Elsevier

The Journal of Pediatrics

Volume 116, Issue 2, February 1990, Pages 207-213
The Journal of Pediatrics

Original article
Children's knowledge of cancer and its treatment: Impact of an oncology camp experience

https://doi.org/10.1016/S0022-3476(05)82876-8Get rights and content

Because pediatric oncology camps provide an opportunity for children who have had cancer to interact with their peers in an informal, recreational environment, this study was designed to determine (1) whether cancer and its treatment are discussed informally among the children, (2) what kinds of information are exchanged if such discussions take place, and (3) how these interaction might affect the children's knowledge and understanding of cancer and its treatment. The study included detailed, open-ended, structured interviews and observational accounts of the subjects before, during, and after camp. These interviews and observations in a sample of 50 children revealed that the children engaged in informal discussion about cancer and its treatment, and that information on a variety of topics, ranging from medical procedures to prognosis, was exchanged. Despite the lack of formal instruction, there was a significant increase in the children's knowledge about cancer and its treatment. Age, sex, diagnosis, years since diagnosis, treatment status and times at camp were not found to be significant determinants of gain in knowledge. No control group was studied, but we believe that the data support the conclusion that attending a camp for children with cancer improves their knowledge of the disease and its treatment.

References (12)

  • JamisonRN et al.

    Psychological impact of cancer on adolescents: self-image, locus of control, perception of illness and knowledge of cancer

    J Chronic Dis

    (1986)
  • HvizdalaE et al.

    A summer camp for children with cancer

    Med Pediatr Oncol

    (1978)
  • BensonPJ

    The relationship between self-concept and a summer camping program for children and adolescents who have cancer

    J Assoc Pediatr Oncol Nurs

    (1987)
  • SmithKE et al.

    Impact of a summer camp experience on daily activity and family interactions among children with cancer

    J Pediatr Psychol

    (1987)
  • GreenwoodR et al.

    A very special camp

    Am J Nurs

    (1982)
  • CookTD et al.

    Quasi-experimentation: design and analysis issues for field settings

    (1979)
There are more references available in the full text version of this article.

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