Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
1500 participants
OBSERVATIONAL
2015-06-09
2025-12-31
Brief Summary
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Detailed Description
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A major research finding in the field of Biological Psychiatry is that symptom-based categories of mental disorders map poorly onto dysfunctions in brain circuits or neurobiological pathways. Many of the identified (neuro)biological dysfunctions are "transdiagnostic", meaning that they do not reflect diagnostic boundaries but are shared by different ICD/DSM diagnoses. The compromised biological validity of the current classification system for mental disorders impedes rather than supports the development of treatments that not only target symptoms but also the underlying pathophysiological mechanisms. The Biological Classification of Mental Disorders (BeCOME) study aims to identify biology-based classes of mental disorders that improve the translation of novel biomedical findings into tailored clinical applications.
Methods:
BeCOME intends to include at least 1000 affected individuals (recruited through advertisements/self-referral or visits in the institute's outpatient clinic or in collaborating practices) with a broad spectrum of affective, anxiety and stress-related mental disorders as well as 500 individuals unaffected by mental disorders (advertisements/self-referral). After a screening visit, all participants undergo in-depth phenotyping procedures and omics assessments on two consecutive days. Several validated paradigms (e.g., fear conditioning, reward anticipation, imaging stress test) are applied to stimulate a response in a basic system of human functioning (e.g., acute threat response, reward processing, stress response) that plays a key role in the development of affective, anxiety and stress-related mental disorders. The response to this stimulation is then read out across multiple levels. Assessments comprise omics, physiological, neuroimaging, neurocognitive, psychophysiological and psychometric measurements. The multilevel information collected in BeCOME will be used to identify data-driven biologically-informed categories of mental disorders using cluster analytical techniques. Moreover, the subgroup of patients from the outpatient clinic of the Max Planck Institute of Psychiatry is followed-up at study days 14, 28 and 56 as well as 4 and 12 months after baseline for changes in a subset of parameters (omics, vital parameters and selected psychometric measures).
Discussion:
The novelty of BeCOME lies in the dynamic in-depth phenotyping and omics characterization of individuals with mental disorders from the depression and anxiety spectrum of varying severity. The investigators believe that such biology-based subclasses of mental disorders will serve as better treatment targets than purely symptom-based disease entities, and help in tailoring the right treatment to the individual patient suffering from a mental disorder. BeCOME has the potential to contribute to a novel taxonomy of mental disorders that integrates the underlying pathomechanisms into diagnoses.
Conditions
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Study Design
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OTHER
OTHER
Study Groups
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externally recruited participants
Self-referred affected and non-affected participants responding to advertisements
no intervention
no intervention
In-house patients
Patients seeking treatment in the outpatient clinic of the Max-Planck-institute of Psychiatry
no intervention
no intervention
Interventions
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no intervention
no intervention
Eligibility Criteria
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Inclusion Criteria
* or no mental disorder
Exclusion Criteria
* Current illness in the field of organic mental disorders;
* Affective disorders caused by a medical condition
* Organic mental disorders (e.g. dementia)
* Current disorders of schizophrenia;
* Current eating disorder;
* Mental retardation and profound developmental disorders;
* Severe neurological or internal medical illness;
* Posttraumatic or post-ischemic brain damage or elapsed cerebral hemorrhage;
* Acute suicidality;
* Pregnancy and postpartum period;
* Magnetic resonance imaging contraindications (e.g. non-MR compatible metal implants including cardiac pacemakers, claustrophobia);
* Myopia \<-6 D, which cannot be compensated by contact lenses or MR compatible glasses (Cambridge Research Systems, Rochester, UK);
* Current substance abuse;
* Current or past substance dependence;
* Risky alcohol consumption, screened with the Alcohol Use Disorder Identification Test - Consumption questions (AUDIT-C) and defined as score of ≥5 in males and of ≥4 in females.
18 Years
75 Years
ALL
Yes
Sponsors
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Max-Planck-Institute of Psychiatry
OTHER
Responsible Party
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Principal Investigators
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Elisabeth B Binder, Prof. Dr. Dr.
Role: PRINCIPAL_INVESTIGATOR
Max-Planck-Institute of Psychiatry
Locations
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Max Planck Institute of Psychiatry
Munich, Bavaria, Germany
Countries
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Central Contacts
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Facility Contacts
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References
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Sun R, Fietz J, Erhart M, Poehlchen D, Henco L, Bruckl TM; BeCOME study team; Czisch M, Saemann PG, Spoormaker VI. Free-viewing gaze patterns reveal a mood-congruency bias in MDD during an affective fMRI/eye-tracking task. Eur Arch Psychiatry Clin Neurosci. 2024 Apr;274(3):559-571. doi: 10.1007/s00406-023-01608-8. Epub 2023 Apr 23.
Bruckl TM, Spoormaker VI, Samann PG, Brem AK, Henco L, Czamara D, Elbau I, Grandi NC, Jollans L, Kuhnel A, Leuchs L, Pohlchen D, Schneider M, Tontsch A, Keck ME, Schilbach L, Czisch M, Lucae S, Erhardt A, Binder EB. The biological classification of mental disorders (BeCOME) study: a protocol for an observational deep-phenotyping study for the identification of biological subtypes. BMC Psychiatry. 2020 May 11;20(1):213. doi: 10.1186/s12888-020-02541-z.
Other Identifiers
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350-14
Identifier Type: -
Identifier Source: org_study_id
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