Depressive Symptoms Clinical Trial
— DepCareOfficial title:
A Randomized Control Trial of a Multi-level Theoretical Approach to Enhancing Patient Engagement in Primary Care Settings Sustaining Collaborative Depression Care (Transform DepCare)
The purpose of this study is to examine the effectiveness of a multi-level intervention - centered around a web-application that facilitates depression screening, automated shared decision making (SDM), patient activation, and psychoeducation - on mental health treatment optimization among patients with elevated depressive symptoms with or without co-morbid anxiety receiving care in primary care clinics that offer collaborative care. The objectives of the study include: Leveraging user centered design to refine an electronic SDM (eSDM) tool (aim 1), and assessing the effect of the eSDM tool on provider behavior (aim 2) and on patient enrollment in depression treatment (aim 3).
Status | Recruiting |
Enrollment | 266 |
Est. completion date | December 1, 2024 |
Est. primary completion date | December 1, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - English or Spanish Speaking - = 18 years of age - Elevated depressive symptoms Elevated Patient Health Questionnaire (PHQ)-9 >=10 Elevated PHQ-9 >=5 and Generalized Anxiety Disorder (GAD)-7 >= 10 Exclusion Criteria: - Under the care of a psychiatrist or depression collaborative care manager in the prior 3 months - Diagnosis of psychosis or schizophrenia - Diagnosis of bipolar disorder - Dementia or severe cognitive impairment - History of coronary heart disease - Pregnancy - Dementia or severe cognitive impairment |
Country | Name | City | State |
---|---|---|---|
United States | Columbia University Irving Medical Center/New York Presbyterian Hospital | New York | New York |
Lead Sponsor | Collaborator |
---|---|
Columbia University | Agency for Healthcare Research and Quality (AHRQ) |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Total proportion of patients who initiate or optimize depression treatment | The proportion of patients who initiate or optimize depression treatment, defined as those with at least 1 mental health visit or antidepressant fill during the 4 months following enrollment. Hypothesis 1: this proportion will be greater for patients of providers in the DepCare arm than for the Enhanced Usual Care arm | During 4 months post-index visit | |
Secondary | Proportion of patients whose providers take action to optimize depression treatment | The proportion of patients whose providers take action to optimize their patients' depression treatment at the index visit (baseline), defined as placing a mental health referral for collaborative care or other mental health services; initiating, intensifying, switching and/or combining antidepressant medications; and/or providing depression management counseling [i.e., on adherence to treatment regimen]. Hypothesis 2: this proportion will be greater for the DepCare arm than for the Enhanced Usual Care arm. | Baseline | |
Secondary | Change in proportion of patients receiving any depression treatment | Change from baseline in the proportion of patients receiving any treatment for depression, defined as filling an antidepressant and/or attending one or more mental health visits during the 4 months following enrollment. Hypothesis 3: This proportion will be greater for the DepCare arm than for the Enhanced Usual Care arm. | 4 months pre-Index Visit, 4 months post-index visit | |
Secondary | Proportion of patients with at least 2 mental health visits | The proportion of patients with at least 2 mental health visits (i.e., with a mental health specialist). Hypothesis 4: This proportion will be greater for the DepCare arm than for the Enhanced Usual Care arm. | During 6 months post-index visit | |
Secondary | Proportion of patients with at least 2 antidepressant fills | The proportion of patients with at least 2 antidepressant fills. Hypothesis 5: This proportion will be greater for the DepCare arm than for the Enhanced Usual Care arm. | During 6 months post-index visit | |
Secondary | Mean decisional conflict scale | Mean decisional conflict (measures personal perceptions of uncertainty around choosing among treatment option, 10 items, range 0-100, higher score indicates greater conflict) of patients. Hypothesis 5: the mean decisional conflict will be lower for the DepCare arm than for the Enhanced Usual Care arm. | Baseline |
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