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Staff Profile

Dr Chris Morris

Associate Professor in Child Health Research

Kath Maguire

I lead the research unit PenCRU, which undertakes a programme of applied health services research aimed at identifying ways to improve the health and wellbeing of disabled children and their families and seeks funding to carry out specific major research projects. The goals of PenCRU are consistent with the broader mission of PenCLAHRC, whilst being focused on childhood disability research. PenCRU involves families of disabled children as partners in all the activities of the unit through our Family Faculty. The vision for PenCRU is to work in partnership with families, clinicians and commissioners as the principal users of our research findings. 

Email me

Contact by phone
01392 262980

Employed by
University of Exeter

Areas of expertise
Child Health

Projects

Non pharmacological interventions for Attention-Deficit/Hyperactivity Disorder (ADHD) delivered in school settings: a systematic review of quantitative and qualitative research

Peer Support

CHUMS

What are the benefits and costs of providing peer support to parents of disabled children?

Sleep positioning for children with cerebral palsy: a systematic review

Non-pharmacological interventions for Attention-Deficit/Hyperactivity Disorder (ADHD) in school settings

Changing Agendas on Sleep, Treatment and Learning in Epilepsy - A long term condition of children (CASTLE)

Hospital Communications

Parent-to-Parent Support Interventions for Parents of Babies Cared for in a Neonatal unit (PaReNt)

Informing the NHS outcomes framework: what outcomes of NHS care should be measured for children with neurodisability?

Improving continence in children and young people with neurodisability (ICoN study)

Healthy Parent Carers

Understanding research priorities for young people with long term health conditions

Publications

Why it is crucial to involve families in all stages of childhood disability research

Peer support for parents of children with chronic disabling conditions: a systematic review of quantitative and qualitative studies

Meeting the Information Needs of Families of children with chronic health conditions

Towards a definition of neurodisability: a Delphi survey

Communicating with disabled children when inpatients: Barriers and facilitators identified by parents and professionals in a qualitative study

Involving disabled children and young people as partners in research: a systematic review

A Systematic Review of Generic Multidimensional Patient-Reported Outcome Measures for Children, Part I: Descriptive Characteristics

A Systematic Review of Generic Multidimensional Patient-Reported Outcome Measures for Children, Part II: Evaluation of Psychometric Performance of English-Language Versions in a General Population

Meaningful health outcomes for paediatric neurodisability: stakeholder prioritisation and appropriateness of patient reported outcome measures

Development of the Oxford ankle foot questionnaire: finding out how children are affected by foot and ankle problems

Resources for parents raising a disabled child in the UK

Peer support for parents of disabled children part 2: how organizational and process factors influence shared experience in a one-to-one service, a qualitative study

Meaningful health outcomes for paediatric neurodisability: Stakeholder prioritisation and appropriateness of patient reported outcome measures.

Core Health Outcomes In Childhood Epilepsy (CHOICE): protocol for the selection of a core outcome set

Children's contact with people with disabilities and their attitudes towards disability: a cross-sectional study

Rasch analysis of the Chedoke-McMaster Attitudes towards Children with Handicaps scale

"Interventions utilising contact with people with disabilities to improve children's attitudes towards disability: A systematic review and meta-analysis"

What are the benefits and costs of providing peer support to parents of disabled children

The experience of disabled children as inpatients: a structured review and synthesis of qualitative studies reporting the views of children, parents and professionals

Sleep positioning for children with cerebral palsy (Protocol)

The association between children’s contact with people with disabilities and their attitudes towards disability: a systematic review

Peer support for parents of disabled children part 1: perceived outcomes of a one-to-one service, a qualitative study

Peer support for parents of disabled children part 1: perceived outcomes of a one-to-one service, a qualitative study.

Improving communication between staff and disabled children in hospital wards: testing the feasibility of a training intervention developed through intervention mapping

Variation in referral and access to new psychological therapy services by age: an empirical quantitative study

End-user involvement in a systematic review of quantitative and qualitative research of non-pharmacological interventions for attention deficit hyperactivity disorder (ADHD) delivered in school settings: reflections on the impacts and challenges.

Sleep positioning for children with cerebral palsy

Measurement properties of multidimensional patient-reported outcome measures in neurodisability: a systematic review of evaluation studies

Non-pharmacological interventions for attention-deficit/hyperactivity disorder (ADHD) delivered in school settings: systematic reviews of quantitative and qualitative research

Healthy Parent Carers peer-led group-based health promotion intervention for parent carers of disabled children: protocol for a feasibility study using a parallel group randomised controlled trial design

Upcoming Events

Apr
16

Searching and Review Clinic

Online appointments via Microsoft Teams

COVID-19 update: Following advice issued to all University of Exeter staff on Monday 16th March to work...
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Apr
21

PPI Advice Clinic - POSTPONED

South Cloisters, St Luke's Campus, University of Exeter

Patient and Public Involvement Advice Clinics Held every month 30 minutes between 12pm-1pm Whatever your query, from finding...
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Calendar

News

Understanding research priorities for young people with long term health conditions

10 March 2020

A collaboration between researchers has resulted in a clearer understanding of how to address the...
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PenARC welcomes new PhD students

18 February 2020

Our PhD studentships are linked to PenARC project and priority areas and are an important...
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Groundbreaking role for operational research in NHS decision-making

12 February 2020

A pioneering collaboration between PenARC and University Hospitals Plymouth NHS Trust (UHP) has led to...
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News

Research Projects

Understanding research priorities for young people with long term health conditions

Theme: ARC - Complex Care

A project to identify and describe, through patient and public involvement activities, the research needs of...
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Getting Up Following a Fall

Theme: ARC - Complex Care

Although there is evidence that falls can be prevented, little attention has been paid to...
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Research Projects