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Published on: September 6, 2019
Understanding the psychosocial needs of HIV-infected children and families: a qualitative study
Warunee Punpanich1, Roger Detels, Pamina M Gorbach
1Queen Sirikit National Institute of Child Health, College of Medicine, Rangsit University, Bangkok 10400, Thailand.
Insights
Children and caregivers living with HIV/AIDS shared concerns about disclosure, adherence, and discrimination. Addressing these psychosocial needs can improve healthcare services and support for affected families.
Area of Science:
- Pediatric Psychology
- Public Health
- Social Work
Background:
- Children living with HIV/AIDS (PLWH) and their caregivers face unique psychosocial challenges.
- Understanding these challenges is crucial for effective healthcare and support systems.
Purpose of the Study:
- To qualitatively assess the psychosocial needs of children living with HIV/AIDS and their caregivers.
- To identify specific concerns related to the disease and treatment process.
Main Methods:
- Individual in-depth interviews were conducted.
- A semi-structured interview guide was utilized to explore experiences.
Main Results:
- Common concerns included impact on loved ones, disclosure, adherence, behavioral issues, discrimination, and financial constraints.
- Emerging themes specific to this population: unwarranted illness concerns, family communication, guardianship planning, treatment continuity, and confidentiality challenges.
Conclusions:
- Study findings provide a framework for enhancing services, including private sessions, disclosure interventions, and life skills building.
- Recommendations aim to facilitate holistic and humanized healthcare for children living with HIV/AIDS.
Objective:
This study aims to engage children living with HIV/AIDS and their caregivers in a qualitative assessment to address psychosocial needs pertaining to this population. The purpose is to identify unique situations and concerns they experienced in dealing with the disease and ongoing treatment process.
Material And Method:
Individual in-depth interviews using a semi-structured interview guide were employed.
Results:
Thirty-four children (12 boys and 22 girls) aged 8-16 and thirty-five primary caretakers (6 males and 29 females) aged 21-66 participated in this study. Results identified some of the common concerns and challenges shared among this population, including impact of the illness on loved ones, disclosure, adherence, behavioural problems, discrimination, treatment affordability, and financial constraints. Certain issues that emerged as important themes specific to this population include unwarranted concerns about certain aspects of the illness, misinterpretation of the nonverbal clues within families, future child guardianship and placement planning, treatment availability during transitional period, and the challenge of maintaining the confidentiality of the diagnosis.
Conclusion:
The needs and suggestions of the target groups provided the framework for improving the current services such as the provision of private sessions with children separated from their caregivers (especially for older children and adolescents), disclosure intervention, behavioral screening, life skills building, and empowerment mobilization. Thus, the information gained can be used to facilitate the holistic and humanized health care provision for children living with HIV/AIDS.
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