RecruitingPhase 4NCT06969755
Biomarkers to Enhance Early Schizophrenia Treatment
Sponsor
Northwell Health
Enrollment
180 participants
Start Date
Sep 30, 2025
Study Type
INTERVENTIONAL
Conditions
Summary
This study is recruiting participants who are experiencing a first episode of psychosis and who have certain genetic factors that may make them respond better to certain medications that are used to treat people with psychosis.
Eligibility
Min Age: 18 YearsMax Age: 35 Years
Inclusion Criteria8
- Aged 18 to 35.
- DSM5 diagnosis (as determined by the SCID5) of schizophrenia, schizoaffective disorder, schizophreniform disorder.
- Current positive symptoms rated ≥4 (moderate) on one or more of the following BPRS positive subscale items: unusual thought content, conceptual disorganization, hallucinatory behavior, suspiciousness.
- Preserved striatal connectivity, as determined by screening MRI scan
- Absence of the MC4R high-risk genotype, as determined by genetic testing
- Absence of the HLA-DQB1 high-risk genotype, as determined by genetic testing
- In an early phase of illness as defined by having taken antipsychotic drugs for a cumulative lifetime period of 4 weeks or less (with exceptions of very low doses for other off-label indications, e.g. sleep)
- Ability to provide informed consent
Exclusion Criteria12
- The patient reports or medical records state a serious neurological or endocrine disorder at screening that the investigator determines could interfere with the interpretation of the efficacy or safety measurements
- An abnormal EKG at screening that the investigator determines could interfere with the interpretation of the efficacy or safety measurements
- Any medical condition which requires treatment with a medication with psychotropic effects.
- Significant risk of suicidal or homicidal behavior (i.e. 'severe' risk on the Columbia Suicide Scale, a 'hostility' score of 7 on the BPRS, or an answer of 'yes' on questions 4,5 or 6 on the CDSS).
- Cognitive limitations, or any other factor that would preclude potential participants providing informed consent
- Contraindications to MRI (e.g. pacemaker).
- Meeting SCID-5 substance use disorder moderate or severe for any substance, other than nicotine within 3 months of screening visit. Meeting SCID5 substance use disorder mild for any substance other than cannabis, alcohol, or nicotine for less than 3 months prior to screening visit, or a positive urine baseline drug screen with a substance other than nicotine, alcohol, or cannabis
- Suspected DSM5 intellectual disability based upon clinical interview and psychosocial history, as well as screening with the Weschler Test for Adult Reading (IQ score <71)
- Prior psychosurgery
- Pregnancy (self-report)
- Seizure disorder (self-report)
- \-
Interested in this trial?
Get notified about updates and connect with the research team.
Interventions
DRUGaripiprazole
aripiprazole arm (titrated dose)
DRUGrisperidone
risperidone arm (titrated dose)
DRUGclozapine
clozapine (titrated dose)
Locations(2)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06969755
Related Trials
A Novel Blood Test as a Biomarker in Mental Health
NCT068561611 location
Effects of Smoking on Network Connectivity in Patients With Schizophrenia Symptoms in Scz Patients
NCT074419285 locations
Context-Aware Mobile Intervention for Social Recovery in Serious Mental Illness (R33)
NCT068659371 location
Effects of Schizophrenia and Bipolar Disorder on Exercise Capacity, Pulmonary Function, and Quality of Life
NCT073064681 location
Effectiveness of Digital Cognitive Behavioral Therapy for the Treatment of Depression: a Real-world Study
NCT068314351 location