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Improving Health Care in Major Depressive Disorder

Improving Health Care in Major Depressive Disorder: a New Prognostic Tool Based on Gene Environment and Neuroimaging Signatures

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05816018
Acronym
DepType
Enrollment
30900
Registered
2023-04-18
Start date
2021-10-12
Completion date
2025-06-15
Last updated
2023-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Major Depressive Disorder

Brief summary

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).

Interventions

None listed

Sponsors

Ministry of Health, Italy
CollaboratorOTHER_GOV
Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico
CollaboratorOTHER
Ospedale San Raffaele
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
The depressive statusAssessment at the time of recruitmentAssessment of the severity of disease using the Self-report Inventory Of Depressive Symptoms (IDS-SR) (Rush et al., 1996) with minimum-maximum values 0-116, higher scores mean a worse outcome, regarding the last week.
The self-report depressive symptomatologyAssessment at the time of recruitmentAssessment of the depressive characteristics, using the Beck Depression Inventory (BDI) (Beck et al., 1961) with minimum-maximum values 0-39, higher scores mean a worse outcome, regarding the last 2 weeks.
The clinical evaluation of depressive symptomatologyAssessment at the time of recruitmentAssessment of the presence of depressive status, Hamilton Depression Rating Scale (HDRS) (Hamilton, 1967) with minimum-maximum values 0-69, higher scores mean a worse outcome, regarding the current state.
The rate of cardiovascular and/or cardiometabolic diseasesAssessment at the time of recruitmentAssessment of the presence/absence of lifetime and current cardiometabolic and/or cardiovascular diseases (e.g. diabetes, arterial hypertension, pulmonary arterial hypertension) based on extracted data from medical records and chart.

Secondary

MeasureTime frameDescription
The quality of functioning and well-beingAssessment at the time of recruitmentAssessment of current and lifetime quality of life and well-being using the WHO Quality of Life-BREF (WHOQOL-BREF) (World Health Organization, 1996): the minimum and maximum values are 0-118, higher scores mean a better outcome, regarding the last 2 weeks.

Countries

Italy

Contacts

Primary ContactBenedetta Vai, PhD
vai.benedetta@hsr.it+393335652025
Backup ContactIrene Bollettini, PhD
bollettini.irene@hsr.it

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026