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 12 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 and re-evaluated at 2 months post-treatment. We expect significant clinical benefits from fMRI-based neurofeedback on drug-resistant hallucinations compared with the sham group.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Right-handed female/male between 18 to 60 y.o.
Schizophrenia (according to the DSM-5 classification)
Frequent auditory hallucinations (SAPS item #1 ≥ 4)
Stable medication for at least 30 days
Disqualifiers
Refusal to participate after clear and honest information about the study has been provided
Clinical condition incompatible with the study protocol (e.g. agitation, severe disorganization, catatonia)
Pregnancy
Contraindication to MRI scan: pacemaker, ferromagnetic vascular clip, ferromagnetic foreign body
Trial design
Parallel
Treatments tested in this trial
Active neurofeedback procedure
Other interventionPatients will perform 3 fMRI sessions. After one baseline fMRI run, two consecutive fMRI sessions (1/ day) during which they will continuously receive visual feedback (12 runs in total) computed from the fMRI signal analyzed with the hallucinations decoder. Patients will be trained to maintain the brain state associated with the no-hallucination state using appropriate coping strategies. Two post-treatment visits are scheduled at 1 and 2 months to assess hallucinations severity.
Sham neurofeedback procedure
Other interventionPatients will perform 3 fMRI sessions. After one baseline fMRI run, two consecutive fMRI sessions (1/ day) during which they will receive a random feedback (12 runs in total). Two post-treatment visits are scheduled at 1 and 2 months with the same clinical assessment than the active group.
Treatment groups
Trial outcomes
Primary outcomes
Change from baseline in the Auditory Hallucination Rating Scale (AHRS) measure of hallucinations severity
AHRS will be measured at t0 (randomization) and at 1 month after treatment Minimum score is 2, maximum score is 41, higher score indicates more severe symptoms.
Secondary outcomes
Change from baseline in Auditory Hallucinations Rating Scale (AHRS) measure
AHRS will be measured at t0 (randomization) and at 1 month after treatment The PANSS contains 7 positive symptom scales, 7 negative system scales, and 16 general psychopathology symptom scales. rate from 1 to 7 on each symptom scale. The total score is the sum of all scales with a minimum score of 30 and a maximum score of 210
Changes in global functioning relative to baseline
Global Assessment of Functioning (GAF) is a numeric scale be measured at t0 (randomization) and at 1 month after treatment Scores range from 100 (extremely high functioning) to 1 (severely impaired).
Changes in quality of life relative to baseline
SQLS score will be measured at t0 (randomization) and at 1 month after treatment
Changes in structural MRI markers relative to baseline
Cortical thickness will be measured at t0 (randomization) and at 1 month after treatment
Sponsors and contacts
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University Hospital, Lille
Lead sponsor
National Research Agency, France
Collaborator