Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
30900 participants
OBSERVATIONAL
2021-10-12
2025-06-15
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
OTHER
Eligibility Criteria
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Inclusion Criteria
* at least one depressive episode preceding the current one;
* aged between 18 and 65;
* score of at least 8 on the Hamilton Depression Rating Scale (HDRS);
* signature of the information form and declaration of informed consent;
* elementary school certificate (as a minimum requirement for understanding the questions presented in the tests);
* native Italian speaker (or bilingualism).
Exclusion Criteria
* diagnosis of intellectual disability, epilepsy, neurodegenerative disorders;
* disorders related to the use of drugs or alcohol in the last 6 months (except nicotine and caffeine);
* pregnant or breastfeeding.
18 Years
65 Years
ALL
No
Sponsors
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Ministry of Health, Italy
OTHER_GOV
Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico
OTHER
Ospedale San Raffaele
OTHER
Responsible Party
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Benedetta Vai
Principal Investigator
Principal Investigators
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Benedetta Vai, PhD
Role: PRINCIPAL_INVESTIGATOR
IRCCS San Raffaele Scientific Insititute
Locations
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Benedetta Vai
Milan, , Italy
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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GR-2019-12370616
Identifier Type: -
Identifier Source: org_study_id
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