Glutamate Imaging and Cognitive Testing for Depression
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial aims to understand the role of the brain's glutamate system in depression. Participants will undergo MRI (Magnetic Resonance Imaging) and PET (Positron Emission Tomography) scans to capture brain images, along with cognitive tests to evaluate thinking skills. The trial seeks individuals with depression or PTSD who are either medication-free or on specific medications, and who do not have other major health issues. Participants must have experienced a current depressive episode or PTSD symptoms, and participation may last 1-2 months. As an unphased trial, this study offers a unique opportunity to contribute to groundbreaking research that could lead to new insights into mental health conditions.
Do I need to stop my current medications to join the trial?
The trial requires participants to be medication-free for at least 2 weeks or to be on a permissible medication. The protocol does not specify which medications are permissible, so you may need to discuss your current medications with the study team.
Will I have to stop taking my current medications?
The trial requires participants to be medication-free for at least 2 weeks or to be taking a permissible medication. You may need to stop taking your current medications if they are not allowed in the study.
What prior data suggests that the MRI and PET scans are safe for participants?
Previous studies have shown that MRI (Magnetic Resonance Imaging) is safe for people. MRI uses strong magnets and radio waves to create detailed pictures of the body's organs and tissues, without using radiation, making it a low-risk imaging option.
PET (Positron Emission Tomography) scans use a small amount of radioactive material to assess how the body functions. Research on PET imaging indicates it is generally safe, though it involves exposure to low levels of radiation. The radiation amount is typically within safe limits and similar to other medical imaging tests.
Both MRI and PET are well-tolerated by most people. Some may experience mild discomfort, such as feeling enclosed during an MRI or a slight pinch from the injection for a PET scan. Overall, strong safety evidence supports the use of both methods in clinical settings.12345Why are researchers excited about this trial?
Researchers are excited about this trial because it uses advanced brain imaging techniques like MRI and PET scans to better understand depression. Unlike standard treatments that focus on altering neurotransmitter levels with medication, this approach aims to visualize brain chemistry and structure directly, offering a non-invasive way to observe changes in the brain's glutamate system. By combining these imaging techniques with cognitive assessments, researchers hope to uncover new insights into how depression affects brain function, potentially leading to more personalized and effective treatment options in the future.
What evidence suggests that this trial's treatments could be effective for depression?
Research has shown that MRI (Magnetic Resonance Imaging), a technique used in this trial, can help predict how well someone might respond to depression treatment. One study found that analyzing MRI data with machine learning accurately predicted treatment success 84% of the time and correctly identified 77% of those who would benefit. This suggests that MRI can effectively forecast who might benefit from depression treatments. Similarly, PET (Positron Emission Tomography) scans, another technique used in this trial, can predict treatment response by identifying specific brain activity patterns. Both imaging techniques are becoming valuable tools in personalizing and improving treatment plans for depression.23567
Who Is on the Research Team?
Irina Esterlis, PhD
Principal Investigator
Yale University
Are You a Good Fit for This Trial?
This trial is for adults aged 18-65 with certain psychiatric conditions like depression, bipolar disorder, or PTSD. It's also open to healthy individuals without any DSM-5 diagnosis. Participants must be English-speaking and medication-free or on approved meds for at least two weeks.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Imaging and Testing
Participants undergo MRI and PET scans, and participate in cognitive testing
Follow-up
Participants are monitored for safety and effectiveness after imaging and testing
What Are the Treatments Tested in This Trial?
Interventions
- Cognitive Testing
- MRI
- PET
Find a Clinic Near You
Who Is Running the Clinical Trial?
Yale University
Lead Sponsor
VA Office of Research and Development
Collaborator