Depression Clinical Trial
— MEDIUMOfficial title:
Integrating Treatment for Mental Disorders in Methadone Clinics in Ukraine
Verified date | May 2024 |
Source | Ukrainian Institute on Public Health Policy |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The MEDIUM study (U01DA045384) is a cluster-randomized trial based in Ukraine. The main goal of the study is to test the implementation strategies for mental health treatment services in OAT clinics. The study enrolled 12 OAT clinics from 12 geographically and epidemiologically diverse regions and randomized them 1:1:1 to three implementation arms: standard of care (SoC), ECHO facilitation, and ECHO plus pay-for-performance (P4P) incentives. Project ECHO, is an evidence-based telehealth intervention, connecting clinicians with national experts for short thematic didactic sessions and case discussions. All sites are provided with a modified Screening, Brief Intervention and Referral to Treatment (mSBIRT) intervention manual for mental disorders and regular supply of two selective serotonin reuptake inhibitors (SSRI) medications. All current and new patients at participating sites (N~2000 at study start) are automatically eligible for SSRI prescription. The main outcomes of the study are the elements of mental health continuum of care (screening, diagnosis, treatment and retention). These outcomes are assessed in the entire patient population using de-personalized data extracted from the electronic medical record system. A sub-sample of patients (N=1,350) was recruited into a cohort and consented to assess prevalence and severity of mental disorders, various factors related to the uptake of and retention in mental health treatment (addiction severity, other substance use, co-morbidities), as well as other important covariates. These assessments are done at baseline, 6, 12, 18 and 24 months after enrollment.
Status | Active, not recruiting |
Enrollment | 1350 |
Est. completion date | May 31, 2025 |
Est. primary completion date | January 31, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - All patients receiving OAT at participating sites Exclusion Criteria: - Not willing to participate - Unable to sign informed consent |
Country | Name | City | State |
---|---|---|---|
Ukraine | Ivano-Frankivsk regional narcological dispensary | Ivano-Frankivs'k | |
Ukraine | Kropyvnitsky regional narcological dispensary | Kropyvnytskyi | Kirovohrad |
Ukraine | Kryvyi Rig psycho-neurological dispensary | Kryvyi Rih | Dnipropetrovsk |
Ukraine | Kyiv city narcological clinic 'Sociotherapia' | Kyiv | |
Ukraine | Mykolaiv City Hospital #5 | Mykolayiv | |
Ukraine | Mykolaiv regional narcological dispensary | Mykolayiv | Mykolaiv |
Ukraine | Dnipropetrovsk narcological dispensary | Pavlograd | Dnipropetrovsk |
Ukraine | Ternopil regional narcological dispensary | Ternopil' | Ternopil |
Ukraine | Vinnitsia regional narcological dispensary 'Sociotherapia' | Vinnytsia |
Lead Sponsor | Collaborator |
---|---|
Ukrainian Institute on Public Health Policy | Alliance for Public Health, Yale University |
Ukraine,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Proportion of patients screened for depression by clinical staff using Patient Health Questionnaire-2 (PHQ-2) | Site-level indicator | 30 months (August 2019 - February 2022) | |
Primary | Proportion of patients assessed by physician using Montgomery-Asberg Depression Rating Scale (MADRS) and motivated for treatment | Site-level indicator | 30 months (August 2019 - February 2022) | |
Primary | Proportion of patients initiated on Selective serotonin reuptake inhibitors (SSRIs) | Site-level indicator | 30 months (August 2019 - February 2022) | |
Primary | Proportion of patients retained on Selective serotonin reuptake inhibitors (SSRIs) | Site-level indicator | 30 months (August 2019 - February 2022) | |
Secondary | Number of participants who continue opioid agonist treatment at the assessment time point | Retention on opioid agonist treatment | 3, 6, 12, 18 and 24 months after enrollment for each patient | |
Secondary | Psychiatric Quality of Life (SF-12 mental component score) changes over time | Change in the mental component score of the Short-Form Health Survey version 2 (SF-12v2) scale (0-100, higher means better health). | 3, 6, 12, 18 and 24 months after enrollment for each patient |
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