Toward a Computationally-Informed, Personalized Treatment for Hallucinations
Launched by YALE UNIVERSITY · Apr 24, 2020
Trial Information
Current as of June 27, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is exploring new ways to treat auditory hallucinations, which are when people hear voices or sounds that aren’t there. These hallucinations can be very distressing, especially for those with conditions like schizophrenia. The researchers are using advanced computer models to better understand how the brain works in relation to these experiences. The goal is to develop personalized treatment options for individuals who currently do not respond well to traditional medications.
To be eligible for the study, participants need to be between 18 and 65 years old, speak English, and be right-handed. They should have a diagnosis of schizophrenia or related disorders and experience auditory hallucinations at least once a week. However, individuals with certain medical conditions, a history of substance use, or who are pregnant cannot participate. If you join the study, you can expect to work closely with the research team and undergo assessments that may help in understanding your condition better, potentially leading to new treatment options tailored just for you.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Age 18-65
- • English speaking
- • Right handedness
- • Diagnosed with schizophrenia schizoaffective, schizophreniform, schizotypal, or brief psychotic disorder
- • History of auditory verbal hallucinations occurring at least weekly
- Exclusion Criteria:
- • Current substance dependence or active use as determined by drug test.
- • Any neurological, medical or developmental problem that is known to impair cognition significantly
- • Contraindications for MR scanning including metallic implants of any kind, pacemakers and history of accidents with metal, claustrophobia
- • History of seizures
- • History of violence
- • History of suicide
- • Pregnancy (determined by urine pregnancy test)
- • Concurrent participation in any other intervention study
- • History of urinary retention
- • History of delirium
- • Current use of any cholinergic or anticholinergic medication
- • History of asthma, diabetes, and cardiovascular disease
- • Evidence of cardiovascular disease on EKG
- • Individuals who have been on dopamine-2 antagonists for less than 6 months (to limit risk of EPS)
About Yale University
Yale University, a prestigious Ivy League institution located in New Haven, Connecticut, is renowned for its commitment to advancing medical research and clinical innovation. With a rich history of academic excellence and a robust infrastructure for scientific inquiry, Yale serves as a leading sponsor for clinical trials aimed at improving patient care and developing new therapeutic approaches. The university's multidisciplinary teams of researchers and clinicians collaborate to conduct rigorous and ethical studies, leveraging cutting-edge technologies and methodologies to address critical health challenges. Through its dedication to fostering an environment of inquiry and discovery, Yale University plays a pivotal role in translating research findings into clinical practice, ultimately enhancing health outcomes for diverse populations.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
New Haven, Connecticut, United States
Patients applied
Trial Officials
Albert Powers, MD, PhD
Principal Investigator
Yale University
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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