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Active, not recruiting Observational

Bipolar Disorder Integrative Staging: Incorporating Biomarkers Into Progression Across Stages

NCT07343739 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2023-11-08
Last updated
2026-01-15

Condition(s) studied

Bipolar Disorder

Investigational drug(s) / intervention(s)

psychometric clinical assessmentbiological acquisitionneuroimaging data

psychometric clinical assessment: Clinical assessment will further include the administration of psychometric scales and questionnaires focused on clinical status, childhood trauma experiences, cognitive profile and adherence pattern

biological acquisition: Biological samples for gene expression, inflammation, and microbiome analyses will be collected at baseline, T2 and T3.

neuroimaging data: MRI assessments will be performed using 3T scanners at T0, T2, and T3

Study summary

Bipolar disorder (BD) is a lifelong, recurrent condition with growing evidence supporting a neuroprogressive course, entailing the need to adopt staging models to guide stage-speci c interventions. Although different approaches have been proposed, their application remains limited and largely based on clinical features. BOARDING-PASS is an Italian government-funded, multicenter, prospective, and observational study aimed at advancing current knowledge of BD progression through the integration of clinical, biological, neuroimaging data, alongside machine learning (ML) methodologies. The study will enroll 120 subjects (age 18-70 years), classified according to the Kupka \& Hillegers' staging model, and recruited from three secondary-level psychiatric services in Italy. The primary outcome is the longitudinal assessment of clinical stage progression over an 18-month period, with evaluations conducted at baseline (T0), T1 (6 months), T2 (12 months), and T3 (18 months after baseline). At each time point, clinical variables will be collected, as well as clinical stages assigned. Additionally, at T0, T2, and T3, peripheral blood and unstimulated saliva samples will be collected to assess epigenetic regulation of gene expression - including DNA methylation, histone modi cations, and exosomal miRNAs - with a focus on key biomarkers such as C-reactive protein, proinflammatory cytokines, and BDNF, as well as microbial signatures of major oral bacterial phyla. Structural and resting state functional MRI scans will also be acquired at the same time points:structural data will be used to compute the structural connectome based on gyrification-based covariance networks, while resting-state data will be used to assess functional connectome alterations via graph theory metrics. Finally, all multimodal data will be integrated within a supervised ML algorithm based on Support Vector Machine, with the goal of developing a re ned, data-driven staging model for BD. BOARDING PASS project aligns with the growing need for a standardized, biologically informed staging framework that integrates clinical, inflammatory, epigenetic, and neuroimaging pro les to enhance prognostic accuracy and support tailored therapeutic interventions in BD.

Eligibility

Sex
ALL
Min age
18 Years
Max age
70 Years
Healthy volunteers
Accepted
Inclusion Criteria: 1. A range of bipolar spectrum manifestations meeting the criteria of the Kupka \& Hillegers' staging model 2. Both genders 3. Age ≥18 and ≤70 years 4. Written informed consent obtained Exclusion Criteria: 1. Inability to provide informed consent 2. Diagnosis of intellectual disability 3. Presence of a severe medical condition (e.g., previously diagnosed neurological disorders, including chronic migraine, hematological diseases, renal disorders, history of stroke, or diabetes mellitus, even if compensated; controlled hypertension allowed) 4. Current substance use disorder or within six months prior to screening

Primary outcome measure(s)

  • Clinical stage progression in Bipolar disorder — 18 months
    The primary outcome of the BOARDING PASS study is the longitudinal assessment of clinical stage progression in BD at 6, 12, and 18 months, according to the Kupka \& Hillegers' staging model.

Trial sites (1)

FacilityCityRegionStatus
ASST Fatebenefratelli Sacco Milan Italy
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07343739 on ClinicalTrials.gov ↗ ← All trials in Italy