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Personalized, Predictive, Precise & Preventive Medicine for Major Depression

P4D - Personalized, Predictive, Precise & Preventive Medicine for Major Depression

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06027177
Acronym
P4D
Enrollment
1000
Registered
2023-09-07
Start date
2023-09-30
Completion date
2025-08-31
Last updated
2023-09-07

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

Conditions

Major Depressive Disorder, Persistent Depressive Disorder

Brief summary

Depressive disorders are among the most common psychiatric disorders. However, this disorder is multifaceted, as are its etiological factors, and is not yet fully understood. Within the framework of the P4D study, 1000 patients with depression will be comprehensively examined. In addition to the recording of psychological factors by means of questionnaires and third-party assessments, imaging and electrophysiological procedures (functional and structural MRI, EEG) are used to assess brain structure and function. In addition, blood is drawn from the subjects to analyze these samples for various biological markers (e.g., genetics). Drug level measurements are also performed. The goal is to perform an in-depth characterization (phenotyping) of individuals with a depressive disorder. These findings could be used to individualize and improve therapy for depressive disorders.

Interventions

None listed

Sponsors

University Medicine Greifswald
CollaboratorOTHER
Wuerzburg University Hospital
CollaboratorOTHER
Goethe University
CollaboratorOTHER
University Hospital Schleswig-Holstein
CollaboratorOTHER
Hannover Medical School
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* MDD: ICD-10: F32.1-3, F33.1-3 first or recurrent depressive episode (confirmed by MINI-DIPS) and/or PDD: F34.1 * Symptom severity: Moderate to severe (MADRS ≥ 20). * First depressive episode before 50 years of age * Signed informed consent form * Capacity to consent

Exclusion criteria

* Acute Suicidality * Placement according to state law (e.g. §16/17 Nds. PsychKG) * The following diagnoses in the life course: Dementia, schizophrenia, schizoaffective disorder, bipolar disorder, substance dependence with currently necessary detoxification * Concurrent participation in other clinical trials that are not being conducted within the framework of the P4D project

Design outcomes

Primary

MeasureTime frameDescription
Remission after 7 weeks of treatmentBaseline and Follow-up (Week 7)The Montgomery-Asberg-Depression-Scale (MADRS) is used to measure the severity of depressive symptoms. A score lower 7 is the cut-off.

Secondary

MeasureTime frameDescription
Recording of psychometric changes in the clinical course of treatmentBaseline and Follow-up (Week 7)A range of psychometric information is collected. These include questionnaires, third party ratings and a cognitive assessment, as well as neuroimaging (functional and structural MRI), neurophysiology (EEG) and polysomnography (PSG).
Frequency of other concomitant treatments (e.g., additional psychotherapeutic treatment)Follow-up (Week 7)Psychotherapy sessions (individual and group therapy) are recorded for 7 weeks. Alternative treatments (e.g. transcranial magnetic stimulation and electroconvulsive therapy) are also recorded.
Treatment/study dropout ratesDrop-out rates are collected throughout the data collection period, over two years. Starting at study enrollment of the first subject until complete completion of the last subject.Dropout rates are recorded with reasons.
Attitudes (acceptance, fears, and prejudices) regarding biomarker-guided examinations and technical procedures among the populationThe survey will be conducted over a 2-week period in late August / early September 2023.Representative population survey
Patient-doctor relationshipBaseline and Follow-up (Week 7)The Patient-Doctor-Relationship-Questionnaire (PDRQ-9) is used to assess the quality of the therapeutic relationship.

Contacts

Primary ContactHelge Frieling, Prof. Dr.med
frieling.helge@mh-hannover.de+49 511 532-2427
Backup ContactHannah B Maier, Dr. med.
maier.hannah@mh-hannover.de+49 176 1532-8329

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 8, 2026