HIV, Trauma Exposure
Conditions
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
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.
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
Study design
Eligibility
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
| Measure | Time frame | Description |
|---|---|---|
| Number of Participants With Viral Suppression at the 12-month Assessment | Up to 12 months | HIV-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
| Measure | Time frame | Description |
|---|---|---|
| HIV Care Engagement - Number of Participants With Missed Visits | up to 12 Months | The 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 Adherence | Up to 12 months | Visit adherence defined as the number of scheduled visits attended. |
| HIV Care Engagement- Number of Participants With Gaps in Care | Up to 12 months | Gaps 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 Constancy | Up to 12 months | Visit 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 Spots | At 12 months | Dried blood spots measuring levels of tenofovir-diphosphate, dichotomized as adherent or non-adherent based on a cutoff of 400 fmol/punch. |
| ART Adherence - Pharmacy Visits | Up to 12 months | ART adherence as defined by the number of pharmacy visits. Determined through medical record abstraction. |
| ART Adherence - Total Number of Pills Dispensed | Up to 12 months | ART adherence as defined by pharmacy refill data, total number of pills dispensed. Determined through medical record abstraction. |
Countries
South Africa
Contacts
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, Continuous | 32.9 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 type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | 1 / 173 | 2 / 172 |
| other Total, other adverse events | 0 / 173 | 0 / 172 |
| serious Total, serious adverse events | 21 / 173 | 7 / 172 |