Development of an EORTC Patient-Reported Outcome (PRO) Questionnaire for Quality of Life (QOL) of children with cancer: Phase I & II

Study ID: 48875
Short Title: Development of an EORTC QOL Child Questionnaire
Trust Name: UHS
Recruitment Site: Southampton General Hospital
Disease Area: CYP
Phase: N/A
Expected End Date: 31/01/2024
Postcode: SO16 6YD
Contact Name: Amanda Pattie
Contact Email: studysupport1and3.crnwessex@nihr.ac.uk
Active: Yes

Inclusion criteria, exclusion criteria and study summary

The age group above relates to child participants (not parents or HCPs). Inclusion criteria: Diagnosis of any cancer and receiving treatment for cancer or palliative / supportive care Aged between 8 - 14 years No cognitive impairment Fluency in the native language of the local recruiting centre Willingness and ability of parents or guardians to give their fully informed consent Willingness and ability of children to give their assent HCPs: At least 5 years of clinical experience in paediatric oncology

Children with cognitive impairment and not able to give their assent or understand the nature of the study. Children / parents who are not willing to give their assent / consent. Children who have finished curative intent treatment and no longer have active disease.

The assessment of quality of life (HRQOL) is a critical outcome measure for trials evaluating the risks and benefits of treatments for children with cancer. QOL assessment also plays an important role within clinical practice by facilitating communication between children, their parents and clinicians. It is therefore vital that QOL measures include questions which are of significance to children with cancer. While several paediatric QOL measures exist, previous research has identified shortcomings of those questionnaires when applied to children with cancer. The European Organisation for Research and Treatment of Cancer Quality of Life Group (EORTC QLG) has an international reputation for the development of cancer QOL questionnaires with a core quality of life questionnaire (EORTC QLQ-C30) and supplementary modules specific to a particular tumour, condition or age group (older adults, adolescents and young adults). There is currently no EORTC QLG questionnaire specific to children. The objective of this multi-centre study is to use EORTC QLG guidelines to develop a measure asking about QOL concerns of relevance and importance to children aged 8-14 years with cancer and identify optimal response options which are appropriate for this age group. The study is led by the Medical University in Innsbruck, Austria and involves two phases: Phase I consists of a literature review as well as qualitative semi-structured interviews with 60 children (8-14 years), 45 parents and 30 health-care professionals (HCPs). In Phase Ib, a further 60 children (8-14 years) will be interviewed to evaluate the best response format (Smiley faces- vs. Likert-Scale) for these age groups. In Phase II, the issues generated in Phase I will be operationalized and transformed into items and a preliminary questionnaire for children with cancer of 8-14 years will be constructed. In the UK a total of 30 children, 20 parents and 5 HCPs will be recruited.

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