A global measure of perceived stress.
S Cohen, T Kamarck, R Mermelstein
https://pubmed.ncbi.nlm.nih.gov/6668417Actively Recruiting
Led by University of Pennsylvania · Updated on 2026-03-13
100
Participants Needed
3
Research Sites
N/A
Total Duration
U
University of Pennsylvania
Lead Sponsor
U
University of Botswana
Collaborating Sponsor
Researchers are evaluating an unconditional cash transfer intervention to improve mental capacity, antiretroviral therapy (ART) adherence, and postpartum retention among pregnant women with HIV in Botswana. This pilot Hybrid Type 2 effectiveness-implementation trial aims to answer whether monthly cash transfers improve mental bandwidth and ART adherence during pregnancy and postpartum compared to usual care. It also assesses the feasibility and acceptability of delivering cash transfers via mobile money in public antenatal clinics and explores barriers and facilitators to implementation. The study enrolls 100 pregnant women with HIV in their second trimester, randomly assigned to two groups: one receives usual care plus 1,000 Botswana Pula (BWP) monthly cash transfers through six months postpartum, and the other receives usual care with standard social support. Participants attend visits at baseline, late pregnancy prior to delivery, and three to six months postpartum. Selected participants will also take part in qualitative interviews to explore their experiences with the intervention. Throughout the study, participants complete surveys, mental bandwidth assessments using the Psychomotor Vigilance Task and Raven's Progressive Matrices, and clinical data are collected from electronic health records. The study measures ART adherence, mental bandwidth, feasibility, and acceptability of the cash transfer intervention at specified visits. Secondary outcomes include food security, stress, psychological distress, pregnancy status, birth outcomes, and clinic attendance. Findings will guide future larger trials and policy development.
CONDITIONS
Cash Transfers to Pregnant Women With HIV
You may qualify if you...
You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - From second trimester through 6 months post-partum
Participants receive usual antenatal care with or without unconditional cash transfers of 1,000 BWP per month from the second trimester through 6 months post-partum.
3 visits (baseline, late pregnancy prior to delivery, and 3-6 months post-partum)
Total: 3 locations
1
Lesirane Clinc
Gaborone, Botswana
Not Yet Recruiting
2
Mafitlhakgosi Clinic
Gaborone, Botswana
Not Yet Recruiting
3
Old Naledi Clinic
Gaborone, Botswana
Actively Recruiting
A
Aaron G Richterman, MD, MPH
C
Charlotte N Babbin, BA
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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S Cohen, T Kamarck, R Mermelstein
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