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Claire Glasscoe

Biographic Data

ID7357219
NAMEClaire Glasscoe
GIVEN NAMESClaire
FAMILY NAMEGlasscoe
SIGNATUREGLASSCOE C
AFFILIATIONSDepartment of Women’s and Children’s Health, Institute of Translational Medicine, University of Liverpool, Alder Hey Children’s NHS Foundation Trust
VERIFIEDNo
TOTAL WORKS2
TOTAL CITATIONS0
WORKS AS AUTHOR2
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2023
LATEST PUBLICATION YEAR2025
H-INDEX0
  • Development and validation of a short form psychometric tool assessing the caregiving Challenge of Living with Cystic Fibrosis (CLCF-SF) in a child

    Open Access•Gareth McCray, Holly Hope et al.•ARTICLE•Psychology & Health•2025

    Objective Caring for a child with cystic fibrosis (CF) is a rigorous daily commitment for caregivers and treatment burden is a major concern. We aimed to develop and validate a short form version of a 46-item tool assessing the Challenge of Living with Cystic Fibrosis (CLCF) for clinical or research use.Design A novel genetic algorithm based on ‘evolving’ a subset of items from a pre-specified set of criteria, was applied to optimise the tool, us…

  • Development and preliminary validation of the challenges of living with cystic fibrosis (CLCF) questionnaire

    Open Access•Claire Glasscoe, Holly Hope et al.•ARTICLE•Psychology & Health•2023

    OBJECTIVE: Treatments for cystic fibrosis (CF) are complex, labour-intensive, and perceived as highly burdensome by caregivers of children with CF. An instrument assessing burden of care is needed. DESIGN: A stepwise, qualitative design was used to create the CLCF with caregiver focus groups, participant researchers, a multidisciplinary professional panel, and cognitive interviews. MAIN OUTCOME MEASURES: ). RESULTS: = 0.002). CONCLUSIONS: The CLC…

No prominent works on this page.

  • Development and preliminary validation of the challenges of living with cystic fibrosis (CLCF) questionnaire

    Open Access•Claire Glasscoe, Holly Hope et al.•ARTICLE•Psychology & Health•2023

    OBJECTIVE: Treatments for cystic fibrosis (CF) are complex, labour-intensive, and perceived as highly burdensome by caregivers of children with CF. An instrument assessing burden of care is needed. DESIGN: A stepwise, qualitative design was used to create the CLCF with caregiver focus groups, participant researchers, a multidisciplinary professional panel, and cognitive interviews. MAIN OUTCOME MEASURES: ). RESULTS: = 0.002). CONCLUSIONS: The CLC…

  • Development and validation of a short form psychometric tool assessing the caregiving Challenge of Living with Cystic Fibrosis (CLCF-SF) in a child

    Open Access•Gareth McCray, Holly Hope et al.•ARTICLE•Psychology & Health•2025

    Objective Caring for a child with cystic fibrosis (CF) is a rigorous daily commitment for caregivers and treatment burden is a major concern. We aimed to develop and validate a short form version of a 46-item tool assessing the Challenge of Living with Cystic Fibrosis (CLCF) for clinical or research use.Design A novel genetic algorithm based on ‘evolving’ a subset of items from a pre-specified set of criteria, was applied to optimise the tool, us…

Clinical Psychology (2 works) · Convergent validity (2 works) · Cronbach's alpha (2 works) · Cystic fibrosis (2 works) · Cystic Fibrosis Research Advances (2 works) · Family and Disability Support Research (2 works) · Internal consistency (2 works) · Medicine (2 works) · Psychology (2 works) · Psychometrics (2 works)

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