Paediatric HIV Diagnosis Disclosure Clinical Trial
Official title:
Comparative Effectiveness of Pediatric HIV Disclosure Interventions in Uganda
| Verified date | April 2017 |
| Source | University of Connecticut |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
With increased availability of antiretroviral therapy (ART) and improved care, increasing
numbers of perinatally infected children are surviving into adolescence. While HIV care and
treatment programs are expanding, growing challenge faced by health providers and caregivers
is diagnosis disclosure to HIV infected children.
The investigators propose a 4 year project to test the effectiveness of a
cognitive-behavioural intervention that the investigators have designed to support
developmentally appropriate disclosure to HIV infected children by their caregiver.
The investigators hypothesize that the intervention will lead to increased disclosure rates
and will over time improve health and mental health outcomes among caregivers and children
in the intervention group compared to those receiving standard care. The findings of the
study will inform Ugandan and other countries' national policies on pediatric HIV care and
treatment.
| Status | Completed |
| Enrollment | 600 |
| Est. completion date | November 2016 |
| Est. primary completion date | November 2016 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 7 Years and older |
| Eligibility |
Inclusion criteria: - children of age 7 to 12 years; - confirmed HIV-infected; - unaware of their HIV status, according to caregiver report; - principal caregiver, age 18 years or older, of the eligible study child is able and willing to participate in their regular treatment program (monthly visits) and data collection visits at the study clinic at 6-month intervals for 24 months; - agreement to participate in 3 group sessions with other caregivers over a 6 week period, and 3 counseling session with the eligible child(ren), scheduled at the same time as usual clinic visits; - resides within a 30km radius around the study clinic, and not planning on moving during the study period; caregiver and child must both consent / assent for participation. Exclusion criteria: - caregivers and children who are unable to consent or assent to participation in the study due to cognitive impairment or illness; - for children, medical history of serious birth complications, severe malnutrition, bacterial meningitis, encephalitis, cerebral malaria, or other known brain injury or disorder requiring hospitalization or continued evidence of seizure or other neurological disability; - for caregivers, severe mental illness or developmental disability. |
| Country | Name | City | State |
|---|---|---|---|
| Uganda | Kampala City Council Authority (KCCA) Kiswa Health Centre | Kampala | |
| Uganda | KCCA Kawaala Health Centre | Kampala | |
| Uganda | KCCA Kisenyi Health Centre | Kampala | |
| Uganda | KCCA Kitebi Health Centre | Kampala | |
| Uganda | Makerere University-Johns Hopkins University Research Collaboration (MUJHU) clinic | Kampala | |
| Uganda | Nsambya Health Clinic | Kampala |
| Lead Sponsor | Collaborator |
|---|---|
| University of Connecticut | Makerere University-Johns Hopkins University Research Collaboration |
Uganda,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Disclosure to child of child's HIV-positive status | 24 months | ||
| Secondary | HIV related morbidity | For all children and HIV-infected caregivers, information on WHO stage of HIV infection, treatment status, opportunistic infections, CD4 counts will be abstracted from medical records. | 24 months | |
| Secondary | Child antiretroviral medication adherence | 24 months | ||
| Secondary | Cost and Cost-effectiveness | 24 months | ||
| Secondary | Caregiver depression/anxiety | 24 months | ||
| Secondary | Child behavior checklist | captures depression, anxiety and behavior using the child behavior checklist | 24 months |