Gender-Based Violence
Conditions
Keywords
Gender-Based Violence, PrEP (Pre-exposure Prophylaxis), AIDS Prevention, HIV Prevention
Brief summary
This study is nested within the ongoing DREAMS (Determined, Resilient, Empowered, AIDS-free, and Safe) initiative in Siaya County, Kenya. It will test a pilot intervention that will address barriers to pre-exposure prophylaxis (PrEP) uptake and adherence in adolescent girls and young women (AGYW) to reduce their risk to HIV acquisition, with a focus on barriers stemming from male partners and gender-based violence.
Detailed description
This study is designed to assess feasibility, safety, and preliminary effects of a behavioral intervention aimed at increasing pre-exposure prophylaxis (PrEP) uptake and adherence in adolescent girls and young women (AGYW), with a focus on barriers stemming from male partners and gender-based violence, through a pilot cluster randomized-controlled trial (RCT). This study is nested within the ongoing DREAMS (Determined, Resilient, Empowered, AIDS-free, and Safe) initiative in Siaya County, Kenya. Six DREAMS Safe Spaces and their catchment areas will be randomized to receive this community-level intervention or standard of care. Primary outcomes will include feasibility (recruitment, retention) and safety (ongoing or renewed experience of GBV). The investigators will also determine whether the intervention shows promise in increasing PrEP uptake, adherence, and persistence at 6 months. After the intervention, small group discussions, in-depth interviews with male partners, and provider questionnaires will explore acceptability and effects on PrEP decision making and use. Population: AGYW ages 15-24 enrolled in the DREAMS Initiative in Siaya County, Kenya, and, for in-depth interviews only, a subset of male partners of DREAMS participants. Objectives: The goal of this work is to test the feasibility, acceptability, safety, and preliminary effects of the intervention on PrEP uptake and adherence among AGYW. The primary objectives are to assess: 1. Intervention safety 2. Feasibility of delivering the intervention within DREAMS operations 3. Acceptability of the intervention to participants, staff, and male partners. The secondary objectives are to measure the intervention's effect on PrEP uptake, adherence, and persistence at 6 months. Endpoints: The endpoints for the primary objectives are: 1. Self-report of new or ongoing GBV, social harms, serious adverse events, or unanticipated problems during study participation, in the intervention arm versus the comparison arm. 2. Measures of feasibility including recruitment, retention, intervention participation, and fidelity of intervention delivery. 3. Qualitative and quantitative reports of intervention acceptability among participants, quantitative reports of acceptability among providers, and qualitative reports of acceptability among male partners. The endpoints for the secondary objectives are: 1. PrEP uptake: Among participants who are not on PrEP at study enrollment, the proportion of who receive a PrEP prescription during follow-up in the intervention arm vs. the control arm 2. PrEP adherence: Among participants who were dispensed PrEP during the study, the proportion with \>85% adherence over the duration of PrEP use and in the last month of PrEP use, according to Wisepill data in the intervention arm vs. the control arm. 3. PrEP persistence: Among study participants who were dispensed PrEP during the study, the proportion of scheduled PrEP refills that were dispensed, in the intervention arm compared to the control arm.
Interventions
BEHAVIORALTu'Washindi intervention
The intervention includes the following components: 1. PrEP sensitization for men (community level). These activities will aim to provide men with basic information about PrEP and will be used to prepare men for more effective engagement in Buddy Days, described below. 2. Buddy Days (partner level). Buddy days will target male partner engagement by inviting couples to attend a community-wide event with health screenings, and PrEP sensitization, which aim to facilitate further communications about PrEP and increase men's support for AGYW's PrEP use. 3. Adherence support clubs (individual and peer levels). Support clubs will provide a forum for AGYW to discuss challenges and successes around PrEP use in relationships, including in the context of partner violence. Participation in these groups is hypothesized to increase self-efficacy for PrEP use by reducing social isolation and providing additional positive role-modeling from peer leaders.
OTHERControl
Standard of care will include PrEP delivery according to the usual DREAMS procedures, including attendance at routine Safe Space meetings and routine PrEP provision at the Safe Space, if applicable.
Sponsors
Impact Research & Development Organization
National Institute of Mental Health (NIMH)
RTI International
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE
Intervention model description
cluster randomized-controlled trial (RCT)
Eligibility
Sex/Gender
FEMALE
Age
15 Years to 24 Years
Healthy volunteers
Yes
Inclusion criteria
* 1\) Age 15-24 years (inclusive); * 2\) HIV-negative, by self-report; * 3\) At high risk for acquiring HIV, as defined by the 2016 Guidelines on Use of Antiretroviral Drugs for Treating and Preventing HIV Infections in Kenya; * 4\) Fluent in English, Dholuo, or Swahili; * 5\) Enrolled in DREAMS (defined by having a DREAMS identification (ID) number); * 6\) Lives within the Safe Space catchment area - 7) Willing and able to attend support groups over the 6-month period; * 8\) Potentially interested in PrEP and/or using PrEP already; * 9\) Able and willing to provide adequate locator information, as defined in site standard operating procedures (SOPs); * 10)If aged 18 and above: Willing and able to provide informed consent; * 11)If non-mature minor aged 15-17: Willing and able to provide assent and parent or guardian willing and able to provide parental consent; * 12)If mature minor aged 15-17: Willing and able to provide informed consent or to provide assent and parent or guardian consent, per participant choice.
Exclusion criteria
* 1)Planning to relocate away from the study catchment area in the next 6 months; * 2)Planning to travel away from the study catchment area for a time period that would interfere with study participation; or * 3\) Has any condition that, in the opinion of the site PI, would preclude informed assent/consent, make study participation unsafe, complicate interpretation of study outcome data, or otherwise interfere with achieving the study objectives.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Acceptability of the behavioral intervention - qualitative data from male partners | 6 months | Qualitative reports of intervention acceptability among male partners. These will include in-depth interviews covering topics such as satisfaction with content, delivery, and length of the intervention, as well as reported impact on the male partner's life. |
| Acceptability of the behavioral intervention - qualitative data from participants | 6 months | Acceptability measures include qualitative reports of intervention acceptability among participants. These will include in-depth interviews covering topics such as satisfaction with content, delivery, and length of the intervention, as well as reported impact on the participant's life. |
| Acceptability of the behavioral intervention - quantitative data from participants | 6 months | Quantitative reports of intervention acceptability among participants. Satisfaction with intervention content, delivery, length using the client satisfaction questionnaire and as measured on a likert scale response and as open-ended response options. |
| Acceptability of the behavioral intervention - quantitative data from providers | 6 months | Satisfaction with intervention content, delivery, length using the client satisfaction questionnaire and as measured on a likert scale response and as open-ended response options. |
| Intervention safety - survey tool | 3 months | Self-report of experience of social harms in the past 3 months and violence or controlling behavior using an adapted version of the World Health Organization's questions on violence against women. Behaviors are reported for every experience in the past 3 months and frequency of experience (e.g., once, few times, many times). |
| Intervention safety - form | Throughout the study, approximately 6 months | Reports of new or ongoing gender-based violence (GBV), social harms, serious adverse events, or unanticipated problems during study participation. Information will be self-reported using an specially-developed form |
| Feasibility of the behavioral intervention - Process Indicators | Throughout the study, approximately 6 months | Measures of feasibility including recruitment timelines and numbers enrolled, retention rates, intervention participation measured by attendance at support club sessions and other intervention activities, and fidelity of intervention delivery measured through documented observations of intervention delivery capturing activities administered and ratings of quality. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Proportion of participants with Pre-Exposure Prophylaxis (PrEP) adherence > 85% at six months | Throughout the study, approximately 6 months | Among participants who were dispensed PrEP during the study, the proportion with \>85% adherence over the duration of PrEP use and in the last month of PrEP use, according to Wisepill data. This information will be collected using the Wisepill electronic data monitoring (EDM) device that collects information on pill adherence in real-time. |
| Pre-Exposure Prophylaxis (PrEP) persistence among participants at six months | 6 months | Among study participants who were dispensed PrEP during the study, the number of scheduled PrEP refills that were dispensed. This will be measured through retrospective clinic record abstraction reflecting clinic visits throughout the study period. |
| Pre-Exposure Prophylaxis (PrEP) uptake | 6 months | Among participants who are not on PrEP at study enrollment, the number who receive a PrEP prescription during follow-up. This will be measured through retrospective clinic record extraction. |
Countries
Kenya
Outcome results
None listed