Neurofeedback to Treat Depression
Launched by UNIVERSITY OF PENNSYLVANIA · Dec 21, 2021
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial, titled "Neurofeedback to Treat Depression," is exploring a new treatment for people with Major Depressive Disorder (MDD). The study aims to help reduce negative thinking patterns that can make depression worse by using a method called real-time fMRI neurofeedback. This technique involves monitoring brain activity and providing feedback to participants, helping them focus on positive thoughts during therapy sessions. The trial is currently looking for participants aged 18 to 65 who meet specific criteria, such as having a confirmed diagnosis of MDD and a certain level of depression severity.
If you or someone you know is interested in participating, you would need to be able to read and understand English, provide consent, and have normal cognitive function. However, there are some restrictions; for example, pregnant women and those currently taking antidepressant medication or in therapy cannot join. Participants can expect to engage in sessions that include brain monitoring and feedback to help improve their mental health. This study is a promising step towards finding new ways to treat depression, and participants will be contributing to important research that could benefit many people in the future.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • gender, inclusive
- • adult aged 18 - 65 meets Diagnostic and Statistical Manual of Mental Disorders (DSM-5) criteria for MDD according to the Clinician-Administered MDD Scale for DSM-5 (unipolar depression or bipolar II depressed)
- • scores at least a minimum score of 16 on Montgomery Asberg Depression Rating Scale (MADRS)
- • normal cognition
- • participants must be able to read and understand English
- • participants must be able to provide consent
- Exclusion Criteria:
- • pregnancy (female participants)
- • outside age range
- • MRI contraindications (medical implant, claustrophobia, etc.)
- • use of psychoactive medication (including antidepressants) or currently in therapy
- • neurological disorder or any condition that in the view of the PI could impact brain data, cause depression, require medication that could cause depressive symptoms, or otherwise result in participant being unfit for study (for example, co-morbid psychotic, neurological disorders, developmentally or cognitively disabled/impaired, active alcohol or drug abuse/dependence within the past 6 months).
- • non-English speaking
- • non-correctable vision loss
- • refusal to provide informed consent
- • representing an active suicide risk
About University Of Pennsylvania
The University of Pennsylvania, a prestigious Ivy League institution located in Philadelphia, is renowned for its commitment to advancing medical research and improving healthcare outcomes. As a clinical trial sponsor, the university leverages its extensive resources, interdisciplinary expertise, and cutting-edge facilities to conduct innovative studies across various therapeutic areas. With a focus on translating scientific discoveries into clinical applications, the University of Pennsylvania fosters collaborations among leading researchers, clinicians, and industry partners, ensuring rigorous trial design and adherence to ethical standards. Through its dedication to excellence in research and education, the university plays a pivotal role in shaping the future of medicine.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Philadelphia, Pennsylvania, United States
Patients applied
Trial Officials
Yvette I Sheline, MD
Principal Investigator
University of Pennsylvania
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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