Trials / Unknown
UnknownNCT04450186
Study Pilot - Hybrid EEG/fMRI Neurofeedback in Depressed Patients
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 30 (estimated)
- Sponsor
- Rennes University Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | EEG/fMRI neurofeedback | EEG/fMRI neurofeedback |
Timeline
- Start date
- 2020-08-10
- Primary completion
- 2021-08-01
- Completion
- 2021-12-01
- First posted
- 2020-06-29
- Last updated
- 2020-10-22
Locations
1 site across 1 country: France
Source: ClinicalTrials.gov record NCT04450186. Inclusion in this directory is not an endorsement.