Improving Health Care in Major Depressive Disorder

NCT ID: NCT05816018

Last Updated: 2023-04-18

Study Results

Results pending

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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Recruitment Status

UNKNOWN

Total Enrollment

30900 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-10-12

Study Completion Date

2025-06-15

Brief Summary

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This project aims to improve the health care provided to people with major depressive disorder (MDD), a disease which is a top cause of disability worldwide. One of the main obstacles to a more effective health care in these patients is represented by clinical heterogeneity, which has not completely elucidated biological correlates. Using a large sample of people with MDD already recruited (n=29,400), the investigators develop a clustering algorithm based on genetic-environmental and brain imaging predictors aimed at identifying homogeneous MDD subgroups. The researchers will then link these subgroups with relevant health outcomes, such as disease recurrency and severity, well-being and functioning, risk of psychiatric and medical comorbidities (e.g. cardiovascular disorders). Replication in independent samples already recruited(n=1380) will prove the validity of the subgroups and expand their clinical characterization. The investigators will develop a classification tool to link the individual's characteristics to the relevant health outcomes and provide corresponding clinical recommendations. The prognostic support tool will be applied to newly recruited samples, feasibility and usefulness according to clinicians's opinion will be assessed (n=120, ongoing recruitment).

Detailed Description

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Conditions

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Major Depressive Disorder

Study Design

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Observational Model Type

COHORT

Study Time Perspective

OTHER

Eligibility Criteria

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Inclusion Criteria

* diagnosis of depressive episode in Major Depressive Disorder (DSM-5);
* 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 bipolar disorder, cyclothymic disorder, schizophrenia and other psychotic spectrum disorders, neurodevelopmental disorders;
* 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.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Ministry of Health, Italy

OTHER_GOV

Sponsor Role collaborator

Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico

OTHER

Sponsor Role collaborator

Ospedale San Raffaele

OTHER

Sponsor Role lead

Responsible Party

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Benedetta Vai

Principal Investigator

Responsibility Role 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

Site Status RECRUITING

Countries

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Italy

Central Contacts

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Benedetta Vai, PhD

Role: CONTACT

+393335652025

Irene Bollettini, PhD

Role: CONTACT

Facility Contacts

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Benedetta Vai, PhD

Role: primary

+393335652025

Other Identifiers

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GR-2019-12370616

Identifier Type: -

Identifier Source: org_study_id

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