Research Registry
Studies and Clinical Trials
Find ongoing studies and clinical trials. Take a chance to learn about opportunities in which you may wish to participate.
We offer this registry as a complimentary service to facilitate connections between scientists and patients. All studies listed have Ethics Board Approval.
Current Studies and Trials
Please note that IAPMD cannot answer any specific requests about the below studies. Please contact the researcher and/or establishment directly.
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The purpose of the study is to better understand how people suffering from PMDD, PMS and people who do not suffer from premenstrual symptoms differ in terms of emotional regulation and how this affects interpersonal conflicts in romantic and occupational relationships during the luteal phase. A clearer understanding could inform the future development of psychological treatment interventions.
Who can participate?
Ages between 18 and 40
Based in Canada or the US
Have typical menstrual cycles
No psychotic or bipolar disorder
Not using hormonal birth control
Not pregnant or breastfeeding
What will it involve?
Complete a daily 5 minute survey for two months
Complete 3 additional surveys per cycle
Complete a zoom interview (optional)
Whom can I contact?
Stephanie Racine Maurice (PhD Candidate) OR
Dr Martin D. Provencher (academic supervisor)
Register here
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The BLOOM Study (Bridging Luteal Ovarian Hormones and Mood)
The Johns Hopkins Reproductive Mental Health Center, at the Johns Hopkins School of Medicine and the University of Virginia, are seeking individuals with regular menstrual cycles to participate in a research study on premenstrual syndrome (PMS) or premenstrual dysphoric disorder (PMDD), or mood changes in the week before a menstrual period. This study will also investigate the effects of antidepressants in managing PMS/PMDD.
We are looking for both women who DO experience premenstrual mood symptoms and women who do NOT experience premenstrual mood symptoms before their periods.
Participants will have one remote visit, which will include mood questionnaires, tracking their menstrual cycle, and providing blood samples. Following the remote visit, there will be 4-8 blood draws over a period of 1-2 months.
To be eligible for the study, participants must:
Be between the ages of 18 and 50
Have a regular menstrual cycle
Not taking hormonal birth control
Not using psychiatric medications
Participants can receive between $240 and $380 in compensation for completing the study.
Study Location: Johns Hopkins Reproductive Mental Health Center, Baltimore, MD
Contact Information:Research Assistant: Victoria Paone | vpaone1@jhu.edu
Principal Investigator: Liisa Hantsoo, Ph.D
Protocol# IRB00445770
Click here to complete the online screening. https://mrprcbcw.hosts.jhmi.edu/redcap/surveys/?s=DPM34KFP3XXMAPNR
Submit Your Research
Are you a researcher or student looking to recruit participants for your study on premenstrual disorders? We frequently receive inquiries from researchers seeking participants. We are eager to support and promote ethically approved studies that can advance understanding in this field.
If you would like your survey to be featured on this page, please complete the submission form below.
📌 IMPORTANT To be considered, you must provide proof of Ethics Board approval. To ensure meaningful and accurate data, please familiarize yourself with the strict diagnostic criteria for PMDD before proceeding.