Literature DB >> 31652387

Development of the Melanoma Concerns Questionnaire (MCQ-28); refinement of the EORTC QLQ-MEL38 module.

Julie Winstanley1,2, Edward White2,3, Robyn Saw4, Teresa Young5, Bryan Burmeister6, Dejan Nikolic7,8, Iria Busto-Cornide9, Nicolás Iglesias-Pena10, Frances Boyle1,4.   

Abstract

OBJECTIVE: Few patient-reported outcome measures (PROMs) have been developed that adequately measure the patient-experience following diagnosis and treatment of melanoma. Building on previous research, which developed the European Organisation for Research and Treatment of Cancer (EORTC) Quality of Life Module (QLQ-MEL38), the aim of this study was to further test the hypothesised domain structure and psychometric properties of the phase 3 module, in a new larger sample of melanoma patients.
METHODS: Melanoma patients (n = 270) were recruited from four countries (Australia, England, Serbia, and Spain). Patients completed the EORTC core questionnaire (QLQ-C30), the QLQ-MEL38, and a sociodemographic survey. Using this new larger dataset, comparisons were made with the hypothesised domain structure of the EORTC phase 3 module using principal component analysis. Items which formed subscales in a revised domain structure were then tested for goodness of fit (GoF) to the Rasch model.
RESULTS: The original hypothesised and final domain structures were similar but not identical. Twenty-four items (83%) loaded onto the same distinct subscales previously generated by phase 3, and item-by-item comparison of the two pattern matrices indicated an extremely close match. Ten items were removed from the QLQ-MEL38 phase 3 module, and rescoring of some items was required. Four subscales, together with five individual items, comprised the final instrument.
CONCLUSION: The newly developed measure (named the Melanoma Concerns Questionnaire; MCQ-28) was found to tap into several important psychosocial domains of concern to melanoma patients, particularly those being managed in "usual" clinic settings.
© 2019 John Wiley & Sons, Ltd.

Entities:  

Keywords:  cancer; melanoma; psychometrics; quality of life; reproducibility of results; surveys and questionnaires

Year:  2019        PMID: 31652387     DOI: 10.1002/pon.5251

Source DB:  PubMed          Journal:  Psychooncology        ISSN: 1057-9249            Impact factor:   3.894


  2 in total

1.  Implementation of patient-reported outcome measures and patient-reported experience measures in melanoma clinical quality registries: a systematic review.

Authors:  Zachary Blood; Anh Tran; Lauren Caleo; Robyn Saw; Mbathio Dieng; Mark Shackleton; H Peter Soyer; Chris Arnold; Graham J Mann; Rachael L Morton
Journal:  BMJ Open       Date:  2021-02-11       Impact factor: 2.692

2.  Assessment of the perceived burden associated with Malignant Melanoma with Pictorial Representation of Illness and Self Measure (PRISM) and Melanoma Concerns Questionnaire (MCQ-28).

Authors:  Alessandro Borghi; Maria Elena Flacco; Alberto Monti; Lucrezia Pacetti; Michela Tabanelli; Monica Corazza
Journal:  Support Care Cancer       Date:  2022-01-15       Impact factor: 3.359

  2 in total

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