Your session is about to expire
← Back to Search
Neurostimulation
Models of Auditory Hallucination
N/A
Waitlist Available
Led By Philip R Corlett, PhD
Research Sponsored by Yale University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up approximately 13 months
Awards & highlights
No Placebo-Only Group
Summary
This trial uses TMS, a procedure that stimulates brain cells with magnetic fields, to help patients with psychosis who have persistent auditory hallucinations. The goal is to see if TMS can reduce these hallucinations by changing brain activity. TMS has shown potential in reducing auditory hallucinations in schizophrenia.
Eligible Conditions
- Schizophrenia
- Schizoaffective Disorder
- Auditory Hallucinations
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ approximately 13 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~approximately 13 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Conditioned Hallucinations Task Performance
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Active Control
Group I: TMS to cerebellumActive Control1 Intervention
This study will recruit a further 70 clinical voice hearers. Again, they will complete parallel forms of the conditioned hallucinations task on two occasions, separated by a week. They will receive excitatory TMS over the cerebellum (and sham on the other occasion, in a randomized counterbalanced order). Hypotheses: Exciting the cerebellum will increase belief-updating. If poor belief-updating contributes to conditioned hallucinations, increasing cerebellum engagement should decrease conditioned hallucinations and alter the belief-updating model parameter compared with sham TMS.
Group II: TMS to insulaActive Control1 Intervention
This study will recruit 30 clinical voice hearers (P+H+). They will complete two parallel forms of the conditioned hallucinations task (with different visual and auditory stimuli) on two occasions, separated by a week.
TMS and sham will be delivered in a randomized counterbalanced order. Hypothesis: Inhibiting the insula will decrease prior over-weighting. If this computational perturbation is responsible for conditioned hallucinations, then ameliorating it with TMS that increases insula engagement will decrease conditioned hallucination responses. Furthermore, the prior weighting parameter will be reduced following active TMS compared with sham.
Find a Location
Who is running the clinical trial?
National Institute of Mental Health (NIMH)NIH
2,936 Previous Clinical Trials
2,751,654 Total Patients Enrolled
256 Trials studying Schizophrenia
90,424 Patients Enrolled for Schizophrenia
Yale UniversityLead Sponsor
1,930 Previous Clinical Trials
3,033,473 Total Patients Enrolled
60 Trials studying Schizophrenia
4,338 Patients Enrolled for Schizophrenia
Philip R Corlett, PhDPrincipal InvestigatorYale School of Medicine
2 Previous Clinical Trials
239 Total Patients Enrolled
2 Trials studying Schizophrenia
239 Patients Enrolled for Schizophrenia