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Adaptation of the Friendship Bench Intervention for HIV-infected Perinatal Women in Lilongwe (Periscope)

Primary Purpose

Human Immunodeficiency Virus, Perinatal Depression

Status
Completed
Phase
Not Applicable
Locations
Malawi
Study Type
Interventional
Intervention
Enhanced Friendship Bench
Enhanced Standard Care (Control)
Adapted Friendship Bench
Sponsored by
University of North Carolina, Chapel Hill
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Human Immunodeficiency Virus focused on measuring HIV, Depression

Eligibility Criteria

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

Women

Inclusion criteria:

  • HIV-infected, pregnant women initiating or re-initiating ART during antenatal care (ANC)
  • ≤30 weeks gestation to allow sufficient time for approximately 4 prenatal counseling sessions and approximately 2 postnatal counseling sessions.
  • Screened positive for depression with a score > 8 on the SRQ-20
  • At least 18 years of age

Exclusion criteria:

  • Women already successfully established on ART will be excluded because they are at a lower risk for disengagement from HIV care.

Sites / Locations

  • Mitundu Health Center
  • Lumbadzi Health Center
  • Nathenje Health Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Experimental

Arm Label

Enhanced Friendship Bench (EFB)

Enhanced Standard Care (ESC)

Adapted Friendship Bench (AFB)

Arm Description

Women seeking ANC services at 2 public health centers in Lilongwe, Malawi will be enrolled into this study arm during study recruitment. Individuals enrolled in this arm will be administered the Enhanced Friendship Bench intervention from date of enrollment through 6 months post-partum.

Women seeking ANC services at 2 public health centers in Lilongwe, Malawi will be enrolled into this study arm during study recruitment. Individuals enrolled in this arm will received the Enhanced Standard Care intervention from date of enrollment through 6 months post-partum.

Women seeking ANC services at 2 public health centers in Lilongwe, Malawi will be enrolled into this study arm during study recruitment. Individuals enrolled in this arm will be administered the Adapted Friendship Bench intervention from date of enrollment through 6 months post-partum.

Outcomes

Primary Outcome Measures

Intervention Feasibility- Number of Participants Enrolled in Each Arm
This measure of feasibility will be assessed as the number of women enrolled in each arm out of the desired total sample size of 92 women during the 16 month recruitment period.
Intervention Feasibility- Proportion of Women Retained in Each Study Arm at 6 Months Post-partum
The proportion of enrolled study participants that remain in their assigned study arm at 6-months post-partum.
Acceptability of Intervention- Proportion of Women Enrolled That Found Intervention Easy to Participate in
The proportion of women in the intervention arm (EFB) that were either "satisfied" or "highly satisfied" with the intervention as reported in the 6-month follow-up survey.
Fidelity to Intervention- Proportion of Observed Intervention Sessions Covering 80% of Intervention Checklist Items
Fidelity will be assessed by members of the Friendship Bench team (DHO or study psychiatrist), by using a checklist of intervention characteristics either during direct monitoring or using audio recording of up to 3 randomly chosen counseling sessions. Scoring either 'meeting expectations' or 'exceeding' expectations' on at least 80% of applicable checklist items during each session will be considered fidelity to the intervention protocol.

Secondary Outcome Measures

Composite Outcome: Proportion of Women Retained in HIV Care With Improved Depression
The investigator will assess a combined outcome at 6 months of whether a woman was retained in HIV care (defined as attending an HIV care appointment within the 30 days prior to the 6-month interview) and had ≥50% improvement in the Self-Reporting Questionnaire-20 (SRQ-20) score from baseline. The SRQ-20 was developed by the World Health Organization and has scores ranging from 0 to 20 and higher scores indicating a greater level of depression. Scores greater than or equal to 8 are typically considered indicative of a common mental disorder (CMD). This measure will capture the proportion of enrolled women with the composite outcome of interest described above.

Full Information

First Posted
October 25, 2019
Last Updated
August 10, 2023
Sponsor
University of North Carolina, Chapel Hill
Collaborators
National Institute of Mental Health (NIMH), Brown University, Ministry of Health, Malawi, University of Zimbabwe
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1. Study Identification

Unique Protocol Identification Number
NCT04143009
Brief Title
Adaptation of the Friendship Bench Intervention for HIV-infected Perinatal Women in Lilongwe
Acronym
Periscope
Official Title
Adaptation of the Friendship Bench Mental Health Intervention for HIV-infected Perinatal Women in Lilongwe (Periscope)
Study Type
Interventional

2. Study Status

Record Verification Date
August 2022
Overall Recruitment Status
Completed
Study Start Date
December 10, 2019 (Actual)
Primary Completion Date
August 31, 2022 (Actual)
Study Completion Date
August 31, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of North Carolina, Chapel Hill
Collaborators
National Institute of Mental Health (NIMH), Brown University, Ministry of Health, Malawi, University of Zimbabwe

4. Oversight

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

5. Study Description

Brief Summary
In many sub-Saharan African countries, the scale-up of lifelong antiretroviral treatment (ART) to all pregnant and breastfeeding women under Option B+ has the potential to radically improve maternal health and reduce mother-to-child HIV transmission. However, loss to HIV care after delivery has emerged as an important threat to the hoped-for impact of Option B+. Evidence suggests that one important contributor to postpartum loss to HIV care is perinatal depression (PND). In non-pregnant HIV-infected populations, depression has been linked to poor ART adherence, reduced engagement in care, and ultimately worse HIV clinical outcomes. Thus, interventions that integrate PND treatment with targeted support for HIV care retention are critical to the success of Option B+. The Friendship Bench is an evidence-based depression counseling intervention delivered by trained, supervised lay health workers. It is proven to reduce depression in the general population in low-resource settings, but has not been adapted to address PND, or enhanced to support engagement in HIV care. The Friendship Bench offers an ideal framework for integrating retention support into a proven depression treatment model. Our long-term goal is to adapt, test, and scale up resource-appropriate interventions to reduce PND and improve engagement in HIV care. The objective of this proposal is to lay the groundwork for an effectiveness trial by adapting the Friendship Bench intervention to address PND and support engagement in care among perinatal HIV-infected women and assessing the feasibility, acceptability, and fidelity of the adapted intervention in Lilongwe, Malawi. In-depth perspectives on PND and its role in engagement in care will be gathered from HIV-infected women with PND, healthcare providers, clinic directors, and Ministry of Health officials using qualitative interviews and focus groups. This formative research will be used to develop an intervention protocol adapted to the unique needs of HIV-infected women during the perinatal period (Adapted Friendship Bench) and further enhanced to support engagement in HIV care (Enhanced Friendship Bench). The Adapted and Enhanced Friendship Bench interventions will be compared to enhanced standard care in a 3-arm pilot study. Feasibility, acceptability, and fidelity will be assessed at 6 months postpartum, along with the interventions' preliminary effectiveness across several mental health and engagement in HIV care measures.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Human Immunodeficiency Virus, Perinatal Depression
Keywords
HIV, Depression

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
92 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Enhanced Friendship Bench (EFB)
Arm Type
Experimental
Arm Description
Women seeking ANC services at 2 public health centers in Lilongwe, Malawi will be enrolled into this study arm during study recruitment. Individuals enrolled in this arm will be administered the Enhanced Friendship Bench intervention from date of enrollment through 6 months post-partum.
Arm Title
Enhanced Standard Care (ESC)
Arm Type
Active Comparator
Arm Description
Women seeking ANC services at 2 public health centers in Lilongwe, Malawi will be enrolled into this study arm during study recruitment. Individuals enrolled in this arm will received the Enhanced Standard Care intervention from date of enrollment through 6 months post-partum.
Arm Title
Adapted Friendship Bench (AFB)
Arm Type
Experimental
Arm Description
Women seeking ANC services at 2 public health centers in Lilongwe, Malawi will be enrolled into this study arm during study recruitment. Individuals enrolled in this arm will be administered the Adapted Friendship Bench intervention from date of enrollment through 6 months post-partum.
Intervention Type
Behavioral
Intervention Name(s)
Enhanced Friendship Bench
Intervention Description
EFB will include the following: integrating problem solving therapy- based ART adherence support into existing counseling sessions and providing opportunities for participants to address HIV-specific concerns, such as stigma, disclosure, mother-to-child HIV transmission or other issues women identify during counseling sessions, and retention strategies to support engagement in care for HIV-infected women with PND. This intervention will include 4 individual prenatal and 2 group postnatal counseling sessions. To provide additional social support, one support session will be added, at which participants will be invited to bring a person of her choice who can be a support to her in managing both her HIV and/or depression. To assist women with receiving their medication during late pregnancy and postpartum, a trained psychosocial counselor will conduct up to 6 home visits. At each home visit, counselors will be able to deliver a participants' medications and conduct a counseling session.
Intervention Type
Other
Intervention Name(s)
Enhanced Standard Care (Control)
Intervention Description
Standard care for mental health in public facilities in Malawi includes options for basic supportive counseling by the primary provider or nurse, medication management by the primary provider, referral to the clinic psychiatric nurse or mental health clinic, or in more severe cases referral to the psychiatric units at tertiary care hospitals. For this study, standard care will be enhanced by a trained study research assistant who will provide mental health evaluation; brief supportive counseling; information, education, and support on common mental disorders; and (if indicated) facilitation of referral to the clinic's psychiatric nurse or mental health clinic. The study research assistant will have up to 3 follow-up contacts with the participant to assess whether she has followed up on recommended referrals or treatment plans and to assess whether any further outreach is indicated.
Intervention Type
Behavioral
Intervention Name(s)
Adapted Friendship Bench
Intervention Description
Adapted Friendship Bench (AFB): AFB will include the following: integrating problem solving therapy- based and antiretroviral therapy (ART) adherence support into existing counseling sessions and providing opportunities for participants to address HIV-specific concerns, such as stigma, disclosure, mother-to-child HIV transmission or other issues women identify during counseling sessions. AFB will include 4 individual prenatal counseling session and 2 group postnatal counseling sessions. No specific retention support will be provided, but participants may identify barriers to engagement in HIV care to address during their pre- or postnatal counseling sessions.
Primary Outcome Measure Information:
Title
Intervention Feasibility- Number of Participants Enrolled in Each Arm
Description
This measure of feasibility will be assessed as the number of women enrolled in each arm out of the desired total sample size of 92 women during the 16 month recruitment period.
Time Frame
Study enrollment period of approximately 16 months
Title
Intervention Feasibility- Proportion of Women Retained in Each Study Arm at 6 Months Post-partum
Description
The proportion of enrolled study participants that remain in their assigned study arm at 6-months post-partum.
Time Frame
6-months post-partum
Title
Acceptability of Intervention- Proportion of Women Enrolled That Found Intervention Easy to Participate in
Description
The proportion of women in the intervention arm (EFB) that were either "satisfied" or "highly satisfied" with the intervention as reported in the 6-month follow-up survey.
Time Frame
6 months post-partum
Title
Fidelity to Intervention- Proportion of Observed Intervention Sessions Covering 80% of Intervention Checklist Items
Description
Fidelity will be assessed by members of the Friendship Bench team (DHO or study psychiatrist), by using a checklist of intervention characteristics either during direct monitoring or using audio recording of up to 3 randomly chosen counseling sessions. Scoring either 'meeting expectations' or 'exceeding' expectations' on at least 80% of applicable checklist items during each session will be considered fidelity to the intervention protocol.
Time Frame
Entire study period (Study baseline through 6 months post-partum)
Secondary Outcome Measure Information:
Title
Composite Outcome: Proportion of Women Retained in HIV Care With Improved Depression
Description
The investigator will assess a combined outcome at 6 months of whether a woman was retained in HIV care (defined as attending an HIV care appointment within the 30 days prior to the 6-month interview) and had ≥50% improvement in the Self-Reporting Questionnaire-20 (SRQ-20) score from baseline. The SRQ-20 was developed by the World Health Organization and has scores ranging from 0 to 20 and higher scores indicating a greater level of depression. Scores greater than or equal to 8 are typically considered indicative of a common mental disorder (CMD). This measure will capture the proportion of enrolled women with the composite outcome of interest described above.
Time Frame
6 months post-partum
Other Pre-specified Outcome Measures:
Title
Proportion of Women Reporting a Score Greater Than or Equal to 8 on the Self-Reporting Questionnaire-20 (SRQ-20)
Description
The proportion of women in each arm that score greater than or equal to 8 on the Self-Reporting Questionnaire-20 at a study visit approximately 6-months post-partum. The SRQ-20 was developed by the World Health Organization and has scores ranging from 0 to 20 and higher scores indicating a greater level of depression. Scores greater than or equal to 8 are typically considered indicative of a common mental disorder (CMD).
Time Frame
6 months post-partum
Title
Proportion of Women Retained in HIV Care
Description
The proportion of women who attended at least 1 HIV care appointment within 30-days prior to the 6-month interview.
Time Frame
6 months post-partum
Title
Proportion of Women Virally Suppressed
Description
The proportion of women in each arm with an HIV viral load of <1,000 copies/mL
Time Frame
6 months post partum
Title
The Proportion of Women Whose Infants Received an HIV Viral Load Test
Description
The proportion of women in each arm whose infants had received an HIV viral load test by the time of a study visit approximately 6-months post-partum
Time Frame
6 months post partum

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
The investigators are recruiting pregnant women with perinatal depression
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Women Inclusion criteria: HIV-infected, pregnant women initiating or re-initiating ART during antenatal care (ANC) ≤30 weeks gestation to allow sufficient time for approximately 4 prenatal counseling sessions and approximately 2 postnatal counseling sessions. Screened positive for depression with a score > 8 on the Self-Reporting Questionnaire 20-item (SRQ-20) At least 18 years of age Exclusion criteria: Women already successfully established on ART will be excluded because they are at a lower risk for disengagement from HIV care.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Brian Pence, PhD
Organizational Affiliation
University of North Carolina, Chapel Hill
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mitundu Health Center
City
Lilongwe
State/Province
Lilogwe
Country
Malawi
Facility Name
Lumbadzi Health Center
City
Lilongwe
Country
Malawi
Facility Name
Nathenje Health Center
City
Lilongwe
Country
Malawi

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
The investigators do not intend to share individual participant data (IPD) with other researchers.

Learn more about this trial

Adaptation of the Friendship Bench Intervention for HIV-infected Perinatal Women in Lilongwe

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