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Depression Early Prediction Inventory

Depression Early Prediction Inventory - DEEP-IN

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00022486
Enrollment
600
Registered
2020-08-13
Start date
2020-10-01
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

F31 F32 F33 F34

Interventions

Group 1: In this study we will include 600 outpatient or (semi-)residential patients currently diagnosed with a depressive disorder according to ICD-10 criteria (unipolar depression F32, recurrent dep
WHO, 1992) yet being full or partial remitted and having a HDRS-Score (Hamilton-Depression-Rating-Score, Hamilton 1960) of max 20. In order to verify the retest-reliability and validity of the questio

Sponsors

Klinik und Poliklinik für Psychiatrie und Psychotherapie, LVR-Klinikum Düsseldorf, Heinrich-Heine Universität, Medizinische Fakultät, Düsseldorf
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. (semi-)residential and out patients 2. partial or fully remitted patients, HDRS =20 3. written consent after comprehensive information by the psychiatrist 4. patient being capable to understand the kind and needs of the study according to the investigators appraisal 5. Age between 18 and 65 6. currently being treated for a depressive disorder according to ICD-10 criteria as determined by the psychiatrist in the respective settings a) bipolar disorder F31, b) unipolar depression F32, c) recurrent depressive disorder F33, or d) persistent affective disorder F34

Exclusion criteria

Exclusion criteria: 1. insufficient knowledge of German language 2. acute suicidality 3. comorbidties, according to ICD-10 defined as F= organic, symptomatic mental disorder; F1 disorder due to psychotropic substances; F2 schizophrenia and delusional disorders; F84 pervasive developmental disorders (except F21 schizotypy) 4. Substance use/miss-use during the last 4 weeks 5. medical history of craniocerebral injury and/or loss of consciousness > 5 minutes 6. medical history of somatic/neurological disorders affecting the brain

Design outcomes

Primary

MeasureTime frame
The main objective of this project is the extraction of predictors and the development of a respective psychometric instrument in order to be able to calculate the risk for developing depression, with significance of bio-psycho-social risk factors and psychpathological aspects.

Secondary

MeasureTime frame
re-test-reliability and validity

Countries

Germany

Contacts

Public ContactZsuzsánna Balázsy

Tagesklinik und Ambulanzzentrum am LVR-Klinikum Düsseldorf Kliniken der Heinrich-Heine-Universität Düsseldorf

Zsuzsanna.Balazsy@lvr.de0211-922 3500

Outcome results

None listed

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