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Neural and behavioral markers for the motivational negative symptoms of schizophrenia – a longitudinal approach

Neural and behavioral markers for the motivational negative symptoms of schizophrenia – a longitudinal approach - SyMoNe

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00011405
Enrollment
192
Registered
2017-04-05
Start date
2019-05-17
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

F20 F25

Interventions

Group 1: Patients with schizophrenia will be examined with respect to negative symptoms using psychopathological interviews, behavioral tasks and functional magnetic resonance imaging Group 2: Healthy

Sponsors

Charité - Universitätsmedizin BerlinKlinik für Psychiatrie und Psychotherapie
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: In order to be eligible to participate in this study, all participants must meet all of the following criteria: • 18-60 years old • Written informed consent In patients the diagnostic criteria are: • DSM-5 diagnosis of schizophrenia on the basis of the Structured Clinical Interview for DSM-5 (SCID-I) • Clinical stability as judged by the treating psychiatrist and indicated by no change in medication in the two weeks prior to the initial assessment

Exclusion criteria

Exclusion criteria: Any potential subject who meets any of the following criteria will be excluded from participation in this study: • Any previous neurosurgery or neurological disorder, including epilepsy • History of head injury resulting in unconsciousness lasting at least 1 hour • Pregnancy or lactation • Any contraindications for MRI such as ferromagnetic/non-MRI-compatible items or medical devices on or in the body (for example pacemaker, brain stimulator, clips, metal implants) • sensorineural hearing loss of 30dB or more or history of tinnitus • Incompetency to fully comprehend the purpose of the study or to make a rational decision whether or not to participate In patients additional exclusion criteria are: • Benzodiazepine use of more than 1mg lorazepam equivalents per day • Comorbid axis-I disorder

Design outcomes

Primary

MeasureTime frame
Strength of association between neural and behavorial markers with motivational negative symptoms

Secondary

MeasureTime frame
(1) The association between the neurobehavioral marker and apathy is reproducible across centers. (2) The association between the neurobehavioral marker and apathy is stable over the time of 3 months. (3) The neurobehavioral marker at the initial assessment will predict the level of negative symptoms 9 months later.

Countries

Germany, Switzerland

Contacts

Public ContactFlorian Schlagenhauf

Charité-Universitätsmedizin Berlin

florian.schlagenhauf@charite.de+49 30 450 517369

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026