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      Complex care for kids Ontario: protocol for a mixed-methods randomised controlled trial of a population-level care coordination initiative for children with medical complexity

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          Abstract

          Introduction

          Technological and medical advances have led to a growing population of children with medical complexity (CMC) defined by substantial medical needs, healthcare utilisation and morbidity. These children are at a high risk of missed, fragmented and/or inappropriate care, and families bear extraordinary financial burden and stress. While small in number (<1% of children), this group uses ~1/3 of all child healthcare resources, and need coordinated care to optimise their health. Complex care for kids Ontario (CCKO) brings researchers, families and healthcare providers together to develop, implement and evaluate a population-level roll-out of care for CMC in Ontario, Canada through a randomised controlled trial (RCT) design. The intervention includes dedicated key workers and the utilisation of coordinated shared care plans.

          Methods and analysis

          Our primary objective is to evaluate the CCKO intervention using a randomised waitlist control design. The waitlist approach involves rolling out an intervention over time, whereby all participants are randomised into two groups (A and B) to receive the intervention at different time points determined at random. Baseline measurements are collected at month 0, and groups A and B are compared at months 6 and 12. The primary outcome is the family-prioritized Family Experiences with Coordination of Care (FECC) survey at 12 months. The FECC will be compared between groups using an analysis of covariance with the corresponding baseline score as the covariate. Secondary outcomes include reports of child and parent health outcomes, health system utilisation and process outcomes.

          Ethics and dissemination

          Research ethics approval has been obtained for this multicentre RCT. This trial will assess the effect of a large population-level complex care intervention to determine whether dedicated key workers and coordinated care plans have an impact on improving service delivery and quality of life for CMC and their families.

          Trial registration number

          NCT02928757.

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          Most cited references38

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          Subjective well-being: The science of happiness and a proposal for a national index.

          Ed Diener (2000)
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            Measurement of health status. Ascertaining the minimal clinically important difference.

            In recent years quality of life instruments have been featured as primary outcomes in many randomized trials. One of the challenges facing the investigator using such measures is determining the significance of any differences observed, and communicating that significance to clinicians who will be applying the trial results. We have developed an approach to elucidating the significance of changes in score in quality of life instruments by comparing them to global ratings of change. Using this approach we have established a plausible range within which the minimal clinically important difference (MCID) falls. In three studies in which instruments measuring dyspnea, fatigue, and emotional function in patients with chronic heart and lung disease were applied the MCID was represented by mean change in score of approximately 0.5 per item, when responses were presented on a seven point Likert scale. Furthermore, we have established ranges for changes in questionnaire scores that correspond to moderate and large changes in the domains of interest. This information will be useful in interpreting questionnaire scores, both in individuals and in groups of patients participating in controlled trials, and in the planning of new trials.
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              Children with medical complexity: an emerging population for clinical and research initiatives.

              Children with medical complexity (CMC) have medical fragility and intensive care needs that are not easily met by existing health care models. CMC may have a congenital or acquired multisystem disease, a severe neurologic condition with marked functional impairment, and/or technology dependence for activities of daily living. Although these children are at risk of poor health and family outcomes, there are few well-characterized clinical initiatives and research efforts devoted to improving their care. In this article, we present a definitional framework of CMC that consists of substantial family-identified service needs, characteristic chronic and severe conditions, functional limitations, and high health care use. We explore the diversity of existing care models and apply the principles of the chronic care model to address the clinical needs of CMC. Finally, we suggest a research agenda that uses a uniform definition to accurately describe the population and to evaluate outcomes from the perspectives of the child, the family, and the broader health care system.
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                Author and article information

                Journal
                BMJ Open
                BMJ Open
                bmjopen
                bmjopen
                BMJ Open
                BMJ Publishing Group (BMA House, Tavistock Square, London, WC1H 9JR )
                2044-6055
                2019
                1 August 2019
                : 9
                : 8
                : e028121
                Affiliations
                [1 ] departmentDivision of Pediatric Medicine , The Hospital for Sick Children , Toronto, Ontario, Canada
                [2 ] departmentDepartment of Pediatrics , University of Toronto , Toronto, Ontario, Canada
                [3 ] departmentChild Health Evaluative Sciences , The Hospital for Sick Children , Toronto, Ontario, Canada
                [4 ] departmentSchool of Rehabilitation Therapy , Queen’s University , Kingston, Ontario, Canada
                [5 ] departmentInstitute of Health Policy, Management and Evaluation , University of Toronto Dalla Lana School of Public Health , Toronto, Ontario, Canada
                [6 ] departmentDepartment of Paediatrics , Children’s Hospital of Eastern Ontario , Ottawa, Ontario, Canada
                [7 ] departmentDepartment of Pediatrics , Hamilton Health Sciences Center, McMaster University , Hamilton, Ontario, Canada
                [8 ] departmentDepartment of Pediatrics , Western University , London, Ontario, Canada
                [9 ] departmentClinical Trials Unit , The Hospital for Sick Children, University of Toronto , Toronto, Ontario, Canada
                [10 ] departmentThe Provincial Council for Maternal and Child Health , The Hospital for Sick Children , Toronto, Ontario, Canada
                [11 ] Institute for Clinical Evaluative Sciences , Toronto, Ontario, Canada
                [12 ] departmentDepartment of Pediatrics , Royal Victoria Regional Health Centre , Barrie, Ontario, Canada
                [13 ] departmentDepartment of Pediatrics , North York General Hospital, University of Toronto , Toronto, Ontario, Canada
                [14 ] departmentThe Credit Valley Hospital , Trillium Health Partners , Mississauga, Ontario, Canada
                [15 ] Peterborough Regional Health Centre , Peterborough, Ontario, Canada
                [16 ] departmentDepartment of Pediatrics , Orillia Soldier’s Memorial Hospital , Orillia, Ontario, Canada
                [17 ] departmentDepartment of Pediatrics , Michael Garron Hospital , Toronto, Ontario, Canada
                Author notes
                [Correspondence to ] Dr. Julia Orkin; julia.orkin@ 123456sickkids.ca
                Article
                bmjopen-2018-028121
                10.1136/bmjopen-2018-028121
                6688698
                31375613
                4c66b8ff-e9b0-4aa8-b365-cc671a56576b
                © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

                This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.

                History
                : 22 November 2018
                : 20 March 2019
                : 24 May 2019
                Funding
                Funded by: Ontario Strategy for Patient-Oriented Research Support Unit IMPACT (Innovative, Measurable, Patient-oriented, Appropriate, Collaborative and Transformative) Award;
                Funded by: Canadian Institute of Health Research;
                Categories
                Paediatrics
                Protocol
                1506
                1719
                Custom metadata
                unlocked

                Medicine
                complex care,medical complexity,health services,children,randomized controlled trial,parents
                Medicine
                complex care, medical complexity, health services, children, randomized controlled trial, parents

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