In recent years, measurement-based care (MBC) has been gaining more attention in the treatment of depression because it allows psychiatrists to individualize treatment decisions for each patient based on the change of psychopathology and tolerance toward antidepressants. Several studies, such as the Sequenced Treatment Alternatives to Relieve Depression (STAR\*D) trial using MBC, found that MBC-informed sequential algorithms can be successfully integrated into clinical practice and improve patients' outcomes However, despite a strong theoretical rationale for MBC and data supporting the ability to implement MBC in clinical practice settings, there is currently no randomized controlled trial in MDD patients comparing MBC with usual/standard care. The investigators compare MBC with clinician's treatment decisions, standardizing care to two commonly prescribed antidepressants. Therefore, the aim of this study is to determine the effects of MBC in patients with MDD compared to standard treatment (ST). The research hypothesis is that compared to ST, the estimated time to response and to remission would be significantly shorter in the MBC group without increased dropout rates and side effect burden.
Objective: To compare the effectiveness and feasibility of the measurement-based care (MBC) in the treatment of depression with clinician's treatment decisions, standardizing treatment (ST, clinicians' choice decisions) to two commonly prescribed antidepressants. Methods: Selecting the patients in psychiatric hospitals and general hospitals with depression, with multi-center randomized controlled study design. Refer to STAR-D "measurement-based care" mode, to establish the whole measurement-based evaluation system. Eligible patients will be randomly assigned to 24 weeks of MBC or ST, restricting treatment to paroxetine (20-60mg/day) or mirtazapine (15-45mg/day) in both groups. the ST group will maximize simulate of the actual clinical situation, and the patients of the MBC group are required to complete the prospective Life-chart Methodology (LCM-p), 16-item Quick Inventory of Depressive Symptomatology Self-Report (QIDS-SR16) and other related symptoms and side effects of self-assessment, the doctor will make a comprehensive assessment according to the results of self-assessment, adjust treatment according to research programs. This is 1-year follow-up study; the independent members will have a blinded assessment in the baseline visit and each point of view. Depressive symptoms are measured using the Hamilton Rating Scale for Depression (HAMD) and QIDS-SR.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
164
Patients in both groups (MBC or ST) receive open-label paroxetine (20-60mg/day) within the therapeutic dose range recommended by the Guidelines for the Prevention and Treatment of Major Depression in China.
Patients in both groups (MBC or ST) receive open-label mirtazapine (15-45mg/day) within the therapeutic dose range recommended by the Guidelines for the Prevention and Treatment of Major Depression in China
Beijing Anding Hospital
Beijing, Beijing Municipality, China
The estimated time from randomization to response and remission according to Hamilton Rating Scale for Depression (HAMD) total score.
Response was defined as ≥50% decrease in the baseline HAMD total score; remission was defined as the HAMD total score ≤7
Time frame: From randomization to response and remission (24 week))
The changes of Hamilton Rating Scale for Depression (HAMD) total score
To measure the change of the severity of depressive symptoms
Time frame: From randomization to endpoint (Week 24)
The incidence and nature of overall adverse events
Time frame: From enrollment to endpoint (Week 24)
The incidence and nature of drug-related adverse events
Time frame: From enrollment to endpoint (Week 24)
The number of subject withdrawal due to adverse events during double-blind phase
Time frame: From randomization to endpoint(Week 24)
The changes of Quick Inventory of Depressive Symptomatology-Self-Report (QIDS-SR) total score
Time frame: From randomization to endpoint (Week 24)
The changes of Frequency, Intensity, and Burden of Side Effects-Rating (FIBSER)
The FIBSER is a self-report instrument assessing three domains of medication side effects within the past week
Time frame: From randomization to endpoint (Week 24)
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