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Laurel Mimmo

Showing results (11-20 of 21) with videos related to

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Value in Health : the Journal of the International Society for Pharmacoeconomics and Outcomes Research|June 6, 2024
Measuring Healthcare Experiences Among People With Intellectual Disability: A Rapid Evidence Synthesis of Tools and MethodsReema Harrison, Corey Adams, Bronwyn Newman, et al.
Children (Basel, Switzerland)|December 24, 2021
What Are the Psycho-Social and Information Needs of Adolescents and Young Adults Cancer Care Consumers with Intellectual Disability? A Systematic Review of Evidence with Recommendations for Future Research and PracticeÉidín Ní Shé, Fiona E J McDonald, Laurel Mimmo, et al.
BMJ Open|December 7, 2021
Codesigning patient experience measures for and with children and young people with intellectual disability: a study protocolLaurel Mimmo, Susan Woolfenden, Joanne Travaglia, et al.
BMC Health Services Research|December 6, 2022
Evaluating clinician experience in value-based health care: the development and validation of the Clinician Experience Measure (CEM)Reema Harrison, Elizabeth Manias, Louise Ellis, et al.
Clinical Child and Family Psychology Review|February 24, 2026
Procedural Support for Neurodivergent Children During Medical Procedures: A Scoping ReviewMari Takashima, Harriet Robertson, Karin Plummer, et al.
Health Expectations : an International Journal of Public Participation in Health Care and Health Policy|January 23, 2026
Co-Producing a Patient Reported Experience Measure (PREM) With and for People With Intellectual DisabilityBronwyn Newman, Ling Wu, Laurel Mimmo, et al.
BMJ Open|April 6, 2023
Codesigning a social prescribing pathway to address the social determinant of health concerns of children with cerebral palsy and their families in Australia: a protocol for a mixed-methods formative research studyKatarina Ostojic, Simon Paget, Tanya Martin, et al.
Disability and Rehabilitation|August 19, 2024
A qualitative study investigating the experiences of unmet social needs for children with cerebral palsy and their families: perspectives of parents and cliniciansKatarina Ostojic, Isra Karem, Simon Paget, et al.
BMJ Open|July 13, 2024
EPIC-CP pilot trial study protocol: a multicentre, randomised controlled trial investigating the feasibility and acceptability of social prescribing for Australian children with cerebral palsyKatarina Ostojic, Isra Karem, Simon Paget, et al.
Health Expectations : an International Journal of Public Participation in Health Care and Health Policy|August 30, 2025
Co-Producing Patient-Reported Experience Measures With People With Intellectual Disability to Improve Healthcare Quality and Outcomes: The 'Listen to Me' Project ProtocolReema Harrison, Bronwyn Newman, Beth Catlett, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Value in Health : the Journal of the International Society for Pharmacoeconomics and Outcomes Research|June 6, 2024
Measuring Healthcare Experiences Among People With Intellectual Disability: A Rapid Evidence Synthesis of Tools and MethodsReema Harrison, Corey Adams, Bronwyn Newman, et al.
Children (Basel, Switzerland)|December 24, 2021
What Are the Psycho-Social and Information Needs of Adolescents and Young Adults Cancer Care Consumers with Intellectual Disability? A Systematic Review of Evidence with Recommendations for Future Research and PracticeÉidín Ní Shé, Fiona E J McDonald, Laurel Mimmo, et al.
BMJ Open|December 7, 2021
Codesigning patient experience measures for and with children and young people with intellectual disability: a study protocolLaurel Mimmo, Susan Woolfenden, Joanne Travaglia, et al.
BMC Health Services Research|December 6, 2022
Evaluating clinician experience in value-based health care: the development and validation of the Clinician Experience Measure (CEM)Reema Harrison, Elizabeth Manias, Louise Ellis, et al.
Clinical Child and Family Psychology Review|February 24, 2026
Procedural Support for Neurodivergent Children During Medical Procedures: A Scoping ReviewMari Takashima, Harriet Robertson, Karin Plummer, et al.
Health Expectations : an International Journal of Public Participation in Health Care and Health Policy|January 23, 2026
Co-Producing a Patient Reported Experience Measure (PREM) With and for People With Intellectual DisabilityBronwyn Newman, Ling Wu, Laurel Mimmo, et al.
BMJ Open|April 6, 2023
Codesigning a social prescribing pathway to address the social determinant of health concerns of children with cerebral palsy and their families in Australia: a protocol for a mixed-methods formative research studyKatarina Ostojic, Simon Paget, Tanya Martin, et al.
Disability and Rehabilitation|August 19, 2024
A qualitative study investigating the experiences of unmet social needs for children with cerebral palsy and their families: perspectives of parents and cliniciansKatarina Ostojic, Isra Karem, Simon Paget, et al.
BMJ Open|July 13, 2024
EPIC-CP pilot trial study protocol: a multicentre, randomised controlled trial investigating the feasibility and acceptability of social prescribing for Australian children with cerebral palsyKatarina Ostojic, Isra Karem, Simon Paget, et al.
Health Expectations : an International Journal of Public Participation in Health Care and Health Policy|August 30, 2025
Co-Producing Patient-Reported Experience Measures With People With Intellectual Disability to Improve Healthcare Quality and Outcomes: The 'Listen to Me' Project ProtocolReema Harrison, Bronwyn Newman, Beth Catlett, et al.
Pageof 3