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:
- People aged 18 to 65 years old who have been diagnosed with a schizophrenia spectrum disorder (such as schizophrenia, schizoaffective disorder, or a related psychotic disorder) based on standard diagnostic criteria (DSM-5)
- People whose treating psychiatrist considers them to be in a clinically stable condition
- People whose antipsychotic medication has stayed the same for at least 4 weeks
- People who have not been admitted to an acute psychiatric ward in the 3 months before joining the study
- People who are able to give informed consent, as assessed by their treating psychiatrist, and who have signed a consent form
Who may not be able to join:
- People currently experiencing an active major depressive episode, as determined by their treating psychiatrist
- People currently experiencing active psychotic symptoms, such as delusions, hallucinations, or feelings of persecution above a certain severity level on a standard rating scale
- People with significant movement-related side effects from medication, above a certain threshold on a standard assessment scale
- People experiencing notable sedation from medication, such as drowsiness, slowed thinking, or slurred speech
- People who are actively using substances on a daily basis (such as cocaine), including certain medications used as substitution therapy (such as methadone)
- People with a history of unexplained fainting episodes that may have been seizures
- People with a history of multiple seizures or a diagnosis of epilepsy
- People with a progressive neurological condition such as multiple sclerosis or Parkinson's disease
- People with chronic uncontrolled medical conditions that could become dangerous if a seizure were to occur (such as certain heart conditions or severe asthma)
- People with metal objects or implants in their body, unless those implants have been confirmed to be safe for MRI scanning
- People with certain implanted medical devices in or near the head, including pacemakers, implanted medication pumps, vagal nerve stimulators, deep brain stimulators, TENS units, ventriculo-peritoneal shunts, or cochlear implants
- People with a reduced ability to feel heat or pain, or who have open wounds
- People with increased pressure inside the skull
- People with brain lesions caused by a genetic condition, stroke, tumour, cerebral palsy, severe head injury, or significant brain structural differences
- People with a history of a head injury that caused loss of consciousness for more than 15 minutes, or that led to lasting neurological effects
- People who are currently pregnant or breastfeeding; people who could become pregnant would need to be using active contraception to be considered for enrolment
- People with other significant ongoing medical conditions such as kidney failure, liver dysfunction, serious heart disease, cancer, or severe lung disease
- People who are unable to follow study procedures due to language barriers, psychological difficulties, intellectual disability, or dementia
- People who are under a legal obligation for psychiatric treatment
- People who have taken part in another clinical trial involving an investigational drug or medical device in the 30 days before this study, or who are currently in another trial
- People who have previously been enrolled in this same study
- The principal investigator running the trial, along with their family members, employees, or other people who depend on them
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.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Brief Negative Symptoms Scale - apathy subscale (BNSS-Apathy) at follow-up (FU) at T3. The primary endpoint will be assessed at baseline and all follow-up visits at week 1, 6 and 12.
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.