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Published in: Health and Quality of Life Outcomes 1/2015

Open Access 01-12-2015 | Research Article

Development and validation of the BRIGHTLIGHT Survey, a patient-reported experience measure for young people with cancer

Authors: Rachel M. Taylor, Lorna A. Fern, Anita Solanki, Louise Hooker, Anna Carluccio, Julia Pye, David Jeans, Tom Frere–Smith, Faith Gibson, Julie Barber, Rosalind Raine, Dan Stark, Richard Feltbower, Susie Pearce, Jeremy S. Whelan

Published in: Health and Quality of Life Outcomes | Issue 1/2015

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Abstract

Background

Patient experience is increasingly used as an indicator of high quality care in addition to more traditional clinical end–points. Surveys are generally accepted as appropriate methodology to capture patient experience. No validated patient experience surveys exist specifically for adolescents and young adults (AYA) aged 13–24 years at diagnosis with cancer. This paper describes early work undertaken to develop and validate a descriptive patient experience survey for AYA with cancer that encompasses both their cancer experience and age-related issues. We aimed to develop, with young people, an experience survey meaningful and relevant to AYA to be used in a longitudinal cohort study (BRIGHTLIGHT), ensuring high levels of acceptability to maximise study retention.

Methods

A three-stage approach was employed: Stage 1 involved developing a conceptual framework, conducting literature/Internet searches and establishing content validity of the survey; Stage 2 confirmed the acceptability of methods of administration and consisted of four focus groups involving 11 young people (14–25 years), three parents and two siblings; and Stage 3 established survey comprehension through telephone-administered cognitive interviews with a convenience sample of 23 young people aged 14–24 years.

Result

Stage 1: Two-hundred and thirty eight questions were developed from qualitative reports of young people’s cancer and treatment-related experience. Stage 2: The focus groups identified three core themes: (i) issues directly affecting young people, e.g. impact of treatment-related fatigue on ability to complete survey; (ii) issues relevant to the actual survey, e.g. ability to answer questions anonymously; (iii) administration issues, e.g. confusing format in some supporting documents. Stage 3: Cognitive interviews indicated high levels of comprehension requiring minor survey amendments.

Conclusion

Collaborating with young people with cancer has enabled a survey of to be developed that is both meaningful to young people but also examines patient experience and outcomes associated with specialist cancer care. Engagement of young people throughout the survey development has ensured the content appropriately reflects their experience and is easily understood. The BRIGHTLIGHT survey was developed for a specific research project but has the potential to be used as a TYA cancer survey to assess patient experience and the care they receive.
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Metadata
Title
Development and validation of the BRIGHTLIGHT Survey, a patient-reported experience measure for young people with cancer
Authors
Rachel M. Taylor
Lorna A. Fern
Anita Solanki
Louise Hooker
Anna Carluccio
Julia Pye
David Jeans
Tom Frere–Smith
Faith Gibson
Julie Barber
Rosalind Raine
Dan Stark
Richard Feltbower
Susie Pearce
Jeremy S. Whelan
Publication date
01-12-2015
Publisher
BioMed Central
Published in
Health and Quality of Life Outcomes / Issue 1/2015
Electronic ISSN: 1477-7525
DOI
https://doi.org/10.1186/s12955-015-0312-7

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