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Measurement-based Care for Depression in Resource-Poor Settings (MBC)

Primary Purpose

Major Depression

Status
Completed
Phase
Phase 4
Locations
Haiti
Study Type
Interventional
Intervention
Fluoxetine
Enhanced Usual Care
Sponsored by
Florida International University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Major Depression

Eligibility Criteria

18 Years - 59 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • (1) >18, but <60 years of age; 2) able to provide informed consent; 3) documentation of HIV seropositivity; 4) ART-naïve scheduled to begin ART within 1 month; 5) total score of 10 or higher on the PHQ-9, indicating likely major depression; 6) confirmed for major depression on the MINI (Mini International Neuropsychiatric Interview);

Exclusion Criteria:

  • (7) currently cognitively impaired, as determined by the MINI, since cognitive impairment may compromise the ability to comprehend and participate in the assessment and intervention; 8) bipolar disorder, psychosis, or current need for inpatient psychiatric hospitalization; 9) currently pregnant or enrolled in the GHESKIO PMTCT (Prevention of mother to child transmission) program.

Sites / Locations

  • GHESKIO Centers

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Measurement Based Care

Enhanced Usual Care

Arm Description

Fluoxetine prescribed and dispensed beginning at 10 mg daily; side effects and symptoms monitored biweekly; dosage increased to 20 mg., then by 20 mg. increments according to protocol algorithm based on PHQ-9 score to a maximum dose of 60 mg.

Depression symptoms monitored at 3 month interval; results from PHQ-9 available to ART clinic physicians.

Outcomes

Primary Outcome Measures

Remission of Depression
PHQ-9 less than 5

Secondary Outcome Measures

ART adherence - viral suppression
Improvement in Viral Load measurements
ART adherence - immune functioning
Improvement in CD4 measurements
Total treatment cost from the health center perspective
Inform a mental health intervention model for ART networks in low-and-middle income

Full Information

First Posted
September 24, 2016
Last Updated
November 29, 2016
Sponsor
Florida International University
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1. Study Identification

Unique Protocol Identification Number
NCT02916238
Brief Title
Measurement-based Care for Depression in Resource-Poor Settings
Acronym
MBC
Official Title
Measurement-based Care for Depression in Resource-Poor Settings
Study Type
Interventional

2. Study Status

Record Verification Date
November 2016
Overall Recruitment Status
Completed
Study Start Date
February 2014 (undefined)
Primary Completion Date
November 2016 (Actual)
Study Completion Date
November 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Florida International University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Depression is often the most prevalent mental health problem among people living with HIV (PLWH) worldwide, and if not adequately treated, it may impair response to antiretroviral treatment (ART) and the ability of individuals to adhere to medications and healthy behavior. Most patients with depression receiving ART in the poorest countries of the world are left untreated because no systematic approach or expertise is available. This study adapts an evidence-based model of depression care (Measurement-Based Care - MBC) using auxiliary HIV clinic staff, and tests feasibility and assesses costs among HIV positive patients beginning ART in Port-au-Prince, Haiti.
Detailed Description
This developmental and exploratory study develops and tests a scalable model for the diagnosis and treatment of depression among HIV-infected patients initiating antiretroviral therapy (ART) in resource-poor settings. The investigators conduct a pilot test of the measurement-based care (MBC) approach to intervening, task shifting, and managing depression, which was adapted for use with auxiliary personnel who support HIV physicians in algorithm-guided antidepressant treatment. This intervention is based on the MBC approach developed by Pence, and conducted in HIV clinical sites in the US and Africa. The investigators adapted and tested an auxiliary-driven model, MBC-Aux, which is the first study of this approach with auxiliary personnel in a resource- poor country and its ART system. The study was conducted at the GHESKIO Centers in Port-au-Prince, Haiti, which is responsible for 50% of the ART population in Haiti. The investigators conducted a formative study of psychosocial factors related to depression and antidepressant medication in Aim 1, adapted the MBC depression medication and monitoring algorithm for use by auxiliary personnel at GHESKIO in Aim 2 and conducted a pre-test of procedures, and piloted the resulting MBC-Aux adaptation in Aim 3 compared to Enhanced Usual Care. The investigators also evaluated feasibility and cost. Although they are very safe medications, use of antidepressants in MBC-Aux, like use of all pharmacologic agents, incurs some measurable risk of mild, moderate and rare but severe side effects. Risks were explained to participants receiving antidepressant treatment and MBC-Aux includes systematic monitoring of participants taking these medications. This R21 developmental and exploratory study will produce the first systematic formative work of psychosocial factors related to depression in Haiti, and is the first to apply and test the MBC approach with auxiliary personnel.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Major Depression

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
140 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Measurement Based Care
Arm Type
Experimental
Arm Description
Fluoxetine prescribed and dispensed beginning at 10 mg daily; side effects and symptoms monitored biweekly; dosage increased to 20 mg., then by 20 mg. increments according to protocol algorithm based on PHQ-9 score to a maximum dose of 60 mg.
Arm Title
Enhanced Usual Care
Arm Type
Active Comparator
Arm Description
Depression symptoms monitored at 3 month interval; results from PHQ-9 available to ART clinic physicians.
Intervention Type
Drug
Intervention Name(s)
Fluoxetine
Other Intervention Name(s)
Prozac
Intervention Description
Fluoxetine prescribed and dispensed beginning at 10 mg daily; side effects and symptoms monitored biweekly; dosage increased to 20 mg., then by 20 mg. increments according to protocol algorithm based on PHQ-9 score to a maximum dose of 60 mg.
Intervention Type
Behavioral
Intervention Name(s)
Enhanced Usual Care
Intervention Description
Depression symptoms monitored at 3 month intervals; results from PHQ-9 available to ART clinic physicians.
Primary Outcome Measure Information:
Title
Remission of Depression
Description
PHQ-9 less than 5
Time Frame
6 months
Secondary Outcome Measure Information:
Title
ART adherence - viral suppression
Description
Improvement in Viral Load measurements
Time Frame
6 months
Title
ART adherence - immune functioning
Description
Improvement in CD4 measurements
Time Frame
6 months
Title
Total treatment cost from the health center perspective
Description
Inform a mental health intervention model for ART networks in low-and-middle income
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
59 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: (1) >18, but <60 years of age; 2) able to provide informed consent; 3) documentation of HIV seropositivity; 4) ART-naïve scheduled to begin ART within 1 month; 5) total score of 10 or higher on the PHQ-9, indicating likely major depression; 6) confirmed for major depression on the MINI (Mini International Neuropsychiatric Interview); Exclusion Criteria: (7) currently cognitively impaired, as determined by the MINI, since cognitive impairment may compromise the ability to comprehend and participate in the assessment and intervention; 8) bipolar disorder, psychosis, or current need for inpatient psychiatric hospitalization; 9) currently pregnant or enrolled in the GHESKIO PMTCT (Prevention of mother to child transmission) program.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jessy G. Dévieux, Ph.D.
Organizational Affiliation
Florida International University
Official's Role
Principal Investigator
Facility Information:
Facility Name
GHESKIO Centers
City
Port-au-Prince
Country
Haiti

12. IPD Sharing Statement

Plan to Share IPD
Yes

Learn more about this trial

Measurement-based Care for Depression in Resource-Poor Settings

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