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A Randomized Trial of ImpACT+, a Coping Intervention for HIV Infected Women With Sexual Trauma in South Africa

Project Someleze: A Randomized Trial of ImpACT+, a Coping Intervention to Improve Clinical and Mental Health Outcomes Among HIV-infected Women With Sexual Trauma in South Africa

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04793217
Acronym
ImpACT+
Enrollment
350
Registered
2021-03-11
Start date
2021-02-18
Completion date
2025-07-03
Last updated
2026-08-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV, Trauma Exposure

Keywords

South Africa, HIV, Mental health, Trauma, Women

Brief summary

ImpACT+ (Improving AIDS Care after Trauma+), is an individual-level coping intervention to address traumatic stress and HIV care engagement among South African women with sexual trauma histories. We propose a full-scale randomized controlled trial to examine the effect of ImpACT+ on clinical outcomes in the period after ART initiation and to understand mental health and behavioral mechanisms through which viral suppression can be achieved. ImpACT+ will target women who are initiating ART in order to take advantage of a window of opportunity in HIV care and maximize care engagement. The aims are to test the effectiveness of ImpACT+ and explore its potential for implementation.

Detailed description

Addressing sexual trauma in the context of HIV care is essential to improve clinical outcomes and mental health among women in South Africa. Women represent nearly two-thirds of the South African HIV epidemic, and they report disproportionately high rates of sexual trauma, which negatively impacts their mental health and may lead to avoidant coping behaviors. The psychological sequaelae of trauma can adversely impact retention in HIV care and adherence to antiretroviral therapy (ART), which may in turn reduce viral suppression and increase the risk of HIV transmission to others. HIV care engagement may be particularly challenging in South Africa, where women face dual epidemics of HIV and sexual violence, with limited access to mental health treatment. In this setting, interventions that address barriers to effective HIV care engagement and improve health outcomes across the care continuum are urgently needed. The primary objective of this study is to evaluate the effectiveness of ImpACT+ (Improving AIDS Care after Trauma+), an individual-level intervention based on theories of stress and coping, on clinical outcomes among HIV-infected women with sexual trauma. Secondary objectives include determining whether reductions in traumatic stress and avoidant coping mediate intervention effects on clinical outcomes, and assessing potential for scalability and full-scale implementation. ImpACT+ was developed and culturally adapted to the South African context, targeting women who are initiating ART (classified clinically as naïve initiators, restarters or defaulters) to make use of a window of opportunity in HIV care and maximize impact on care engagement. The proposed five-year study seeks to rigorously evaluate ImpACT+, using a hybrid effectiveness-implementation design (Hybrid Type I), with three specific aims: (1) evaluate the effectiveness of ImpACT+ on viral suppression, ART adherence, and HIV care engagement; (2) assess the degree to which reductions in PTSD symptoms and avoidant coping mediate intervention effects; and (3) explore potential for scalability and full-scale implementation. The trial will enroll 350 women who have initiated ART and have a history of sexual trauma and elevated traumatic stress. Participants will be randomized to the ImpACT+ intervention condition (six weekly sessions, with six maintenance check-ins over the 12-month follow-up period) or the control condition (three weekly sessions of Problem Solving Therapy (PST)). All participants will complete a baseline assessment at enrollment (within four months of initiating ART), with additional behavioral assessments and viral load testing at 4-month, 8-month, and 12-month follow-up. ART adherence will also be assessed using dried blood spot (DBS) biomarkers, and care engagement data will be extracted from medical records at the end of the study period. This study is one of the first full-scale trials of a trauma-informed intervention on clinical outcomes for HIV-infected women. If effective, ImpACT+ will fill a critical void in evidence-based trauma interventions in this setting and combat the drop-off across the HIV continuum of care in South Africa, as well as inform such approaches in the U.S. and globally.

Interventions

BEHAVIORALImproving AIDS Care After Trauma +

ImpACT+ integrates skills for HIV treatment adherence and coping with trauma, tailored to the South African context. This includes exploration of values informing care engagement, recognizing the synergistic stress of sexual trauma and HIV, understanding the contribution of stressors to maladaptive coping, and developing adaptive methods for coping as alternatives to avoidance. ImpACT+ will be delivered in private spaces at the primary care clinic and will consist of 6 individual sessions followed by 6 maintenance check-ins. Individual sessions focus on coping, adherence, and care engagement during an early critical period, while maintenance check-ins reinforce positive change and support ongoing implementation of skills. Evidence supports a 6-session format in low-resource settings. Individual sessions will begin within 2 weeks after the baseline survey and be completed by the 4-month assessment. Maintenance check-ins will begin following the 4-month assessment.

BEHAVIORALAdapted Problem-Solving Therapy

Participants will receive three weekly individual sessions of adapted PST. The goal of PST is to identify problems that interfere with daily activities and address them through problem-orientation work. We anticipate stressors will include (a) relationship difficulties, including family stress, (b) financial stress and unemployment, (c) general impact of HIV infection, and (d) overall chronic stress. Thus, PST may indirectly address stressors that may impact care engagement, but will not address the intersection of HIV and trauma specifically.

Sponsors

Columbia University
Lead SponsorOTHER
University of Cape Town
CollaboratorOTHER
National Institute of Mental Health (NIMH)
CollaboratorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Women with HIV who receive care at either study clinic * \>2 weeks to \<4 months since ART initiation * History of sexual trauma * Meets criteria for traumatic stress * Xhosa speaking

Exclusion criteria

\- High suicide risk

Design outcomes

Primary

MeasureTime frameDescription
Number of Participants With Viral Suppression at the 12-month AssessmentUp to 12 monthsHIV-1 RNA viral load (COBAS AmpliPrep/COBAS TaqMan HIV-1 Test, v2.0, Roche). Viral suppression defined as \<50 copies/ml. Continuous measures of viral load, modeled using a log10 transformation.

Secondary

MeasureTime frameDescription
HIV Care Engagement - Number of Participants With Missed Visitsup to 12 MonthsThe number of participants with missed visits as determined by medical record review. A missed visit was defined as missing a scheduled visit by more than two weeks from the scheduled date, which aligned with the clinics' definition.
HIV Care Engagement- Visit AdherenceUp to 12 monthsVisit adherence defined as the number of scheduled visits attended.
HIV Care Engagement- Number of Participants With Gaps in CareUp to 12 monthsGaps in care defined as whether \>90 days have elapsed between visits without sufficient numbers of pills given to cover the gap, as determined by medical record abstraction.
HIV Care Engagement- Visit ConstancyUp to 12 monthsVisit constancy defined as the number of 90-day intervals with \>1 completed visit, determined by medical record abstraction.
Number of Participants With ART Adherence - Dried Blood SpotsAt 12 monthsDried blood spots measuring levels of tenofovir-diphosphate, dichotomized as adherent or non-adherent based on a cutoff of 400 fmol/punch.
ART Adherence - Pharmacy VisitsUp to 12 monthsART adherence as defined by the number of pharmacy visits. Determined through medical record abstraction.
ART Adherence - Total Number of Pills DispensedUp to 12 monthsART adherence as defined by pharmacy refill data, total number of pills dispensed. Determined through medical record abstraction.

Countries

South Africa

Contacts

PRINCIPAL_INVESTIGATORKathleen J Sikkema, PhD

Columbia University

Participant flow

Pre-assignment details

350 participants were enrolled. One participant withdrew from the study prior to randomization and thus is not counted here. Randomization occurred at the participant level. No units other than participants were assigned in this study.

Baseline characteristics

Characteristic
Age, Continuous32.9 years
STANDARD_DEVIATION 9.4
Coping
Active Coping
3.3 points
STANDARD_DEVIATION 0.7
Coping
Avoidant Coping
2.7 points
STANDARD_DEVIATION 0.8
Coping
Social/Spiritual Coping
2.3 points
STANDARD_DEVIATION 0.8
PTSD (PCL-5)39.7 score on a scale
STANDARD_DEVIATION 19.2
Race/Ethnicity, Customized
Black African
170 Participants
Race/Ethnicity, Customized
Other - Coloured
4 Participants
Sex: Female, Male
Female
173 Participants
Sex: Female, Male
Male
0 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
1 / 1732 / 172
other
Total, other adverse events
0 / 1730 / 172
serious
Total, serious adverse events
21 / 1737 / 172

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 29, 2026