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The Effectiveness of a Counselling Intervention on the Uptake of HIV Care Services Among HIV Infected Patients in Uganda

The Effectiveness of a Counselling Intervention on the Uptake of HIV Care Services Among HIV Infected Patients in Uganda

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02497456
Enrollment
338
Registered
2015-07-14
Start date
2015-03-31
Completion date
2016-03-31
Last updated
2016-03-23

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

Conditions

HIV

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

BEHAVIORALFollow-up counselling

Sponsors

London School of Hygiene and Tropical Medicine
CollaboratorOTHER
MRC/UVRI and LSHTM Uganda Research Unit
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Masking
NONE

Eligibility

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

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

MeasureTime 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

MeasureTime frame
Time between blood draw for CD4 cell count testing and attending clinic to receive the results among participants that link to pre-ART care6 months
The time between learning that a participant is eligible for ART and ART initiation6 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

MeasureTime frame
The proportion of individuals who undergo repeat HIV testing within 6 months of testing HIV negative through HBHCT.6 months

Countries

Uganda

Outcome results

None listed

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