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Identifying Neuro-cognitive-physiological Factors that Moderate Anxiety and Depression

Identifying Neuro-cognitive-physiological Factors that Moderate Anxiety and Depression

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00038002
Enrollment
300
Registered
2025-09-30
Start date
2025-09-11
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

F32.0, F32.1, F32.2, F32.8, F32.9, F33.0, F33.1 F33.2 , F33.8, F33.9, F34.1, F40.0, F40.1, F40.2, F40.8, F40.9, F41.0, F41.1, F41.2, F41.3, F41.8, F41.9

Interventions

Group 1: Individuals diagnosed with anxiety and/or depression disorders, undergoing task-based and resting-state fMRI, ECG, and blood pressure measurements, combined with cognitive tasks. Group 2: Hea

Sponsors

Max Planck Institute for Human Cognitive and Brain Sciences, Department of Neurology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: - Only for the anxiety and depression group: Psychiatric diagnosis of anxiety disorder (including panic attacks, agoraphobia, generalized anxiety, social anxiety, adjustment disorder with anxious reaction and anxiety-NOS) and/or mood disorder (major depression, dysphoria, adjustment disorder with depressive reaction, depressive episode). - Age 18-55 - Normal or corrected-to-normal vision - Voluntary participation and signing of the declaration of consent - German as a mother tongue or fluency in German (CEFR C1)

Exclusion criteria

Exclusion criteria: - Active psychosis - Diagnosis of bipolar disorder/ history of manic episodes - Significant suicidal intent requiring enhanced care - Presence of any contraindications for MRI examinations (see Appendix 1E MRI consent form) including claustrophobia, pacemakers, intracranial metal clips, cochlear implants, cerebrospinal fluid shunts, braces, and implanted medication pumps. - Neurological illnesses (e.g., epilepsy) or head trauma - Persons unable to give consent (e.g., in the case of dementia) - Pregnancy or planned pregnancy at the time of the study - Breastfeeding women - Lack of consent to the disclosure of incidental findings - Only for the control group: Diagnosis of anxiety and/or mood disorders - Only for the control group: Previous or current psychiatric diagnosis (not including ADHD)

Design outcomes

Primary

MeasureTime frame
Primary endpoints: 1.Examining whether the performance on the cognitive tasks and the associated brain responses and heart rate variations can accurately predict classification to health or diagnosis, using ML classifiers. 2.Examining whether the performance on the cognitive tasks and the associated brain responses and heart rate variations can accurately predict the level of symptom severity, using ML regressors. 3.Examining whether distinct cognitive performance, associated brain responses, heart rate variations can differentiate between subtypes across the anxiety and depression group and uniquely characterize each subgroup through advanced ML clustering analysis.

Secondary

MeasureTime frame
Analysis of the relationship between cognitive task performance, brain activity (fMRI), and physiological responses (HRV and BP) to better understand how these factors interact with symptoms.

Countries

Germany

Contacts

Public ContactThalia Richter

Max Planck Institute for Human Cognitive and Brain Sciences

richtert@cbs.mpg.de+4915566171180

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: May 1, 2026