EUDOR-A Multi-centre Research ProgramA Naturalistic, European Multi-centre Clinical Study of EDOR Test in adult patients with primary depressio
- Conditions
- Intentional Self-harmF32F33F31F34F38F39Depressive episodeRecurrent depressive disorderBipolar 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
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.
-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
Name Time Method
- Secondary Outcome Measures
Name Time Method