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Pouy S, Taheri-Ezbarami Z, Rassouli M, Darbandi B, Maroufizadeh S, Javadi-Pashaki N. Investigating the Quality of Palliative Care in Children with Cancer from Parents’ Perspective: A Descriptive Cross-sectional Study in Northern Iran. JGUMS 2025; 34 (2) :158-169
URL: http://journal.gums.ac.ir/article-1-2701-en.html

Background Providing high-quality palliative care, as one of the basic rights of children with cancer, leads to the improvement of the quality of life and satisfaction of the child and family. It is important to evaluate the quality of care to take corrective actions. Hence, the present study was conducted to determine the quality of palliative care for children with cancer in northern Iran.
Objective The present study aimed to determine the quality of palliative care for children with cancer in northern Iran.
Methods This descriptive cross-sectional study was conducted on 200 parents of children with cancer who were referred to the 17-Shahrivar Educational and Remedial Center in Rasht City, Iran, in 2023. The samples were selected by convenience sampling methods according to the inclusion criteria. The inclusion criteria were parents who had a child with cancer, were interested in participating in the study, and could read. Meanwhile, the exclusion criteria were failure to complete the questionnaires and the presence of any mental disorders or physical illness in the parents that prevented their participation in the study. The instrument used included the palliative care quality questionnaire. This questionnaire has 15 items and 4 dimensions (communication with family, family participation, information sharing among health workers, support of siblings), the answer to each item includes a range of scores from 0 (never) to 4 (always), and the total score ranges from 0 to 100. After entering the data into the SPSS software, version 22, the data were analyzed using descriptive statistical tests.
Results The average age of the parents was 37.83±5.86 years. The average quality of palliative care score for children with cancer was 29.54±0.34. The lowest average score was related to the dimension of supporting siblings (4.1±0.34). 
Conclusion The quality of palliative care provided to children with cancer is lower than average and needs more attention in some aspects, especially the support of siblings. Accordingly, it is recommended to provide proper planning to improve these dimensions and provide high-quality palliative care in this population.