Parent Perceptions of a Pretend Play Intervention for Their Children With Cancer
- PMID: 36315121
- DOI: 10.1097/jnr.0000000000000532
Parent Perceptions of a Pretend Play Intervention for Their Children With Cancer
Abstract
Background: Although the rate of survival in childhood cancer today is close to 85%, a cancer diagnosis can still turn the world upside down for both children and parents. Often, children in oncology care are frustrated about their inability to control events and activities around them. Therapeutic pretend play has been suggested as a means to encourage children to express and handle emotions in a safe environment.
Purpose: This study was developed to describe and explore parents' experiences of a pretend play intervention that consisted of six to eight play sessions with a play facilitator administered to their children undergoing cancer treatment.
Methods: A descriptive qualitative method was used, including individual interviews with 15 parents.
Results: Three main categories were developed, including (a) experiences of joining the project, (b) perceptions of the play intervention, and (c) reflections on effects and implications, with subcategories evolved for each category. The parents experienced that the play sessions helped improve their children's communication skills and made them more capable of participating in their care. They appreciated that the intervention focused on the child's well-being and saw it as a positive break in their child's cancer treatment. It also helped them better reflect on their own situation.
Conclusions/implications for practice: According to the parents' experiences, pretend play can be a helpful tool for improving children's participation in their cancer care that strengthens their autonomy, emotional repertoire, and communication skills. However, the results also highlighted that some of the children did not fully understand the information provided about this study, which weakened the validity of their consent to participate. Thus, more work is needed on developing age-appropriate information to obtain participation consent from children. In addition, more knowledge is needed regarding how to appropriately include children with cancer in research in an ethically acceptable way.
Copyright © 2023 The Authors. Published by Wolters Kluwer Health, Inc.
Conflict of interest statement
The authors declare no conflicts of interest.
References
-
- Butler A. E., Hall H., Copnell B. (2018). Bereaved parents' experiences of research participation. BMC Palliat Care , 17(1), Article No. 122. https://doi.org/10.1186/s12904-018-0375-4 - DOI
-
- Cousino M. K., Zyzanski S. J., Yamokoski A. D., Hazen R. A., Baker J. N., Noll R. B., Rheingold S. R., Geyer J. R., Alexander S. C., Drotar D., Kodish E. D. (2012). Communicating and understanding the purpose of pediatric phase I cancer trials. Journal of Clinical Oncology , 30(35), 4367–4372. https://10.1200/JCO.2012.42.3004 - DOI
-
- Coyne I., Amory A., Kiernan G., Gibson F. (2014). Children's participation in shared decision-making: Children, adolescents, parents and healthcare professionals' perspectives and experiences. European Journal of Oncology Nursing , 18(3), 273–280. https://doi.org/10.1016/j.ejon.2014.01.006 - DOI
-
- Coyne I., Gallagher P. (2011). Participation in communication and decision-making: Children and young people's experiences in a hospital setting. Journal of Clinical Nursing , 20, 2334–2343. https://doi.org/10.1111/j.1365-2702.2010.03582.x - DOI
-
- Coyne I., Harder M. (2011). Children's participation in decision-making: Balancing protection with shared decision-making using a situational perspective. Journal of Child Health Care , 15(4), 312–319. https://doi.org/10.1177/1367493511406570 - DOI
MeSH terms
LinkOut - more resources
Full Text Sources
Medical
