HIV/AIDS
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Domain 1 (Provider time) ? Patient-facing or patient-supporting service provider at the study site (patient-supporting providers include data clerks, pharmacists, etc.) ? Directly or indirectly involved in the site’s implementation of ART and DSD models ? Employed in current role at the study site for at least six months ? Provides written informed consent to participate Domain 2 (Provider experiences) ? Direct or indirect service provider at the study site (indirect providers include supervisors, technical advisors, etc.) ? Directly or indirectly involved in the site’s implementation of ART and DSD models ? Employed in current role at the study site for at least six months ? Provides written informed consent to participate. Domain 3 (Patient experiences with service delivery) ? Living with HIV and on ART for at least six months at the study site ? = 18 years old (18 and older considered adult for research purposes in South Africa) ? Enrolled in a specified model of care (including conventional care) up to the target number of participants for that model and have received at least one medication refill under this model ? Provide written informed consent to participate Domain 5 (Patient experience with differentiated HIV testing) ? Undergoing HIV testing at the study site or other testing site within the catchment area ? = 18 years old (18 and older considered adult for research purposes in South Africa) ? Provide written informed consent to participate.
Exclusion criteria
Exclusion criteria: Domain 1 (Provider time) ? None Domain 2 (Provider experiences) ? Direct or indirect service provider at the study site (indirect providers include supervisors, technical advisors, etc.) ? Directly or indirectly involved in the site’s implementation of ART and DSD models ? Employed in current role at the study site for at least six months ? Provides written informed consent to participate. Domain 3 (Patient experiences with service delivery) ? Unable to communicate in any of the languages into which the questionnaire has been translated or that is known to the research assistant ? Not physically, mentally, or emotionally able to participate in the study, in the opinion of the investigators or study staff. ? Unwilling to take the time required to complete the questionnaire on the day of consent. Domain 5 (Patient experience with differentiated HIV testing) ? Unable to communicate in any of the languages into which the questionnaire has been translated or that is known to the research assistant ? Not physically, mentally, or emotionally able to participate in the study, in the opinion of the investigators or study staff. ? Unwilling to take the time required to complete the questionnaire on the day of consent.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Increased clinic efficiency and capacity;Lower costs to providers and patients;Better health outcomes for HIV and non-HIV patients;Improved access and greater satisfaction with healthcare for patients | — |
Secondary
| Measure | Time frame |
|---|---|
| Provider and patient satisfaction | — |
Countries
South Africa
Contacts
Senior Researcher