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Roxanne Parslow

Biographic Data

ID6576897
NAMERoxanne Parslow
GIVEN NAMESRoxanne
FAMILY NAMEParslow
SIGNATUREPARSLOW R
AFFILIATIONSCentre for Academic Child Health University of Bristol Bristol UK
ORCID0000-0002-3612-7121
VERIFIEDYes
TOTAL WORKS3
TOTAL CITATIONS1
WORKS AS AUTHOR3
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2020
LATEST PUBLICATION YEAR2026
H-INDEX1
  • Further Development and Validation of a Measure of Compassionate Healthcare in Action

    Open Access•Samantha R Allen, Ellen Huish et al.•ARTICLE•Health Expectations•2026

    BACKGROUND: Compassionate Healthcare In Action (CHIA) is a new questionnaire to measure patient experiences of compassionate care, with a particular focus on observable behaviours. It has been designed to address gaps in currently available metrics. It is generalisable across healthcare contexts and has been developed with patient and public involvement throughout. The present study sought to build on earlier development to evaluate the CHIA's fa…

  • The importance of school in the management of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome ( ME / CFS )

    Open Access•Philippa Clery, Catherine Linney et al.•ARTICLE•Health & Social Care in the…•2022•Cited by: 1•References: 3

    Paediatric Myalgic Encephalomyelitis (ME)/Chronic Fatigue Syndrome (CFS) is a disabling condition. Schools play a key role in adolescents' experiences with managing ME/CFS. However, little is known about the experiences of adolescents with ME/CFS (and their families) in schools. This paper is an incidental qualitative study, which combines data from two independent ME/CFS studies: study 1 researched ethnic minority adolescents with ME/CFS; study …

  • Development of a conceptual framework to underpin a health-related quality of life outcome measure in paediatric chronic fatigue syndrome/myalgic encephalopathy (CFS/ME)

    Open Access•Roxanne Parslow, Roxanne M Parslow et al.•ARTICLE•Quality of Life Research•2020

    An interactive card ranking exercise worked well for adolescents aged 12-17 to elicit the most important outcomes to them and explore each domain in further detail. We developed a final conceptual framework of HRQoL that forms the basis of a new paediatric patient-reported outcome measure (PROM) in CFS/ME

  • The importance of school in the management of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome ( ME / CFS )

    Open Access•Philippa Clery, Catherine Linney et al.•ARTICLE•Health & Social Care in the…•2022•Cited by: 1•References: 3

    Paediatric Myalgic Encephalomyelitis (ME)/Chronic Fatigue Syndrome (CFS) is a disabling condition. Schools play a key role in adolescents' experiences with managing ME/CFS. However, little is known about the experiences of adolescents with ME/CFS (and their families) in schools. This paper is an incidental qualitative study, which combines data from two independent ME/CFS studies: study 1 researched ethnic minority adolescents with ME/CFS; study …

  • Development of a conceptual framework to underpin a health-related quality of life outcome measure in paediatric chronic fatigue syndrome/myalgic encephalopathy (CFS/ME)

    Open Access•Roxanne Parslow, Roxanne M Parslow et al.•ARTICLE•Quality of Life Research•2020

    An interactive card ranking exercise worked well for adolescents aged 12-17 to elicit the most important outcomes to them and explore each domain in further detail. We developed a final conceptual framework of HRQoL that forms the basis of a new paediatric patient-reported outcome measure (PROM) in CFS/ME

  • The importance of school in the management of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome ( ME / CFS )

    Open Access•Philippa Clery, Catherine Linney et al.•ARTICLE•Health & Social Care in the…•2022•Cited by: 1•References: 3

    Paediatric Myalgic Encephalomyelitis (ME)/Chronic Fatigue Syndrome (CFS) is a disabling condition. Schools play a key role in adolescents' experiences with managing ME/CFS. However, little is known about the experiences of adolescents with ME/CFS (and their families) in schools. This paper is an incidental qualitative study, which combines data from two independent ME/CFS studies: study 1 researched ethnic minority adolescents with ME/CFS; study …

  • Further Development and Validation of a Measure of Compassionate Healthcare in Action

    Open Access•Samantha R Allen, Ellen Huish et al.•ARTICLE•Health Expectations•2026

    BACKGROUND: Compassionate Healthcare In Action (CHIA) is a new questionnaire to measure patient experiences of compassionate care, with a particular focus on observable behaviours. It has been designed to address gaps in currently available metrics. It is generalisable across healthcare contexts and has been developed with patient and public involvement throughout. The present study sought to build on earlier development to evaluate the CHIA's fa…

Chronic fatigue syndrome (2 works) · Clinical Psychology (2 works) · Clinical Psychology (2 works) · Fibromyalgia and Chronic Fatigue Syndrome Research (2 works) · Focus group (2 works) · Medicine (2 works) · Psychiatry (2 works) · Psychology (2 works) · Qualitative research (2 works) · Resilience and Mental Health (2 works)

Ethnos_APP • Open Source Project • MIT License • Frontend v2.0.0 • Privacy and Cookies • API Documentation: api.ethnos.app/docs • API Source Code: GitHub • DOI: 10.5281/zenodo.17049435 • Frontend Source Code: GitHub • DOI: 10.5281/zenodo.17050053 • cruz.rio.br • Expectantes Misericordiae