Schizophrenia Spectrum and Other Psychotic DisordersBICEPSNCT06740383
Biomarkers/Biotypes, Course of Early Psychosis and Specialty Services
An observational study of Schizophrenia Spectrum and Other Psychotic Disorders and Schizophrenia, run by Beth Israel Deaconess Medical Center at 6 sites in United States.
Trial summary
The Biomarkers/Biotypes, Course of Early Psychosis and Specialty Services (BICEPS) study aims to understand the early stages of psychotic disorders like Schizophrenia, Schizoaffective Disorder, and Bipolar I Disorder. Read more about this study
- Who is it for?
- Ages 18 to 40 years
- Conditions the study is for
- Schizophrenia Spectrum and Other Psychotic Disorders, Schizophrenia, Delusional Disorder
- How many people
- 320 participants
- Where
- 6 sitesUnited States
- Study dates
- 1 Jan 2023to 30 Jun 2027
- Phase
- Observational
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 40 years
- All sexes
- No healthy volunteers
- Adult
Study population: Participants are recruited from 5 different sites across the United States including Boston, Dallas, Hartford, Chicago, and Georgia. The target population for this study includes individuals who meet DSM-5 criteria for a psychotic disorder (i.e., schizophrenia, schizophreniform, schizoaffective disorder, bipolar I disorder or major depression with psychotic features, delusional disorder, or psychosis N.O.S.). Participants will be between 18 and 40 years of age, males and females, of all races and ethnicities who are experiencing early course psychosis.
Who may be able to join
- Males and females, all races and ethnicities
- 18-40 y/o
- Meet DSM-5 criteria for a psychotic disorder, i.e. schizophrenia, schizophreniform, schizoaffective disorder, or bipolar I disorder or major depression with psychotic features, delusional disorder or psychosis N.O.S.
- Able to read, speak, and understand English
- Able and willing to provide written informed consent, and willing to commit to the study protocol
- Illness duration from psychosis onset less than or equal to 4 years
- At baseline only: receiving both psychopharmacology and psychotherapy
Who cannot join
- Estimated premorbid intellectual ability <70 (WRAT-4, Word Reading subtest, age-corrected standardized score)
- Neurological or medical disorder that may affect brain function (seizure disorder, traumatic brain injury with a loss of consciousness greater than or equal to 30 min, history of stroke, AIDS, etc.)
- Psychoses secondary to substance use i.e., Comorbid DSM-5 diagnosis of alcohol or substance use disorders that may explain the diagnosis of psychotic disorders (individuals with cannabis use disorders unrelated to psychosis onset will be allowed. Participants encouraged to abstain from substances for 24 hours prior to lab visits)
- MRI-Specific Exclusion Criteria:
- Pregnant women
- Presence of ferromagnetic objects in body
- Weight or body size exceeding scanner capacity (>300 lbs)
- Claustrophobia
Trial locations and contacts
6 sites in 1 country. Contact the study team or a site near you to ask about taking part.
Brendan Stiltner, BA contact
6 sites in 1 country
United States6 sites, 6 recruiting
- Recruiting
University of Georgia
Athens, Georgia, 30602
Brett Clementz, PhD, 706-542-2174, clementz@uga.edu
Brett Clementz, PhD
- Recruiting
McLean Hospital
Belmont, Massachusetts, 02478
Kathryn E. Lewandowski, PhD, 617-855-2886, klewanowski@mclean.harvard.edu
Kathryn E Lewandowski, PhD
- Recruiting
Beth Israel Deaconess Medical Center
Boston, Massachusetts, 02215-5400
Matcheri S. Keshavan, MD, 617-754-1256, mkeshava@bidmc.harvard.edu
- Recruiting
University of Chicago Medical Center
Chicago, Illinois, 60637
Sarah K. Keedy, PhD, 773-834-7178, skeedy@bsd.uchicago.edu
Elliot S. Gershon, MD, egershon@bsd.uchicago.edu
- Recruiting
University of Texas Southwestern Medical Center
Dallas, Texas, 75390
Carol Tamminga, MD, 214-404-2284, carol.tamminga@UTSouthwestern.edu
Carol Tamminga, MD
- Recruiting
Hartford Hospital
Hartford, Connecticut, 06102
Godfrey Pearlson, MA, MBBS, 860.545.7757, Godfrey.Pearlson@HHChealth.org
Godfrey Pearlson, MA, MBBS
About this study
The Biomarkers/Biotypes, Course of Early Psychosis and Specialty Services (BICEPS) study aims to understand the early stages of psychotic disorders like Schizophrenia, Schizoaffective Disorder, and Bipolar I Disorder. It involves gathering mental health information, brain scans (MRI), eye movement patterns (Eye-Tracking), and brain electrical waves (EEG) data from individuals who have experienced these disorders in recent years. Participants will be involved for about a year, with four visits over this period. Screening procedures, lasting approximately 3 hours, include tests for drug use, a pregnancy test for eligible women, clinical interviews about feelings and experiences, psychiatric and family history interviews, and a medical history review. Research procedures for eligible participants include DNA collection, a neuropsychological test battery, EEG, eye-tracking, and MRI. These procedures will help researchers understand brain function, genetics, and cognitive abilities related to psychotic disorders. Follow-up visits at 1-month, 6-month, and 12-month intervals involve modified clinical interviews and repeating neuropsychological tests to track changes over time. Participants may opt to provide DNA samples for genetic analysis, undergo various cognitive tests, EEG to record brain waves, eye-tracking to monitor eye movements, and MRI scans to visualize brain structure. Follow-up visits at regular intervals will help researchers track changes in symptoms and cognitive function. This study provides comprehensive insight into the onset and progression of psychotic disorders and offers valuable information for patients, families, and healthcare providers involved in managing these conditions. Our goal is to better understand whether a combination of biological markers and different types of people (BT1, BT2, BT3) can help us predict how well individuals with early psychosis respond to specialized care. We expect that those in BT3 will have the best outcomes, BT2 will have intermediate outcomes, and BT1 will have the poorest outcomes. Even though BT1 and BT2 might start with similar cognitive issues, their biology might lead to different responses to treatment. This research can help us understand which treatments work best for different people with early psychosis.
Read the detailed description
This proposal seeks to characterize the early course of psychotic disorders and to identify clinical and biological predictors of outcome. The large sample (=320) required will necessitate a multi-site study. All B-SNIP sites have coordinated specialty services for early course psychosis and have harmonized study procedures for uniform data collection. Each site will recruit 1/5 of the participants; The project will be managed by an all-site steering committee meeting weekly. Boston will be the coordinating site.
The outcome of early course psychosis (EP) is heterogeneous, ranging from early full recovery to treatment resistance and functional decline from the onset of illness. The ability to predict individual level outcomes would be highly valuable for treatment planning and for tailoring the duration and intensity of psychosocial and pharmacological interventions. Clinical features related to early psychosis onset are poor predictors of remission and recovery. At the same time, the field has not yet established the clinical utility of promising findings from decades of biomarker development/neuroscience research, especially in EP patients for whom empirically guided treatment planning may have the greatest impact. For example, neurocognitive, electroencephalographic (EEG) and imaging biomarkers early in the illness may predict outcome, but used individually, their prognostic value is limited. Multivariate approaches to clinical and neurobiological features may offer better value for outcome prediction.
Toward this goal, we will leverage the biomarker (EEG, eye movement testing, and neurocognition) based categorization of a cross-diagnostic sample of psychosis (biotypes) developed, replicated and validated by our Bipolar-Schizophrenia Network for Intermediate Phenotypes (B-SNIP) consortium. We have shown that Biotype-1, characterized by impaired cognition and decreased sensorimotor responses to salient stimuli is associated with the most severe impairments in functioning. Biotype-2 have the same level of cognitive impairment as Biotype-1 but increased sensorimotor reactivity. Biotype-3 cases are relatively normal on these measures and have the least impairments. These subgroups are not synonymous with DSM diagnosis and are not captured by any individual variable. We do not know if this categorization is predictive of symptomatic and functional outcome, given the cross-sectional design of B-SNIP. We will use the B-SNIP battery with EP participants in the context of Coordinated Specialty Care (CSC) treatment programs for EP available at established B-SNIP sites. Our overall goal is to identify biomarkers/Biotypes that predict clinical and functional outcome to CSC in EP. This success could guide targeted interventions in CSC programs. For those unlikely to have a successful CSC outcome, other targeted interventions could be developed and implemented. We have active EP Clinics in the consortium; each will enter about16 patients/year, 80/year overall, providing 320 EP (schizophrenia, schizoaffective disorder, psychotic bipolar disorder and schizophreniform disorder participants with approximately 240 completer cases, assuming 25% attrition) enrolled during the first 4 years of the proposed funding period. All EP cases will be tested with B-SNIP biomarker assessments at baseline, and the clinical and cognition assessments will be repeated at 1, 6, and 12 months. We will use an adapted version of the B-SNIP biomarker battery (called ADEPT) which can be implemented in under-resourced, community settings.
SIGNIFICANCE AND BACKGROUND FOR THE STUDY Schizophrenia and related psychoses cause enormous suffering for affected individual and their families and caregivers. They have a lifetime prevalence of around 3%, and cost ~ $155 billion per year in direct healthcare and indirect societal costs in the USA [5]. Relapse and poor response to treatment contribute to a significant illness burden due to high rates of hospitalization and poor social and occupational functioning. About 20% of early course psychosis (EP) cases relapse in year 1, and about 40% by year 2 [6]. Mortality is increased four-fold in EP compared to the general population [7]. EP outcomes are highly variable [8] with multiple trajectories, i.e. episodic vs persistent, initial remission vs treatment resistance [9-11]. Given this heterogeneity, actionable outcome predictors are needed to reliably individualize care for EP [12].
- Conditions
- Schizophrenia Spectrum and Other Psychotic Disorders, Schizophrenia, Delusional Disorder, Bipolar 1 Disorder, Schizoaffective Disorder, Psychosis Not Otherwise Specified
- Keywords
- schizophrenia, bipolar disorder, schizoaffective disorder, schizophreniform, major depression, psychosis, delusional disorder, Biotypes, Biomarkers, coordinated specialty care
- Medical subject headings
- Schizophrenia Spectrum and Other Psychotic Disorders, Schizophrenia, Schizophrenia, Paranoid, Psychotic Disorders, Bipolar Disorder, Depressive Disorder, Major
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Individuals with Early Psychosis enrolled in Coordinated Specialty Care Clinics | In this naturalistic longitudinal study, we administer the B-SNIP biomarker batter to individuals with Early Psychosis (EP) in EP clinics with Coordinated Specialty Care treatment programs to characterize outcome trajectories and biotypes. EP individuals of both sexes, age 18-40 will be included after they meet study criteria and provide informed consent. Individuals with psychosis duration < 4 years will be included. Individuals in this cohort of EP are diagnosed with Schizophrenia, Schizoaffective Disorder, Schizophreniform, Bipolar I Disorder with psychotic features, Delusional Disorder, Major Depressive Disorder with psychotic features, and Psychosis Not Otherwise Specified. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Treatment Response
>30% reduction in Positive and Negative Syndrome Scale (PANSS) score
Measured: From enrollment at baseline to end of study at 1 year
Symptomatic Remission
Score of ≤ 3 on 8 core on the Positive and Negative Syndrome Scale (PANSS) items (P1, P2, P3, 1, N4, N6, N7, G5, and G9) for at least one month
Measured: From enrollment at baseline to end of study at 1 year
Functional Remission
Score ≥ 7 on Global Functioning Role and Social Scales
Measured: From enrollment at baseline to end of study at 1 year
Relapse
- Positive and Negative Syndrome Scale (PANSS) score of ≥ 4 for a psychosis item (P1, P2, P3, and P6) and ≥ 25% increase on the total PANSS score or ≥ 10 points and 2) an increased level of care, i.e. hospitalization, ER visits, etc.
Measured: From enrollment at baseline to end of study at 1 year
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 Dec 2024
- Study start1 Jan 2023
- Primary completion30 Jun 2027 (estimated)
- Study completion30 Jun 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Schizophrenia Spectrum and Other Psychotic DisordersStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 320 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Beth Israel Deaconess Medical Center
- Sponsor type
- University, hospital or other
- Collaborators
- University of Chicago, University of Texas Southwestern Medical Center, Yale University, Hartford Hospital, University of Georgia, Mclean Hospital, National Institute of Mental Health (NIMH)
- Responsible party
- Principal investigator, Matcheri S. Keshavan MD, Beth Israel Deaconess Medical Center
- Investigators
- Matcheri S. Keshavan, MD, Principal investigator, Beth Israel Deaconess Medical Center
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06740383
- Sponsor's protocol ID
- 2022P000622
- Other IDs
- R01MH127174-03
- Acronym
- BICEPS
- Status last verified
- Mar 2026
- First submitted
- 13 Dec 2024
- Last updated
- 10 Mar 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: The study team includes a dedicated staff member, Noora Al-Musawe, who is responsible for data preparation and sharing. Since the beginning of the study and during the reporting period, we have been adherent with the data sharing plan and guidelines. The study has been registered in NIH/NIMH Data Archive (NDA) (Study#: C4330). Data Submission Agreement is in place. The data will be uploaded to NDA during regular data sharing cycles.