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fMRI-based Neurofeedback to Relieve Drug-resistant Auditory Hallucinations

Study acronym: INTRUDE
StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 2 years 3 months later Jul 2026 → Nov 2028
See other at-risk trials from University Hospital, Lille

Record History

See every version on ClinicalTrials.gov ↗

  1. Notable Primary and study completion pushed from Jul 2026 to Nov 2028
    • Eligibility criteria expanded, about 77 words
    • Secondary endpoints: 9 to 6
  2. Notable Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 0 to 1
    • Start date changed from estimate of Dec 2022 to Aug 26, 2022
    v3
  3. Notable Primary and study completion dates: Feb 2025 to Jul 2026
    • Start date: Apr 2021 to Dec 2022
    v2
  4. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT04798131
Lead Sponsor University Hospital, Lille
Collaborators: National Research Agency, France
Conditions
(from sponsor)
Schizophrenia, Hallucinations, Auditory, Hallucinations, Visual
Related terms Hallucinations, Schizophrenia
Enrollment 84 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov