ENhance Initiation and Retention in Isoniazid Preventive Therapy (IPT) Care for HIV Study (ENRICH Study)

The study intervention, combination intervention package (CIP), will contain programmatic, structural and psychosocial components including: 1) health care provider training and mentorship in IPT provision using a clinical algorithm; 2) identification of HIV-infected family members eligible for IPT using a family care enrollment form; 3) review of monitoring data on IPT initiation and adherence during monthly multidisciplinary team meetings; 4) reimbursement of transportation costs to patients for monthly clinic visits; and 5) real-time adherence support using interactive voice response (IVR) via mobile phones and trained peer educators.

Data will be collected from all HIV-infected patients enrolled in HIV care at study sites on or after January 1, 2013; from a subset of patients who initiate IPT and enroll into a measurement cohort (MC); and from program characteristics surveys conducted at the study sites. Routine clinic data from all HIV-infected patients enrolled in HIV care at the 10 participating clinics on or after January 1, 2013 will be used to measure the following outcomes: IPT initiation, completion of IPT, and retention in HIV care. These data will be collected by Research Assistants (RA) by abstracting the following information from the clinic Pre-ART, ART (antiretroviral therapy) and IPT registers during the period of observation on all HIV patients who enrolled in care at a study site on or after January 1, 2013: date of enrollment in HIV care; IPT initiation (yes/no); date of ART initiation (if applicable); IPT outcomes (completion, default, death, stopped, transferred out); TB (tuberculosis) screening results; TB treatment (yes/no); TB treatment outcomes (if applicable); and retention in HIV care.

A measurement cohort of 500 HIV-infected patients initiating IPT on or after July 1, 2013 will be recruited from the 10 clinics (n=250 per study arm). MC participants will be assessed at baseline (enrollment) and monthly intervals for six to nine months, depending on the duration of IPT. Outcomes to be measured among MC participants include: adherence to IPT; adherence to ART (if applicable); change in CD4+ count; and side effects/adverse events. MC participants at both SOC and CIP sites will receive the same assessments. RAs will administer assessments on the day of regularly scheduled clinic visits, including a Baseline interview administered on the day of enrollment (which coincides with the day the participant initiates IPT), monthly follow-up interviews completed throughout IPT, and an end of treatment interview that is completed on the day the participant ends IPT. Participants who miss a study visit will be contacted by study staff and administered the questionnaire over the phone within a 1-week window period of the scheduled clinic visit. RAs will also call the MC participants between clinic visits to conduct unannounced pill counts to assess medication adherence. In addition, 30 MC participants from CIP sites will participate in a qualitative interview to assess feasibility and acceptability of the Interactive Voice Response (IVR) system, one of the interventions in place at CIP sites. Also, three groups will be recruited from CIP clinics to participate in in-depth interviews: IPT initiators, from among participants in the Measurement Cohort (n =15), IPT non-initiators (n=15), and healthcare providers (nurses and peer educators, n=13). In-depth interviews will assess acceptability and preferences of intervention components as well as reasons for IPT non-initiation.

RAs will conduct an assessment of programmatic activities at each HIV clinic prior to study implementation and on a monthly basis thereafter throughout the study period. Clinics in both conditions will receive the same assessments. The RA will administer a brief semi-structured Program Characteristics survey to the ART nurse, who will be most familiar with the day-to-day operations of the HIV clinic. The survey will assess nurse training and mentorship in IPT initiation and HIV treatment; availability and use of an IPT clinical algorithm, IPT and ART adherence training for peer educators (PEs); IPT health education for patients; availability and use of an IPT treatment literacy curriculum, including a flip chart used by PEs; reimbursement for transportation costs for patients; provision of mobile phones, subscriber identification module (SIM) cards and airtime vouchers for HIV patients on IPT; use of IVR messages for medication and appointment reminders and assessment of medication adherence and side effects; and provision of community-based adherence and side effect monitoring by PEs. These data will be used to assess fidelity with the intervention at CIP sites, as well as to measure any potential contamination at SOC sites.

All clinical care will be performed by the clinic staff (nurses and PEs). All study procedures, including participant interviews, pill counts, medical record abstraction, and program characteristics surveys will be performed by study staff (research assistants). Following routine clinic visits, clinic staff will refer patients initiating IPT to study staff, who will screen for eligibility, obtain informed consent, and enroll consenting eligible patients into the MC. In addition, RAs at CIP sites will provide parts of the intervention, including disbursement of mobile phones, SIM cards, airtime vouchers, and cash for transportation reimbursement to eligible patients.