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Syndemics and Loss from the HIV Care Continuum in India - Intervention

Syndemics and Loss from the HIV Care Continuum in India - Intervention

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03966586
Enrollment
50
Registered
2019-05-29
Start date
2019-06-20
Completion date
2023-12-01
Last updated
2025-02-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV Infections

Keywords

hiv, India, retention, continuum

Brief summary

The investigators will assess the feasibility and acceptability of a pilot intervention to keep people living with HIV (PLHIV) in southern India in care and virologically suppressed. The lack of understanding of the causes of loss from the HIV care continuum in India stifles the armamentarium of effective interventions to keep Indian PLHIV in care. The results of this research will demonstrate the feasibility and acceptability of a pilot intervention targeting the multiple mechanisms by which PLHIV become lost to care. By targeting these mechanisms, this intervention will be designed to be scalable in a setting where access to mental health specialists is limited.

Detailed description

This pilot intervention represents the final Aim of the NIMH-sponsored study Syndemics and Loss from the HIV Care Continuum in India. This trial will be conducted at the Y.R. Gaitonde Centre for AIDS Research and Education (YRG CARE), located in Chennai, the capital of Tamil Nadu state and one of the epicenters of the Indian HIV epidemic. The investigators will recruit 50 adult (age \>=18) PLHIV presenting to care at YRG CARE and ART-naïve. Participants will be recruited at their first visit to YRG CARE, at which the participant's HIV diagnosis is established or confirmed and the participant receives initial counseling and clinical care. At this recruitment stage, research assistants will conduct a pre-intervention questionnaire including measures of depressive symptoms, internalized stigma, self-efficacy, mental health, and physical health. The investigators will then randomize the patient to usual care vs. enhanced-care intervention (25 in each arm). The enhanced-care intervention will be multi-faceted, reflecting the likelihood of multiple syndemic conditions as well as evidence from LMICs suggesting that programs combining multiple approaches are the most effective in improving retention in care. The enhanced-care intervention will consist of the following components: 1. Active outreach, including bidirectional weekly SMS messaging / automated voice messaging (depending on literacy) 2. Appointments (specific appointment times/dates). 3. Financial support, including free clinic visits, labs, medications, and transportation incentives on a sliding scale based on distance to clinic 4. Microenterprise, including bag-making or food-making ventures for women 5. Enhanced counseling. Participants in the enhanced-care intervention will participate in an individual enhanced counseling program called Steps to Success, based upon a Life Steps and Problem Solving curriculum.

Interventions

BEHAVIORALActive outreach

Participants will get bidirectional weekly SMS messaging / automated voice messaging (depending on literacy), with messages to be programmed by the participant in the enhanced counseling sessions.

BEHAVIORALAppointments

Participants in the enhanced-care intervention will be given specific appointment times/dates.

Participants in the enhanced-care intervention will receive free clinic visits, labs, and medications. They will also receive transportation incentives on a sliding scale based on distance to clinic, to range between 200-700 INR to be given each clinic/study visit. All participants, in both the usual care and enhanced care arms, will be offered VL testing free of charge, although this will not be known to the participants prior to the visit.

BEHAVIORALMicroenterprise

YRG CARE is affiliated with two microenterprise programs in bag-making and food-vending which can be leveraged as part of an intervention, particularly for women. There is an established training and mentoring program for individuals who wish to join the bag-making or food-making ventures. Participants who opt for this will be linked to the bag-making and food-vending programs, with all up-front costs (e.g. vending kiosk, training, serving materials, etc.) covered.

Participants in the enhanced-care intervention will participant in an individual enhanced counseling program called Steps to Success, based upon a Life Steps and Problem Solving curriculum. Steps to Success will consist of five one-on-one sessions of approximately 1 to 1.5 hours each. The first session will take place at the time of the participant's second clinical visit to YRG CARE, which will be between 1-3 weeks after the participant is recruited.

BEHAVIORALUsual clinical care and counseling

Usual clinical care and counseling

Sponsors

YR Gaitonde Centre for AIDS Research and Education
CollaboratorOTHER
Brigham and Women's Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult PLHIV presenting to care at YRG CARE who are ART-naïve and who plan to follow-up at YRG CARE * Speaks Tamil, Telugu, or English

Exclusion criteria

* Previous ART exposure * Not competent to provide informed consent or participate in the study

Design outcomes

Primary

MeasureTime frameDescription
Feasibility as assessed by semi-structured qualitative interviews12 monthsMinimal negative impact on clinical work flow and ability to deliver all intervention components, particularly all sessions of enhanced counseling, as measured by semi-structured qualitative interviews of providers
Acceptability among participants and providers as assessed by semi-structured qualitative interviews12 monthsAcceptability among patients and providers as measured by semi-structured qualitative interviews of participants and providers

Secondary

MeasureTime frameDescription
ART initiation success (accepted ART and continued ART for at least 6 months)6 monthsSuccessful ART initiation (accepted ART and continued ART for at least 6 months)
Depressive symptoms as measured by PHQ-912 monthsScore of \>10 indicates probable depression
Internalized stigma as measured by Internalized AIDS-Related Stigma Scale12 monthsIncludes six items related to concerns about disclosure as well as items related to feelings of shame and/or self-hatred. Responses are elicited on a binary scale (yes/no) and scores represent the sum of endorsed items.
Retention in care12 monthsNo unexpected absences \> 90 days
Social support as measured by Multidimensional Scale of Perceived Social Support12 months12 item scale of social support
Food insecurity as measured by Household Food Insecurity Access Scale12 months8 item scale of food insecurity
Self-efficacy as measured by General Self-Efficacy Scale--shortened version12 monthsSix item scale of self-efficacy
Viral suppression (Undetectable HIV-1 RNA, <50 copies / mL)3 monthsUndetectable HIV-1 RNA, \<50 copies / mL

Countries

India

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026