To be included are those: | |
(i) 18 years of age or older and willing to provide written informed consent, | |
(ii) willing to participate in the MMD model (arm) that the patient’s study cluster has been randomized to | |
(iii) On ART ≥ 6 months with no periods of defaulting on treatment since the last VL result (ART default defined as missing 7 or more consecutive days of ART | |
(iv) On first-line ART regimen (substitutions within the first-line regimen prior to the last VL test are permissible) | |
(v) No ARV drug substitutions since the last VL result < 1,000 copies/ml and plasma or dried-blood spot VL < 1,000 copies/ml in a patient who has been on first-line ART for at least 6 months, with VL drawn within last 12 months of enrolment while patient is receiving ART | |
To be excluded are those: | |
(i) on any other ART line regimen | |
(ii) with co-morbidities requiring more frequent facility visits | |
(iii) ART substitutions since last VL test (iv) diagnosed with a WHO clinical stage 3 or 4 condition within the past 3 months | |
(iv) pregnant or less than 12 months postpartum and breastfeeding mothers | |
(v) participating in another study that involves dispensing interval, adherence, or retention or involves receiving medications |