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Staff Profile

Dr Chris Morris

Senior Research Fellow

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. PenCRU receives core funding through a grant from the UK charity Cerebra, and seeks further 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

The effects of elimination and supplementation diets on symptoms of ADHD

Peer Support

CHUMS

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

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

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

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

Sleep positioning for children with cerebral palsy: a systematic review

Hospital Communications

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.

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

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.

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

Sleep positioning for children with cerebral palsy

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

Upcoming Events

Dec
13

PPI Advice Clinic

ITTC Building, Plymouth Science Park, Derriford, Plymouth, PL6 8BX

Whatever your query, from finding out more about Patient and Public Involvement to creating a PPI...
More information

Jan
09

PPI Advice Clinic

The University of Exeter, St Luke's campus, South Cloisters

Patient and Public Involvement Clinic What? These clinics have been set up to help the PenCLAHRC PPI Team manage and respond...
More information

Calendar

News

Collaborative Action for the Delivery of Effective Person-Centred Coordinated Care

27 November 2017

A paper published in the journal Health Research Policy and Systems, reports on a tactic...
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Research Hopes to Improve Dental Visits for Children with Autism

21 November 2017

  Inspired by her own experience as a mum to child with autism, a dental hygienist...
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New Study Underpins the Future of Person Centred Care

15 November 2017

Health provision is moving away from disease-based models to person centred delivery. This study addresses...
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News

Research Projects

The Zone - Icebreak Personality Disorder Pathway Redesign.

Theme: Evidence for Policy and Practice

The aim of this project will be to assess the impact of a new treatment...
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Care Under Pressure

Theme: Mental Health & Dementia

Realist review of interventions to tackle healthcare professionals’ mental ill health and its impacts on...
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Research Projects