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Comparative Trial of Antidepressant Treatment Models in HIV Care in Uganda (INDEPTH-Uganda)

Primary Purpose

Depression

Status
Completed
Phase
Phase 4
Locations
Uganda
Study Type
Interventional
Intervention
antidepressant therapy
Sponsored by
RAND
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Depression focused on measuring depression, Uganda, HIV, task-shifting, condom use, adherence

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • age 18 years or above
  • screens positive for depression (scores > 2 on PHQ-2)
  • medically stable
  • client at the HIV clinic (and hence, HIV positive)

Exclusion Criteria:

  • active acute opportunistic infection
  • about to start HIV antiretroviral therapy or started antiretroviral therapy within past 4 weeks

Sites / Locations

  • health care facilities receiving technical assistance from Mildmay Uganda

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Clinical acumen

Protocolized Arm

Arm Description

Depression diagnosis and antidepressant treatment provided based on clinical acumen of primary care providers trained to provide depression care.

Structured, algorithm-based protocol that guides depression diagnosis and antidepressant treatment

Outcomes

Primary Outcome Measures

Depression diagnostic evaluation
Whether or not the Patient Health Questionnaire (PHQ-9) was administered to assess severity of depression
Antidepressant prescription
Whether or not antidepressants were prescribed; this variable will be analyzed among the subset of patients categorized as depressed based on PHQ-9 > 9
Depressive symptoms
depressive symptoms present at Month 6 and Month 12 (in comparison to baseline) to assess treatment response; PHQ-9 will be used to measure depressive symptoms

Secondary Outcome Measures

Consistent condom use
A single likert scale item will be used to assess condom use in the past month; a single item will also be used to assess whether condom was used during last event of sexual intercourse
ART adherence
single variable to rate adherence to ART over the past month on scale of 0-100

Full Information

First Posted
February 3, 2014
Last Updated
October 2, 2015
Sponsor
RAND
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1. Study Identification

Unique Protocol Identification Number
NCT02056106
Brief Title
Comparative Trial of Antidepressant Treatment Models in HIV Care in Uganda
Acronym
INDEPTH-Uganda
Official Title
Task Shifting Model of Depression Treatment to Unleash HIV Public Health Benefits
Study Type
Interventional

2. Study Status

Record Verification Date
October 2015
Overall Recruitment Status
Completed
Study Start Date
January 2013 (undefined)
Primary Completion Date
December 2014 (Actual)
Study Completion Date
December 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
RAND

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study compares two models for implementing antidepressant treatment in 10 HIV clinics in Uganda. Using a cluster randomization, 5 clinics implement a task-shifting, protocolized model, and 5 others rely on clinical acumen. The protocolized model includes (1) routine depression screening at each clinic visit for all adult patients by trained expert patients at triage, (2) training nurses to diagnose depression and prescribe and monitor antidepressant treatment using an algorithm-based protocol, and (3) monthly supervision and monitoring by hired study psychiatrists. The clinical acumen model also includes routine depression screening and ongoing supervision, but it relies on the clinical acumen of trained primary care providers to further evaluate and treat patients who show signs of depression at screening, as opposed to a structured protocol. The primary aim is to test the hypothesis that the nurse-driven protocolized model will result in greater uptake of antidepressant treatment and better quality of depression care outcomes. The study will also test the hypotheses that treatment of depression results in improved HIV treatment adherence, work functioning and consistent condom use.
Detailed Description
The study evaluates a task-shifting approach to depression treatment that uses an algorithm-based, nurse-driven model for managing antidepressant treatment in 10 Ugandan HIV clinics. The model will include (1) case identification facilitated by routine depression screening at each clinic visit for all patients, (2) training nurses to assist primary care providers in implementing antidepressant treatment by performing the initial evaluation, monitoring symptoms and side effects, and making algorithm-based dose recommendations, and (3) layers of supervision and monitoring by psychiatric specialists to ensure safety and quality of care. This model will be implemented at 5 randomly selected clinics (protocolized arm), while 5 other clinics will be selected to also use routine depression screening but will rely on primary care providers to decide whether to further evaluate and treat depression (clinical acumen arm). At each site, random samples of 150 patients (total n=1500) who have screened positive for possible depression will be followed for 12 months. We will compare the two arms on depression evaluation, uptake of antidepressant treatment, and change in depression (treatment response). We will also examine the relationship between change in depression and key economic and public health outcomes (e.g. work status, condom use, HIV treatment adherence).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression
Keywords
depression, Uganda, HIV, task-shifting, condom use, adherence

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
1252 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Clinical acumen
Arm Type
Active Comparator
Arm Description
Depression diagnosis and antidepressant treatment provided based on clinical acumen of primary care providers trained to provide depression care.
Arm Title
Protocolized Arm
Arm Type
Active Comparator
Arm Description
Structured, algorithm-based protocol that guides depression diagnosis and antidepressant treatment
Intervention Type
Drug
Intervention Name(s)
antidepressant therapy
Primary Outcome Measure Information:
Title
Depression diagnostic evaluation
Description
Whether or not the Patient Health Questionnaire (PHQ-9) was administered to assess severity of depression
Time Frame
baseline, Month 6, Month 12
Title
Antidepressant prescription
Description
Whether or not antidepressants were prescribed; this variable will be analyzed among the subset of patients categorized as depressed based on PHQ-9 > 9
Time Frame
baseline, Month 6, Month 12
Title
Depressive symptoms
Description
depressive symptoms present at Month 6 and Month 12 (in comparison to baseline) to assess treatment response; PHQ-9 will be used to measure depressive symptoms
Time Frame
past 2 weeks at Month 6 and Month 12
Secondary Outcome Measure Information:
Title
Consistent condom use
Description
A single likert scale item will be used to assess condom use in the past month; a single item will also be used to assess whether condom was used during last event of sexual intercourse
Time Frame
past 6 months prior to baseline, Month 6, Month 12
Title
ART adherence
Description
single variable to rate adherence to ART over the past month on scale of 0-100
Time Frame
past month prior to baseline, Month 6 and Month 12

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age 18 years or above screens positive for depression (scores > 2 on PHQ-2) medically stable client at the HIV clinic (and hence, HIV positive) Exclusion Criteria: active acute opportunistic infection about to start HIV antiretroviral therapy or started antiretroviral therapy within past 4 weeks
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Glenn Wagner, PhD
Organizational Affiliation
RAND
Official's Role
Principal Investigator
Facility Information:
Facility Name
health care facilities receiving technical assistance from Mildmay Uganda
City
Wakiso, Mpigi, Luwero, Mityana districts
Country
Uganda

12. IPD Sharing Statement

Citations:
PubMed Identifier
27167852
Citation
Wagner GJ, Ngo V, Goutam P, Glick P, Musisi S, Akena D. A Structured Protocol Model of Depression Care versus Clinical Acumen: A Cluster Randomized Trial of the Effects on Depression Screening, Diagnostic Evaluation, and Treatment Uptake in Ugandan HIV Clinics. PLoS One. 2016 May 11;11(5):e0153132. doi: 10.1371/journal.pone.0153132. eCollection 2016.
Results Reference
derived
PubMed Identifier
24962086
Citation
Wagner GJ, Ngo V, Glick P, Obuku EA, Musisi S, Akena D. INtegration of DEPression Treatment into HIV Care in Uganda (INDEPTH-Uganda): study protocol for a randomized controlled trial. Trials. 2014 Jun 25;15:248. doi: 10.1186/1745-6215-15-248.
Results Reference
derived

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Comparative Trial of Antidepressant Treatment Models in HIV Care in Uganda

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