HIV
Conditions
Keywords
HIV, Counselling, Care, antiretroviral therapy, linkage, Uganda, Africa
Brief summary
The purpose of this study is to evaluate the impact of follow-up counselling after HIV diagnosis through home-based HIV counselling and testing (HBHCT), on linkage to pre-antiretroviral therapy (pre-ART) care in Uganda.
Detailed description
Data on linkage to pre-antiretroviral therapy (pre-ART) care after HIV diagnosis through home-based HIV counselling and testing (HBHCT) in sub-Saharan Africa (SSA) are scarce. The few existing data suggest that only 13% to 54% of HIV-infected persons identified through HBHCT enter pre-ART care. No studies have rigorously evaluated interventions aimed at improving linkage to pre-ART care following HBHCT in SSA. This study will evaluate the effect of follow-up counselling after HIV diagnosis through HBHCT on linkage to pre-ART care in Masaka, south-western Uganda. The study is a cluster randomised trial of the effectiveness of referral to pre-ART care and follow-up counselling (intervention) compared to referral to pre-ART care only (control), for individuals diagnosed with HIV through HBHCT. The intervention will be administered at months 1 and 2, and linkage to care assessed at month 6 post-HBHCT. Data will be collected on socio-demographic characteristics, sexual risk profile, HIV testing history, HIV status disclosure, linkage to care, CD4 count testing and results, cotrimoxazole prophylaxis, and ART initiation. At least 224 HIV-infected participants will be enrolled from 28 clusters (14/study arm). Approximately 84 HIV-uninfected individuals will also be recruited into the study to reduce the possibility of revealing the sero-status of the HIV-infected participants.
Interventions
Sponsors
Study design
Eligibility
Inclusion criteria
HIV-infected participants Inclusion Criteria: 1. HIV-infected adult (≥18 years) 2. Willing to provide informed consent 3. Willing to receive follow-up counselling at home
Exclusion criteria
1. Previous or current receipt of HIV care from an ART provider 2. On-going participation in other health-related research 3. Intending to change residence in the next 6 months 4. Conditions that may make it difficult to provide informed consent e.g. reported (by the individual, relatives or other community members) on-going psychiatric illness HIV-uninfected participants Inclusion criteria: 1. HIV negative adult (≥18 years) 2. Willing to provide informed consent 3. Willing to receive follow-up counselling at home
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The proportion of HIV-infected participants that register with an anti-retroviral therapy (ART) care provider within 3 and 6 months of HIV diagnosis and referral. | 6 months |
| The time between HIV diagnosis and linkage to pre-ART care. | 6 months |
Secondary
| Measure | Time frame |
|---|---|
| Time between blood draw for CD4 cell count testing and attending clinic to receive the results among participants that link to pre-ART care | 6 months |
| The time between learning that a participant is eligible for ART and ART initiation | 6 months |
| The proportion of participants who report adherence to daily cotrimoxazole prophylaxis at 3 and 6 months after HIV diagnosis through HBHCT among those that link to pre-ART care. | 6 months |
Other
| Measure | Time frame |
|---|---|
| The proportion of individuals who undergo repeat HIV testing within 6 months of testing HIV negative through HBHCT. | 6 months |
Countries
Uganda