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Outcomes of Differentiated Models of Service Delivery for HIV Treatment at Sentinel Sites in South Africa

Not Applicable
Recruiting
Conditions
HIV/AIDS
Registration Number
PACTR202306693114717
Lead Sponsor
Bill and Melinda Gates Foundation
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
15520
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

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.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
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 Outcome Measures
NameTimeMethod
Provider and patient satisfaction
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