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Project SOAR-Mental Health Malawi: Depression and HIV Integration

Primary Purpose

Depression, HIV/AIDS

Status
Completed
Phase
Not Applicable
Locations
Malawi
Study Type
Interventional
Intervention
Depression Treatment
Sponsored by
University of North Carolina, Chapel Hill
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Depression focused on measuring Implementation Science, Malawi

Eligibility Criteria

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

Inclusion Criteria:

  • Adult (≥18 years)
  • HIV-infected
  • Newly initiating antiretroviral treatment at one of the program sites
  • Screened for depression

Exclusion Criteria:

• None

Sites / Locations

  • Area 18 Clinic
  • Area 25 Clinic

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Screening Phase (Pre) Group

Treatment Phase (Post) Group

Arm Description

Patients who screen positive on the PHQ-9 for depression during the "pre" period will comprise the comparison group. Participants will receive "standard of care" depression treatment at the providers discretion.

Patients who screen positive during on the PHQ-9 for depression during the "post" period will comprise the active group. Participants will receive the depression treatment intervention in the form of anti-depressants and/or problem solving therapy (PST) based on their PHQ-9 score.

Outcomes

Primary Outcome Measures

Proportion of participants who are retained in care
Retention in care is defined as attending sufficient HIV appointments to maintain ART supply through the first 6 months on ART.
Proportion of participants who are virally suppressed
Viral suppression is defined as HIV RNA viral load of <1,000 copies/mL. Viral loads are measured approximately 6 months after ART initiation.

Secondary Outcome Measures

Proportion of participants who achieve depression remission (PHQ-9 score less than 5)
Depression remission is defined as scoring less than 5 on the PHQ-9 approximately 6 months after ART initiation. The PHQ-9 is a self-report questionnaire designed to assess depression through nine questions that come directly from the DSM-IV signs and symptoms of major depression. The 9 items describe problems associated with depression, and participants must rate how often the patient has been bothered by the problems in the last 2 weeks on a 0-3 scale. The scores are summed for a total depression score, ranging from 0-27, with 0-4 being minimum and indicating no depressive symptoms, 5-9 mild depression, 10-14 moderate depression, 15-19 moderately severe depression, and 20-27 severe depression. Depressive symptoms will be measured with the PHQ-9 at baseline through approximately 6 months after ART initiation.
Proportion of scheduled ART visits attended
ART visit attendance is defined as attending scheduled ART appointments over the first 6 months on ART.

Full Information

First Posted
June 1, 2018
Last Updated
May 30, 2023
Sponsor
University of North Carolina, Chapel Hill
Collaborators
United States Agency for International Development (USAID)
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1. Study Identification

Unique Protocol Identification Number
NCT03555669
Brief Title
Project SOAR-Mental Health Malawi: Depression and HIV Integration
Official Title
UNCPM 21609 Project SOAR Mental Health: Evaluation of the Impact of a Depression Treatment Program on Mental Health and HIV Care Outcomes in Malawi
Study Type
Interventional

2. Study Status

Record Verification Date
June 2019
Overall Recruitment Status
Completed
Study Start Date
April 24, 2017 (Actual)
Primary Completion Date
May 31, 2019 (Actual)
Study Completion Date
May 31, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of North Carolina, Chapel Hill
Collaborators
United States Agency for International Development (USAID)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Depression is highly prevalent among people living with HIV (PLHIV) in Malawi and elsewhere in sub-Saharan Africa (SSA). Besides its high prevalence, depression likely represents an important barrier to consistent HIV care engagement and long-term viral suppression. However, the potential for depression treatment to improve HIV care outcomes has received little attention in the region, in part because of limited mental health infrastructure. In this study, the investigators will evaluate the impact of a depression treatment program integrated within existing HIV clinics on depression response, retention in HIV care, and viral suppression. It is expected that this evaluation will yield important evidence on the impact of depression treatment integrated with HIV care for improving HIV care and mental health outcomes in Malawi.
Detailed Description
Study population: The evaluation will abstract screening data for adult (≥18 years old) patients newly initiating antiretroviral therapy (ART) who are screened for depression at the two clinics before and after the integration of the depression treatment program, and additional treatment and outcome data for those patients who screen positive for depression. Study Size: Across the two clinics, the investigators expect to abstract depression screening data for approximately 2,300 patients. The investigators expect to abstract further treatment and outcome data for approximately 640 patients who screen positive for mild, moderate, or severe depression. Study Duration: Evaluation and dissemination activities will last two years. Study Evaluation: To evaluate the impact of the mental health treatment program on HIV care outcomes, the investigators will collect data on HIV appointment adherence and viral load at 6 months following ART initiation. To evaluate the impact of the mental health treatment program on mental health outcomes the investigators will collect data on depression symptoms at baseline through 6 months following ART initiation. Study Design Overview: The study will employ a pre-post design in two HIV clinics in Lilongwe to evaluate the impact of integrating the depression treatment program within existing clinic operations on HIV and mental health outcomes. The investigators will use existing medical records and the depression patient registry maintained by the Ministry of Health-run clinics to abstract routinely collected clinical data. Using these data, the investigators will compare mental health and HIV outcomes before and after the integration of the depression treatment program. Depressive symptoms will be measured with the Patient Health Questionnaire 9 (PHQ-9). The PHQ-9 is a self-report questionnaire designed to assess depression through nine questions that come directly from the Diagnostic and Statistical Manual of Mental Disorders, 4th Edition (DSM-IV) signs and symptoms of major depression. Additionally, the investigators will conduct short qualitative interviews with clinic and Ministry of Health staff about the integration of the depression screening and treatment program and with patients on their understanding of depression and satisfaction with depression screening and treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression, HIV/AIDS
Keywords
Implementation Science, Malawi

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Sequential Assignment
Model Description
The investigators will employ a multiple baseline evaluation design in two clinics to evaluate the impact of depression treatment on HIV outcomes. Patients who screen positive for depression using PHQ-9 during the "pre" period will comprise the comparison group, while patients who screen positive during the "post" period will comprise the active group.
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
2082 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Screening Phase (Pre) Group
Arm Type
No Intervention
Arm Description
Patients who screen positive on the PHQ-9 for depression during the "pre" period will comprise the comparison group. Participants will receive "standard of care" depression treatment at the providers discretion.
Arm Title
Treatment Phase (Post) Group
Arm Type
Experimental
Arm Description
Patients who screen positive during on the PHQ-9 for depression during the "post" period will comprise the active group. Participants will receive the depression treatment intervention in the form of anti-depressants and/or problem solving therapy (PST) based on their PHQ-9 score.
Intervention Type
Other
Intervention Name(s)
Depression Treatment
Intervention Description
The depression treatment program combines measurement-based antidepressant treatment with PST with clinical response appropriate to the level of depressive severity. Patients scoring 0-4 on the PHQ-9, indicating no depression, receive no treatment. Patients scoring 5-9 on the PHQ-9, indicating mild depressive symptoms that likely are not a full major depressive episode, are offered PST. Patients scoring 10 or above on the PHQ-9, indicating moderate-to-severe depressive symptoms, are first offered anti-depressants. For this group, PST will be an alternative or augmentation option for those who do not tolerate or respond to antidepressant treatment. All patients' depressive severity is monitored with the option of modifying their treatment plan if their symptoms worsen or do not improve.
Primary Outcome Measure Information:
Title
Proportion of participants who are retained in care
Description
Retention in care is defined as attending sufficient HIV appointments to maintain ART supply through the first 6 months on ART.
Time Frame
6 months after ART initiation
Title
Proportion of participants who are virally suppressed
Description
Viral suppression is defined as HIV RNA viral load of <1,000 copies/mL. Viral loads are measured approximately 6 months after ART initiation.
Time Frame
6 months after ART initiation
Secondary Outcome Measure Information:
Title
Proportion of participants who achieve depression remission (PHQ-9 score less than 5)
Description
Depression remission is defined as scoring less than 5 on the PHQ-9 approximately 6 months after ART initiation. The PHQ-9 is a self-report questionnaire designed to assess depression through nine questions that come directly from the DSM-IV signs and symptoms of major depression. The 9 items describe problems associated with depression, and participants must rate how often the patient has been bothered by the problems in the last 2 weeks on a 0-3 scale. The scores are summed for a total depression score, ranging from 0-27, with 0-4 being minimum and indicating no depressive symptoms, 5-9 mild depression, 10-14 moderate depression, 15-19 moderately severe depression, and 20-27 severe depression. Depressive symptoms will be measured with the PHQ-9 at baseline through approximately 6 months after ART initiation.
Time Frame
6 months after ART initiation
Title
Proportion of scheduled ART visits attended
Description
ART visit attendance is defined as attending scheduled ART appointments over the first 6 months on ART.
Time Frame
6 months after ART initiation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult (≥18 years) HIV-infected Newly initiating antiretroviral treatment at one of the program sites Screened for depression Exclusion Criteria: • None
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Brian Pence, PhD, MPH
Organizational Affiliation
UNC Gillings School of Global Public Health
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Michael Udedi, MBA MPhil
Organizational Affiliation
Malawi Ministry of Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
Area 18 Clinic
City
Lilongwe
Country
Malawi
Facility Name
Area 25 Clinic
City
Lilongwe
Country
Malawi

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
31242877
Citation
Udedi M, Stockton MA, Kulisewa K, Hosseinipour MC, Gaynes BN, Mphonda SM, Pence BW. The effectiveness of depression management for improving HIV care outcomes in Malawi: protocol for a quasi-experimental study. BMC Public Health. 2019 Jun 26;19(1):827. doi: 10.1186/s12889-019-7132-3.
Results Reference
derived
PubMed Identifier
30064418
Citation
Udedi M, Stockton MA, Kulisewa K, Hosseinipour MC, Gaynes BN, Mphonda SM, Mwagomba BM, Mazenga AC, Pence BW. Integrating depression management into HIV primary care in central Malawi: the implementation of a pilot capacity building program. BMC Health Serv Res. 2018 Jul 31;18(1):593. doi: 10.1186/s12913-018-3388-z.
Results Reference
derived

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Project SOAR-Mental Health Malawi: Depression and HIV Integration

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