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Repeated Real-time Biofeedback With 7-Tesla MRI for Treatment of Depression
RECRUITINGN/ASponsored by University of Oxford
Actively Recruiting
PhaseN/A
SponsorUniversity of Oxford
Started2026-06
Est. completion2031-06
Eligibility
Age18 Years – 65 Years
Healthy vol.Accepted
View on ClinicalTrials.gov →
NCT07694076
Summary
Previous work demonstrated that individuals are able to self-regulate their ventral tegmental area (VTA) activity using real-time biofeedback. The current study expands this approach to a larger sample with repeated training sessions to more robustly characterize the effects of VTA modulation. The study will assess change in mood and motivation-related measures, as well as neural activity and connectivity changes.
Eligibility
Age: 18 Years – 65 YearsHealthy volunteers accepted
Inclusion Criteria: * Male or female aged 18-65 years; * Meets DSM-5 criteria for major depressive disorder (MDD) as determined by the Structured Clinical Interview for DSM-5 Axis Disorders (SCID) or the Mini International Neuropsychiatric Interview (MINI); with a current major depressive episode. * Participants must have a level of understanding of the English language sufficient to agree to all tests and examinations required by the study and must be able to participate fully in the informed consent process. Exclusion Criteria: * Current or history of schizophrenia or other psychotic disorder, neurodevelopmental disorder, neurocognitive disorder or cognitive impairment * Active substance use disorder within the past 1 year; * Any unstable medical illnesses; * Women who are pregnant; * Any contraindications to MRI * Antidepressant medication initiated within 2 weeks of the Baseline Assessment and concomitant use of any other medication with central nervous system activity during active participation; * Active suicidal intent or plan.
Conditions2
DepressionMajor Depressive Disorder (MDD)
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Actively Recruiting
PhaseN/A
SponsorUniversity of Oxford
Started2026-06
Est. completion2031-06
Eligibility
Age18 Years – 65 Years
Healthy vol.Accepted
View on ClinicalTrials.gov →
NCT07694076