PrEP Promotion Package
OtherA PrEP promotion package will be developed to test if this will change uptake, acceptance, retention and PrEP knowledge
NCT Number: NCT03254550
This stepped-wedge cluster-randomized trial is embedded in an 18-month observational cohort study that has the aim to assess the operationalization of oral Pre-Exposure Prophylaxis (PrEP) in Swaziland as an additional HIV combination prevention method among individuals at high risk of HIV infection. The trial aims to determine the effect of a healthcare facility-based PrEP promotion package on the number of clients who take up PrEP.
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Notify Me16 year and older
All sexes
Interventional
Not applicable
Hhukwini Clinic, Hhukwini, Hhohho Region, Eswatini
The study will assess who will be reached with an introduction to and an offer of PrEP - and who will take up PrEP - when PrEP becomes available through different delivery points in the public-sector health system, including outpatient department (OPD), antenatal care (ANC), postnatal care (PNC) , family planning (FP) , and following HIV counseling and testing (VCT).
In addition to PrEP reach and PrEP uptake, the study aims to establish PrEP retention and average costs per client, by different health systems delivery points and to assess the effectiveness of a feasible and low-cost PrEP Promotion Package (PPP). The exact composition of PPP will be informed by findings from in-depth- interviews with clients, providers, and PrEP stakeholders. The effect of the PPP on the monthly number of clients who are initiated on PrEP will be studied using a stepped-wedge cluster-randomized design. Specifically, the trial will have two sequences with three healthcare facilities in each sequence, and three periods. In the first period, all healthcare facilities will be in the control phase; in the second period three healthcare facilities will implement the PPP; and in the third period all six healthcare facilities will implement the PPP.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
A PrEP promotion package will be developed to test if this will change uptake, acceptance, retention and PrEP knowledge
Time frame: 18 months
The monthly number of clients who was initiated on PrEP
Time frame: 18 months
The monthly number of clients who underwent a risk assessment for PrEP eligibility
Time frame: 18 months
The monthly number of clients who was identified as being at a substantial risk of acquiring HIV
Time frame: 18 months
% of HIV-negative clients at substantial risk for HIV infection who accepted a PrEP offer
Time frame: 12 months
The monthly number of clients who either took up PrEP or were linked to antiretroviral therapy
Time frame: 6 months
% of clients taking PrEP who were retained at six months after PrEP initiation. Retention was defined as attending all follow-up visits during the first 180 days after PrEP initiation not more than seven days after the scheduled appointment.
Time frame: 18 month
% of clients initiated on PrEP who seroconverted during the first six months after taking up PrEP.
Clinton Health Access Initiative Inc.
Other
Expanding Options for HIV Prevention Through Pre-exposure Prophylaxis in Hhohho Region, Swaziland
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.