C. Morris

发表

Mapping epilepsy-specific patient-reported outcome measures for children to a proposed core outcome set for childhood epilepsy

H. Crudgington, A. Collingwood, L. Bray, 2020, Epilepsy & Behavior.

Core Health Outcomes in Childhood Epilepsy (CHOICE): Development of a core outcome set using systematic review methods and a Delphi survey consensus

B. Carter, D. Hughes, Morwenna Rogers, 2019, Epilepsia.

Public involvement in health research: what does ‘good’ look like in practice?

K. Boddy, G. Bjornstad, C. Morris, 2020, Research Involvement and Engagement.

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

Stuart Logan, Ruth Garside, Michelle Richardson, 2015, Health technology assessment.

Informing the NHS Outcomes Framework: evaluating meaningful health outcomes for children with neurodisability using multiple methods including systematic review, qualitative research, Delphi survey and consensus meeting

A. Tennant, S. Logan, B. Beresford, 2014 .

Epilepsy‐specific patient‐reported outcome measures of children's health‐related quality of life: A systematic review of measurement properties

Morwenna Rogers, H. Crudgington, P. Gringras, 2020, Epilepsia.

Sleep positioning systems for children and adults with a neurodisability: A systematic review

Morwenna Rogers, J. Thompson‐Coon, C. Morris, 2018, British Journal of Occupational Therapy.

Towards a shared vision for measureable and meaningful health outcomes for children and young people with neurodisability: qualitative research, Delphi survey, systematic review, and stakeholder prioritisation

A. Tennant, S. Logan, B. Beresford, 2015, Trials.

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

S. Logan, C. Morris, V. Shilling, 2015, Child: care, health and development.

A systematic review of generic multidimensional patient-reported outcome measures for children, part I: descriptive characteristics.

A. Tennant, S. Logan, J. Thompson Coon, 2015, Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research.

Query Reference Query Q 10

B. Beresford, C. Morris, V. Shilling, 2022 .

Search strategy used for review 2

Stuart Logan, Ruth Garside, Obioha C. Ukoumunne, 2015 .

Example of a completed qualitative data extraction form for review 3

Christopher Morris, Ruth Garside, Obioha C. Ukoumunne, 2015 .

Example of concept map (review 4a)

Christopher Morris, Ruth Garside, Obioha C. Ukoumunne, 2015 .

Search strategy used for reviews 3 and 4

Stuart Logan, Ruth Garside, Christopher Morris, 2015 .

Additional information on Chapter 4 search methodology

Shannon Robalino, Caroline B. Terwee, James Law, 2015 .

Online community engagement in response to COVID‐19 pandemic

H. Kuper, M. Heys, A. Hayward, 2021, Health expectations : an international journal of public participation in health care and health policy.

Working with Patients and Members of the Public: Informing Health Economics in Child Health Research

J. Ingram, C. Morris, A. Hawton, 2018, PharmacoEconomics - Open.

Autism and primary care dentistry: parents’ experiences of taking children with autism or working diagnosis of autism for dental examinations

D. Moles, C. Morris, S. Blake, 2018, International journal of paediatric dentistry.

Consensus meeting participants

A. Tennant, S. Logan, B. Beresford, 2014 .

Meeting the Information Needs of Families of Children with Chronic Health Conditions

C. Morris, V. Shilling, C. McHugh, 2013, Physical & occupational therapy in pediatrics.

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

M. Richardson, T. Ford, K. Stein, 2015, Health expectations : an international journal of public participation in health care and health policy.

Implementation of training to improve communication with disabled children on the ward: A feasibility study

S. Logan, C. Morris, H. Hambly, 2021, Health expectations : an international journal of public participation in health care and health policy.

GRIPP2 reporting checklists: tools to improve reporting of patient and public involvement in research

D. G. Altman, D. Moher, D. Altman, 2017, Research Involvement and Engagement.

Parents Suggest Which Indicators of Progress and Outcomes Should be Measured in Young Children with Autism Spectrum Disorder

Geraldine Macdonald, Bryony Beresford, Paul Gringras, 2017, Journal of autism and developmental disorders.

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

S. Logan, C. Morris, H. Hambly, 2017, BMJ Paediatrics Open.

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

S. Logan, S. Sharkey, C. Morris, 2016, Health expectations : an international journal of public participation in health care and health policy.

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

Morwenna Rogers, C. Morris, V. Shilling, 2012, Child: care, health and development.

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

C. Abraham, M. Tarrant, C. Morris, 2014, Developmental medicine and child neurology.

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

S. Logan, O. Ukoumunne, Morwenna Rogers, 2013, Developmental medicine and child neurology.

Towards a definition of neurodisability: a Delphi survey

S. Logan, C. Morris, A. Janssens, 2013, Developmental medicine and child neurology.

GRIPP2 reporting checklists: tools to improve reporting of patient and public involvement in research

D G Altman, P Littlejohns, S Staniszewska, 2017, British Medical Journal.

Systematic review of tools to measure outcomes for young children with autism spectrum disorder.

G. Baird, Jonathan Green, H. McConachie, 2015, Health technology assessment.

Improving continence in children and young people with neurodisability: a systematic review and survey.

S. Logan, J. Thompson Coon, Morwenna Rogers, 2021, Health Technology Assessment.

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

K Boddy, K. Boddy, C. Morris, 2015, Child: care, health and development.

Parent-to-parent support interventions for parents of babies cared for in a neonatal unit—protocol of a systematic review of qualitative and quantitative evidence

K. Boddy, R. Whear, J. Thompson‐Coon, 2018, Systematic Reviews.

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.

Karen N. Allen, A. Tennant, S. Logan, 2015, Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research.

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

S. Logan, C. Morris, V. Shilling, 2015, Child: care, health and development.

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

A. Tennant, C. Jenkinson, S. Logan, 2015, Developmental medicine and child neurology.

Quality of Life Measurement in Neurodegenerative and Related Conditions: Aspects of methodology relevant to patient-reported outcome measures (PROMs)

C. Jenkinson, J. Dawson, C. Morris, 2011 .

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

Charles Abraham, Christopher Morris, Megan Armstrong, 2017, Disability and rehabilitation.

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

C. Abraham, M. Tarrant, O. Ukoumunne, 2016, Disability and rehabilitation.

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

P. Williamson, B. Carter, D. Hughes, 2017, Trials.

Community-based family and carer-support programmes for children with disabilities

H. Kuper, M. Heys, C. Morris, 2020, Paediatrics and Child Health.

Sleep positioning systems for children with cerebral palsy.

S. Logan, Morwenna Rogers, J. Thompson‐Coon, 2015, The Cochrane database of systematic reviews.

Sleep positioning for children with cerebral palsy (Protocol)

S. Logan, Morwenna Rogers, J. Thompson‐Coon, 2014 .

Sleep positioning for children with cerebral palsy

S. Logan, Morwenna Rogers, J. Thompson‐Coon, 2011 .

Engaging stakeholders in rehabilitation research: a scoping review of strategies used in partnerships and evaluation of impacts

D. Russell, Tram Nguyen, C. Camden, 2015, Disability and rehabilitation.

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

C. Abraham, M. Tarrant, C. Morris, 2017, Disability and health journal.

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

Charles Abraham, Christopher Morris, Megan Armstrong, 2015, Disability and rehabilitation.

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

A. Tennant, S. Logan, B. Beresford, 2015, Health and Quality of Life Outcomes.

Setting research priorities to improve the health of children and young people with neurodisability: a British Academy of Childhood Disability-James Lind Alliance Research Priority Setting Partnership

M. Fenton, D. Simkiss, K. Cowan, 2015, BMJ Open.

Healthy Parent Carers: feasibility randomised controlled trial of a peer-led group-based health promotion intervention for parent carers of disabled children.

M. Tarrant, S. Logan, O. Ukoumunne, 2021, Pilot and Feasibility Studies.

Healthy Parent Carers programme: mixed methods process evaluation and refinement of a health promotion intervention

M. Tarrant, S. Logan, Aleksandra J. Borek, 2021, BMJ Open.

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

S. Logan, C. Morris, A. Hawton, 2015 .

The Connection between Personality Traits and Perceived Stress: An In-Depth Look at How Personality Traits Can Influence Perceived Stress during an Immersion Study in a Developing Nation

C. Morris, 2015 .

Healthy Parent Carers programme: development and feasibility of a novel group-based health-promotion intervention

S. Logan, Aleksandra J. Borek, G. Bjornstad, 2018, BMC Public Health.

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

C. Morris, K. Wyatt, V. Shilling, 2011, Developmental medicine and child neurology.

Reaching consensus on reporting patient and public involvement (PPI) in research: methods and lessons learned from the development of reporting guidelines

Iveta Simera, David Moher, Colin Tysall, 2017, BMJ Open.

Health outcomes for children with neurodisability: what do professionals regard as primary targets?

S. Logan, C. Morris, A. Janssens, 2014, Archives of Disease in Childhood.

Key health outcomes for children and young people with neurodisability: qualitative research with young people and parents

B. Beresford, C. Morris, V. Shilling, 2014, BMJ Open.

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

M. Tarrant, S. Logan, O. Ukoumunne, 2021, Pilot and Feasibility Studies.

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

M. Tarrant, S. Logan, O. Ukoumunne, 2019, Pilot and Feasibility Studies.

Healthy Parent Carers: Acceptability and practicability of online delivery and learning through implementation by delivery partner organisations

M. Tarrant, S. Logan, Aleksandra J. Borek, 2023, Health expectations : an international journal of public participation in health care and health policy.