About this trial
The INTRUDE trial aims at assessing the efficacy of an fMRI-based neurofeedback procedure on drug-resistant auditory hallucinations. Hallucinations are complex and transient mental states associated with subtle and brain-wide patterns of activity for which we were recently able to validate an fMRI multivariate decoder. Based on this progress, we can track patients' hallucinatory status using real-time fMRI. We will test whether schizophrenia patients with drug-resistant hallucinations can be trained to maintain the brain state associated with a no-hallucination condition using appropriate strategies and thus reduce overall severity. We will refer to a double-blind randomized placebo-controlled design. A total of 86 patients will be enrolled and equally split in an active neurofeedback group (n=43) and a sham group (n=43), matched for sex, age and PANSS scores. Each patient will benefit from 4 runs of either active or sham neurofeedback. The primary outcome measure will be the mean decrease of AHRS scores relative to baseline, and at 1 month post-treatment. We expect significant clinical benefits from fMRI-based neurofeedback on drug-resistant hallucinations compared with the sham group.
Eligibility criteria
Qualifiers
Schizophrenia (according to the DSM-5 classification)
Frequent auditory hallucinations (SAPS item #1 ≥ 4)
Stable medication for at least 30 days
Absence of chronic neurological disorder (including seizure)
Disqualifiers
Pregnancy
Contraindication to MRI scan
Claustrophobia
No social insurance
Trial design
Treatments tested in this trial
- Active neurofeedback procedure
- Sham neurofeedback procedure
Treatment groups
Sponsors and collaborators
University Hospital, Lille
Lead sponsor
National Research Agency, France
Collaborator