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EUDOR-A Multi-centre Research ProgramA Naturalistic, European Multi-centre Clinical Study of EDOR Test in adult patients with primary depressio

Conditions
Intentional Self-harm
F32
F33
F31
F34
F38
F39
Depressive episode
Recurrent depressive disorder
Bipolar affective disorder
Registration Number
DRKS00010082
Lead Sponsor
Emotra AB
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
1569
Inclusion Criteria

In- and outpatients with a primary diagnosis of depression according to the ICD-10, also in remission;
-Age: 18 years or older;
-Gender: Any;
-Signed Informed Consent.

Exclusion Criteria

-Patient’s dissent to participate in the study;
-In cases of diagnosed or suspected dementia, the patient should to be excluded unless there is a special interest by the centre. If included, this condition must be noted;
-In cases of known or suspected alcohol or other substance abuse, the patient has to be excluded unless there is a special interest by the centre. If included, this condition must be noted;
-Patient’s inability to understand the instructions for the EDOR Test;
-Serious problems of hearing.

Study & Design

Study Type
observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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