Individuals with the Fragile X premutation are at an increased risk for depression, other psychiatric conditions, and developing Fragile X tremor/ataxia syndrome (FXTAS). Our goal is to better understand the different mechanisms within the brain that contribute to the development of psychiatric conditions, including depression. Doing so will allow us to establish better prevention and intervention efforts within this population.
Q: Who can take part in this study?
We are currently recruiting females between 18-60 who carry the FMR1 premutation.
Q: What will participation involve?
Participation involves four types of data collection:
- Web-based questionnaires.
- In-person assessments that involve responding quickly to shapes and viewing emotional stimuli.
- Gathering a variety of biological measurements such as brain activity (EEG and/or MRI), heart rate activity, and a blood draw.
- Interviews about your feelings and experiences.
Q: How will this project help the Fragile X community?
We hope that our data will impact the broader community of individuals with the Fragile X premutation and depression by improving our understanding of brain mechanisms and treatment needs.
Q: Will I need to travel?
All assessments and tests for this study are done in person and at Purdue in West Lafayette, Indiana. Travel reimbursement may be available for folks who are commuting more than 45 minutes from the Purdue campus.
Q: How can I get more information?
This project is led by Dr. Dan Foti and Dr. Bridgette Tonnsen in the Department of Psychological Sciences at Purdue University. To learn more, please complete the form below and they will contact you.
This study is funded by Purdue University and the Indiana Clinical & Translational Sciences Institute. Photo courtesy of Matthew Thomas of Purdue University.
View More Opportunities
The UC Davis MIND Institute is currently recruiting study research participants. The study’s goal is to better understand the ways in which characteristics of mothers and fathers and relationships within the family influence the language learning environment of young boys with Fragile X syndrome.
This survey will help support families in the Early Check study in NC whose newborns have been diagnosed with Fragile X and inform the design of an early intervention program for these babies.
RTI Int’l and UNC at Chapel Hill are conducting a research study to learn more about early development of young children with Fragile X in North Carolina, and the experiences of their parents when obtaining the diagnosis and early intervention services.
A survey to measure levels of behavior. When someone with FXS is experiencing anxiety, describe what you see and hear, and how the experience impacts your/their quality of life.