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The potential participants will be informed of the study details, including the study objectives. Once they have read the study information sheet and have a good understanding of the study, those who intend to participate in the study will be asked to sign the consent form for this study. There are 2 groups of participants: MSM who seek HIV voluntary counseling and testing service (phase I) and MSM who meet nPEP criteria (phase II).
Full description
This study design is mixed-method, starting with quantitative research and followed by qualitative research. The study will be conducted in 2 phases: a cross-sectional study during phase I and a prospective descriptive study during phase II, which will use qualitative research techniques to help understand and define obstacles and uncover opportunities to improve adherence to post-exposure prophylaxis.
During phase I, this study is a quantitative research study using a cross-sectional study design which aims to enroll 450 men who have sex with men (MSM) within 6 months and to collect data by administration of questionnaire amongst all MSM via face-to-face interview. During phase II, we will use a quantitative research design and perform in-depth interviews with those MSM who choose to receive and choose not to receive nPEP despite the fact that they meet nPEP criteria. We expect to identify approximately 50 MSM who meet nPEP criteria during the enrollment period. The number of volunteers will be determined based on saturation theory in which the data collection will be considered complete after analysis of the data shows that additional entries provide no further information (64). The number of volunteers in phase II may not be able to be specified with certainty in advance. Enrollment of subjects will stop once data acquisition is saturated.
An initial review of demographic data and sexual behavior amongst MSM seen at the TRC-ARC will be undertaken by interviewing the TRC-ARC staff who are responsible for looking after this population. This process will aid understanding of clinic logistics and help identify opportunities to meet with MSM individuals. The potential participants will be informed of the study details, including the study objectives. Once they have read the study information sheet and have a good understanding of the study, those who intend to participate in the study will be asked to sign the consent form for this study. There are 2 groups of participants: MSM who seek HIV voluntary counseling and testing service (phase I) and MSM who meet nPEP criteria (phase II).
Phase I. MSM who seek HIV voluntary counseling and testing
Phase II. MSM who receive nPEP
At each of these study visits, the participant will receive risk reduction counseling along with the provision of condoms and lubricant
In accordance to the standard of care at the Anonymous Clinic, TRC-ARC, participants who decide to take nPEP (whose risk of HIV exposure must be within the preceding 72 hours) will receive 3 antiretroviral medications; 2 nucleoside reverse transcriptase inhibitors plus 1 protease inhibitor or non-nucleoside reverse transcriptase inhibitor. The clients will receive HIV antibody testing prior to taking nPEP and at week 6 after starting nPEP.
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Inclusion and exclusion criteria
Phase I
Inclusion criteria:
Exclusion criteria:
Phase II
Inclusion criteria:
Exclusion criteria:
450 participants in 1 patient group
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Data sourced from clinicaltrials.gov
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