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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.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record

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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
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.

Matcheri S. Keshavan, MD contact

617-754-1256

mkeshava@bidmc.harvard.edu

Brendan Stiltner, BA contact

bstiltne@bidmc.harvard.edu

6 sites in 1 country

United States6 sites, 6 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

    Recruiting

Other trials in United States

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].

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 groups in NCT06740383
Study groupRoleWhat they receive
Individuals with Early Psychosis enrolled in Coordinated Specialty Care ClinicsIn 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.

  1. Treatment Response

    >30% reduction in Positive and Negative Syndrome Scale (PANSS) score

    Measured: From enrollment at baseline to end of study at 1 year

  2. 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

  3. Functional Remission

    Score ≥ 7 on Global Functioning Role and Social Scales

    Measured: From enrollment at baseline to end of study at 1 year

  4. Relapse

    1. 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.

  1. First posted18 Dec 2024
  2. Study start1 Jan 2023
  3. Primary completion30 Jun 2027 (estimated)
  4. Study completion30 Jun 2027 (estimated)

Resources

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)
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.

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