- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06659315
Prevention of Mother-to-child Transmission (PMTCT) Among Women Experiencing Depression in Malawi
Addressing Perinatal Depression and PMTCT Adherence in Malawi: A Couple-Based Approach
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Although prevention of mother-to-child transmission of HIV (PMTCT) services are widely available, 140,000 infants contracted HIV in 2021 and the majority were in sub-Saharan Africa (SSA). Urgent attention is needed to address poor engagement in PMTCT care with more than half of mothers disengaged from care by six months postpartum. Perinatal depression (PD) is a robust predictor of poor engagement in HIV care and suboptimal PMTCT adherence-defined as adherence to antiretroviral therapy (ART), infant prophylaxis and testing, and exclusive breastfeeding. Few PD interventions have been developed to address PMTCT in SSA and none have involved male partners, who are often major sources of financial and emotional support. Nor have interventions targeted the couple dynamics that can influence the mother's experience of PD and ability to access PMTCT. This project aims to fill this gap by developing and evaluating a problem-solving therapy (PST) intervention with perinatal women and their male partners to reduce PD symptoms and improve adherence to PMTCT in Malawi.
Pregnancy and postpartum are challenging times for couples with the stress of a new child, rising food expenses and nutritional demands, potential for couple conflict with new stressors, and less opportunity for connection and intimacy-all of which are amplified in the presence of PD. Among perinatal women with HIV in Kenya, investigators found that women's mental health and adherence to PMTCT was worsened by intimate partner violence (IPV) but positively affected by social support from partners, including food support during pregnancy and the breastfeeding period. In Malawi, investigators found that women in higher functioning relationships (e.g., better intimacy, communication) reported lower levels of depression, whereas women who reported IPV had higher rates of depression. Together, this suggests that dyadic processes such as support, conflict, and communication are central for women's experience of depression and for PMTCT. However, most PD interventions have focused on women alone rather than the dyad, which may explain why half of women treated for PD have reoccurring symptoms.
In this study, the investigators propose a couple-based intervention to strengthen couple relationships and support for partners to work together around depression, food insecurity, and PMTCT. Because food insecurity was the most significant problem for women with PD in the formative work, the investigators believe interventions will be most effective if couples can also engage in problem-solving around nutrition, meal preparation, and access to food.
The investigators propose to build on the World Health Organization (WHO) Problem Management Plus (PM+) intervention, which is based on problem-solving therapy (PST) and is effective at reducing depressive symptoms with individuals. PM+ has been adapted for the Malawi context and is currently undergoing an implementation evaluation. The investigators will adapt PM+ for couples with the goal of engaging partners to provide social support for PD, helping women brainstorm and solve problems around PD, food insecurity, and PMTCT adherence, and improving couple communication skills to help couples talk constructively about depression, nutrition and other needs, relationship challenges, and adherence to PMTCT.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Amy Conroy, Ph.D.
- Phone Number: 1 303 522 9439
- Email: amy.conroy@ucsf.edu
Study Contact Backup
- Name: James Mkandawire, MPH
- Phone Number: +265(0) 999412756
- Email: James3mkandawire@gmail.com
Study Locations
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Zomba, Malawi
- Recruiting
- Invest in Knowledge (IKI)
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Contact:
- James Mkandawire, MPH
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Contact:
- Nancy Mulauzi
- Phone Number: 265 (0) 888370081
- Email: nancy.mulauzi@gmail.com
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- In a marriage or cohabitating union for at least 6 months.
- One member of the couple is a woman in the second or third trimester of pregnancy who is living with HIV and screens positive for depression (>10 on the PHQ9).
- Have revealed their HIV status to their partner if living with HIV>
Exclusion Criteria:
- Fear their safety would be at risk.
- Report incidents of severe intimate partner violence (IPV) in the past three months using the WHO IPV measure.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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No Intervention: Enhanced Usual Care
Standard of care, e.g., regular HIV care, regular perinatal care, referrals to services for depression
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Experimental: Couple-based problem solving
A couples-based intervention to support perinatal women who are experience symptoms of depression.
We will adapt the WHO Problem Management Plus manual for this study.
There are 5 sessions that deal with stress management, problem-solving, behavioral activation, and skills to strengthen social support.
The final session will be modified to enhance couple communication skills.
Because many of our participants will be dealing with food scarcity, we will develop a priori strategies to help couple brainstorm dealing with this issue.
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A couples-based problem solving program to deal with depression, PMTCT adherence, and couple communication.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Acceptability
Time Frame: Assessed at the 3-month post-partum follow-up
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Proportion of couples who report satisfaction with the intervention and proportion who would recommend the intervention to friends and neighbors
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Assessed at the 3-month post-partum follow-up
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Participation in the intervention
Time Frame: following the intervention period, an average of 5 months
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Proportion of couples who attend 75% and 100% of sessions.
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following the intervention period, an average of 5 months
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Retention
Time Frame: through study completion, an average of 11 months
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Proportion of couples who complete the study follow-up surveys at 3 months post-partum and 6 months post-partum
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through study completion, an average of 11 months
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Intervention fidelity
Time Frame: following the intervention period, an average of 5 months
|
Study managers will listen to audio recordings of the intervention sessions and complete checklists to assess whether or not each session component was completed.
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following the intervention period, an average of 5 months
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Adherence to infant prophylaxis
Time Frame: 3 months post-partum
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This is a component of PMTCT.
Women will be asked if they ingested Nevirapine (NVP) during labor and delivery (yes or no).
Using the Visual Analog Scale (VAS), women will estimate adherence to NVP prophylaxis for the infant postpartum.
Higher scores indicated better adherence.
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3 months post-partum
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Infant HIV testing
Time Frame: 3 months post-partum
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This is a component of PMTCT.
Women will self-report whether they tested their infant for HIV after 8 weeks and the result of test (to be confirmed with medical records).
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3 months post-partum
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Breast feeding
Time Frame: 3 months post-partum
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This is a component of adherence to PMTCT.
Women will be asked, "Are you currently exclusively breastfeeding your baby?"
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3 months post-partum
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Breast feeding
Time Frame: 6 months post-partum.
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This is a component of adherence to PMTCT.
Women will be asked, "Are you currently exclusively breastfeeding your baby?"
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6 months post-partum.
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Perinatal depression
Time Frame: 3 months post partum
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Using the Center for Epidemiologic Studies Depression Scale (CES-D scale), which is validated for people living with HIV in SSA.
Scores range from 0 to 60 with higher scores indicating more depression symptomatology.
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3 months post partum
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Perinatal depression
Time Frame: 6 months post-partum
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Using the Center for Epidemiologic Studies Depression Scale (CES-D scale), which is validated for people living with HIV in SSA.
Scores range from 0 to 60 with higher scores indicating more depression symptomatology.
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6 months post-partum
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Perinatal viral suppression
Time Frame: 6 months post-partum
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This is a component of PMTCT.
The lab at Zomba Central Hospital will use plasma samples to measure viral load.
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6 months post-partum
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Perinatal adherence to ART
Time Frame: 3 months post-partum
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This is a component of PMTCT.
Using the Visual Analog Scale (VAS), women will report the proportion of prescribed ART doses taken during pregnancy and postpartum.
Adherence will be defined as taking 100% of the prescribed medication during each time period.
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3 months post-partum
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Perinatal adherence to ART
Time Frame: 6 months post-partum
|
This is a component of PMTCT.
Using the Visual Analog Scale (VAS), women will report the proportion of prescribed ART doses taken during pregnancy and postpartum.
Adherence will be defined as taking 100% of the prescribed medication during each time period.
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6 months post-partum
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Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Amy Conroy, Ph.D., University of California, San Francisco
Publications and helpful links
General Publications
- Bengtson AM, Filipowicz TR, Mphonda S, Udedi M, Kulisewa K, Meltzer-Brody S, Gaynes BN, Go VF, Chibanda D, Verhey R, Hosseinipour MC, Pence BW. An Intervention to Improve Mental Health and HIV Care Engagement Among Perinatal Women in Malawi: A Pilot Randomized Controlled Trial. AIDS Behav. 2023 Nov;27(11):3559-3570. doi: 10.1007/s10461-023-04070-8. Epub 2023 Apr 21.
- Ramchandani P, Stein A, Evans J, O'Connor TG; ALSPAC study team. Paternal depression in the postnatal period and child development: a prospective population study. Lancet. 2005 Jun 25-Jul 1;365(9478):2201-5. doi: 10.1016/S0140-6736(05)66778-5.
- Tuthill EL, Neilands TB, Johnson MO, Sauceda J, Mkandawire J, Conroy AA. A Dyadic Investigation of Relationship Dynamics and Depressive Symptoms in HIV-Affected Couples in Malawi. AIDS Behav. 2019 Dec;23(12):3435-3443. doi: 10.1007/s10461-019-02583-9.
- Coleman SF, Mukasakindi H, Rose AL, Galea JT, Nyirandagijimana B, Hakizimana J, Bienvenue R, Kundu P, Uwimana E, Uwamwezi A, Contreras C, Rodriguez-Cuevas FG, Maza J, Ruderman T, Connolly E, Chalamanda M, Kayira W, Kazoole K, Kelly KK, Wilson JH, Houde AA, Magill EB, Raviola GJ, Smith SL. Adapting Problem Management Plus for Implementation: Lessons Learned from Public Sector Settings Across Rwanda, Peru, Mexico and Malawi. Intervention (Amstelveen). 2021 Jan-Jun;19(1):58-66. Epub 2021 Mar 31.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 23-40685
- R34MH134725 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
The dataset will include self-reported demographic and behavioral data from surveys and laboratory data from blood specimens. Individual-participant level or IPD data will be shared. The data will be made in a de-identified format. In addition to the IPD dataset, the researcher will share the data dictionary and final protocol with amendments.
Identifiable data will be de-identified prior to repository submission. All participant-level data will be preserved and shared through deposition in the NIMH Data Archive (NDA), a controlled access public repository.
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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