Abstract
Objective
We aimed to: (1) follow parents and guardians through the process of paediatric HIV disclosure to understand how often pre-disclosure worries are realised; and (2) estimate the effects of disclosure on child, caregiver, and family well-being.
Design
We conducted a 12-month prospective cohort study in Zimbabwe with 123 primary caregivers of children ages 9 to 15 years who were HIV positive but did not know their serostatus at baseline. By the end of the study period 65 caregivers reported that their child learned his or her HIV-positive status.
Main Outcome Measures
We used three waves of data to compare caregivers’ pre-disclosure worries to post-disclosure reports and to characterise associations between disclosure and well-being of the child (Strengths and Difficulties Questionnaire), caregiver (Patient Health Questionnaire-9), and family (Family Relationship Quality) over time.
Results
Caregivers’ pre-disclosure worries and fears about how their child would react to disclosure of their HIV status largely went unrealised. Furthermore, we did not find strong evidence of clinically-important increases in problems on average following disclosure.
Conclusion
Findings support the call to identify supportive intervention strategies that address caregiver fears at the beginning of the disclosure process.
Disclosure statement
The authors have no conflicts of interest to disclose.
Data availability
Data and code available at https://ericpgreen.github.io/r2d2/.