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COMPLETED
NCT04450186
NA

Study Pilot - Hybrid EEG/fMRI Neurofeedback in Depressed Patients

Sponsor: Rennes University Hospital

View on ClinicalTrials.gov

Summary

Cognitive impairment is a common residual symptom after a depressive episode and expose patients to a risk of relapsing or therapeutic resistance. Neurofeedback (using ElectroEncephaloGraphy - EEG or functional Magnetic Resonance Imaging - fMRI) allows patients to self-regulate their cerebral activity, which is supposedly provided through an intelligible and motivating feedback. Recent results exhibited clinical improvement in depressed patients who underwent a fMRI neurofeedback protocol targeting the amygdala. Furthermore, prefrontal alpha activity was temporally correlated to variations of the BOLD signal in the amygdala. Simultaneous fMRI/EEG neurofeedback is hypothesized to potentialize its antidepressant effect. Our objective will be to test this assumption by conducting a double-blind randomized trial, and to prove the superiority of bimodal fMRI/EEG neurofeedback over fMRI neurofeedback alone in depressed patients. An original visual feedback will be provided and validated beforehand by a pilot study.

Key Details

Gender

All

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

31

Start Date

2020-08-10

Completion Date

2022-04-26

Last Updated

2026-06-12

Healthy Volunteers

Yes

Conditions

Interventions

OTHER

EEG/fMRI neurofeedback

EEG/fMRI neurofeedback

Locations (1)

CHU

Rennes, France