Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Class |
|---|---|
| University of Cagliari | OTHER |
| Poznan University of Medical Sciences | OTHER |
Not provided
Not provided
Not provided
Not provided
Not provided
Major depressive disorder (MDD) is the most common psychiatric disease worldwide with a huge socio-economic impact. Pharmacotherapy represents the first-line treatment choice; however, only about one third of patients respond to the first trial and about 30% are classified as treatment-resistant depression (TRD). TRD is associated with specific clinical features and genetic/gene expression signatures. To date, single sets of markers have shown limited power in response prediction. The aim of this project is the development of a precision medicine algorithm that would help early detection of non-responder patients, who might be more prone to later develop TRD.
In this phase of the project a naturalistic cohort of 300 MDD patients will be recruited. The data collected will be used to assess, in real-world conditions, the capability of an innovative algorithm (integrating clinical, omics and gender data of other 300 patients con MDD) to predict the treatment outcomes. This project represents a proof-of-concept study. The obtained results will provide information about the feasibility and usefulness of the proposed approach, with the perspective of designing future clinical trials in which algorithms could be tested as a predictive tool to drive decision making by clinicians, enabling a better prevention and management of MDD resistance.
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Antidepressant | Drug | Antidepressant (AD) monotherapy or complex psychopharmacology such as two ADs or AD plus augmentation (second generation antipsychotics, mood stabilizers, lithium, FT3/FT4). Combination with diverse types of ongoing psychotherapy will be accepted, if commenced prior to baseline |
| Measure | Description | Time Frame |
|---|---|---|
| Clinical response | Symptom improvement as measured by the percent change in the Montgomery-Asberg Depression Rating Scale (MADRS) score | Baseline to 8 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Clinical response and remission | Symptom improvement as well as response and remission rates as according to the MADRS | Baseline to 2 weeks, to 4 weeks, to 8 weeks and 12 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Clinical response and remission self-reported | Changes in scores of depressive symptoms as measured by the Beck Depression Inventory II (BDI-II). Score on the BDI-II can range from 0 to 63 with higher scores indicating greater severity of depression. | Baseline to 2 weeks, to 4 weeks, to 8 weeks and 12 weeks |
| Clinical response and remission self-reported |
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
MDD in-patients or out-patients referred to psychiatric services are voluntarily enrolling in the study
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Bernhard T. Baune, Professor | Contact | 0049 251 8356664 | bernhard.baune@ukmuenster.de | |
| Alessandra Minelli, Dr | Contact | + 39 0303501255 | alessandra.minelli@unibs.it |
| Name | Affiliation | Role |
|---|---|---|
| Bernhard T. Baune, Professor | University Hospital Muenster | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Bernhard Baune | Recruiting | Münster | D-48159 | Germany |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| ID | Term |
|---|---|
| D003865 | Depressive Disorder, Major |
| ID | Term |
|---|---|
| D003866 | Depressive Disorder |
| D019964 | Mood Disorders |
| D001523 | Mental Disorders |
Not provided
Not provided
| ID | Term |
|---|---|
| D000928 | Antidepressive Agents |
| ID | Term |
|---|---|
| D011619 | Psychotropic Drugs |
| D002491 | Central Nervous System Agents |
| D045506 | Therapeutic Uses |
| D020228 | Pharmacologic Actions |
Not provided
Not provided
Not provided
Not provided
Not provided
Changes in scores of anxiety symptoms as measured by the Beck Anxiety Inventory (BAI). Score on the BAI can range from 0 to 63 with higher scores indicating higher level of anxiety. |
| Baseline to 2 weeks, to 4 weeks, to 8 weeks and 12 weeks |
| Psychosocial functioning | Changes in scores of psychosocial functioning as measured by the Functioning Assessment Short Test 24 items (FAST). All of items are rated using a 4-point scale. The global score is obtained when the scores of each item are added up. The higher the score, the more serious the difficulties are. | Baseline to 4 weeks, to 8 weeks and 12 weeks |
| Side effects | Changes in side effects assessed by the UKU Side Effect Rating Scale (UKU-SERS). All of items are rated using a 3-point scale. Score can range from 0 to 63 with higher scores indicating more side effects. | Baseline to 4 weeks, to 8 weeks and 12 weeks |
| Suicidal risk | Changes in scores of suicidal risk as measured by the Columbia-Suicide Severity Rating Scale (C-SSRS). Scores on the C-SSRS can range from 0 to 25 with higher scores indicating higher intensity of suicidal risk. Anyway any score greater than 0 is important and may indicate the need for mental health intervention. The suicidal behavior lethality rating is taken directly from the C-SSRS. | Baseline to 2 weeks, to 4 weeks, to 8 weeks and 12 weeks |
| Perceived stress | Changes in scores of perceived stress as measured by the Perceived Stress Scale-10 (PSS-10). Individual scores on the PSS-10 can range from 0 to 40 with higher scores indicating higher perceived stress. | Baseline to 4 weeks, to 8 weeks and 12 weeks |
| General Health and Quality of Life | Changes in scores of quality of life as measured by the Quality of Life Questionnaire (SF-36). Consisting of 8 domains. The scores for each domain range from 0 to 100, with higher scores indicating more favorable health status. | Baseline to 4 weeks, to 8 weeks and 12 weeks |
| D020164 | Chemical Actions and Uses |