Schizophrenia Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You must have freely agreed to take part and signed a consent form
- You must be covered by a health insurance plan
- You must have been diagnosed with schizophrenia according to standard criteria (DSM-5), confirmed through a clinical interview
- Your schizophrenia must have been present for 20 years or less
- You must currently be receiving psychiatric care, either as a hospital inpatient, as an outpatient, or through a mandatory community psychiatric care programme
- Your overall health must be considered suitable for brain scanning, as judged by your doctor
- You must be able to understand, read, and write French
For one specific group within the trial:
- You must be experiencing hallucinations and have had them in the past 15 days, with a score of 4 or higher on a specific hallucination-related rating scale (confirm with trial site)
For the comparison group within the trial:
- You must not be experiencing any hallucinations and must have had none in the past 15 days, with a score of 1 on that same rating scale (confirm with trial site)
Who may not be able to join:
- People who are under a legal protection order or state guardianship
- People who cannot have an MRI scan — for example, due to severe claustrophobia or other medical reasons
- People who are deaf, whether from birth or due to illness or injury
- People considered to be at risk of suicide, as judged by their doctor
- People with moderate to severe learning disabilities, based on their medical records
- People with moderate to severe memory or thinking difficulties, based on their medical records
- People currently taking certain anticholinergic medications (such as Akineton, Artane, or Lepticur)
- People who have taken part in another clinical drug or medical device trial within the past 3 months
- People under any form of court-ordered legal protection
- Women who are pregnant, in labour, or breastfeeding
- People who are not able to give their own consent
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Martin Pastre, CHU de Nimes
Phone: 06 95 55 68 80
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Resting state of functional connectivity of the inferior colliculi region with other regions of the auditory network between groups; Default mode network patterns between groups
Can't join this trial?
Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.