

Primary Contact


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

Learn more

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.

Learn more

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

Learn more

Similar trials to consider


Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer

user name

Added by • 



Reply by • Private

Lorem ipsum dolor sit amet consectetur, adipisicing elit. Ipsa vel nobis alias. Quae eveniet velit voluptate quo doloribus maxime et dicta in sequi, corporis quod. Ea, dolor eius? Dolore, vel!

  The passcode will expire in None.

No annotations made yet

Add a private note
  • abc Select a piece of text from the left.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.
Add a private note