https://doi.org/10.31648/cetl.2061
This paper aims at presenting the results of research carried out during the “Sun and Adventure”
project dedicated for children – cancer survivors. The research focused on sociotherapeutic and
psychosocial benefits for the Project’s participants. The methods involved questionnaire technique:
a slightly modified Polish adaptation of QOLCE (Health-Related Quality of Life in Childhood
Epilepsy) and the Polish adaptation of Spielberger’s state-trait anxiety questionnaire in the version
dedicated to children STAI – C. The results were complemented by interviews carried out with the
participants during the camp organized within the Project framework. Participation in the Project
influenced the quality of life of the cancer survivors, although to a lesser extent than it might have
been expected. The obtained results are relatively minor due to the high initial quality of life level
of the participants. Nevertheless, participation in this program may contribute to positive changes
in the functioning of cancer survivors.
In the view of future editions of the Project, it is necessary to implement more precise
inclusion criteria to maximize the effects of potential positive changes. It appears that such criteria
as good health condition and desire to participate in the Project are insufficient to optimally
select the participants. Inviting children to participate in the “Sun and Adventure” Project (and
similar initiatives aiming at improving quality of life) should be also based on evaluation of the
family environment and the financial situation of the participant, as well as the psychological
consequences of cancer treatment (for example, anxiety, depression, difficulties with group
adaptation). Implications for cancer survivors are following: organized and structured camps
involving physical activity and psychological assistance are profitable for young cancer survivors
whose social development has been affected by their illness and treatment.
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