ArticleBMJ open2019
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.
Article in BMJ open, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT02928757 (Complex Care for Kids Ontario), which is not on this map. Cited by 11 papers, 1 of them a synthesis that pooled it.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Complex Care for Kids Ontario (CCKO): A Patient- and Family-centred Implementation and Evaluation of Care Coordination for Children With Medical Complexity
Who cites it
11 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Patient navigator programmes for children and adolescents with chronic diseases.The Cochrane database of systematic reviews · 2024Pooled it
- The impact of the Indiana Complex Care Coordination Collaborative (IC4) on caregivers of children with complex medical conditions.BMC pediatrics · 2026Article
- Competency-based training for paediatric residents caring for children with medical complexity.Paediatrics & child health · 2025Article
- Drivers that decrease hospital-delivered care in children with medical complexity: Parental perspectives.Paediatrics & child health · 2024Article
- Out-of-pocket expenses reported by families of children with medical complexity.Paediatrics & child health · 2024Article
- Evaluation of a Secure Messaging System in the Care of Children With Medical Complexity: Mixed Methods Study.JMIR formative research · 2023Article
- The impact of the COVID-19 pandemic on children with medical complexity.BMC pediatrics · 2022Article
- A Novel Hospital-to-Home System for Children With Medical Complexities: Usability Testing Study.JMIR formative research · 2022Article
- Research priorities for children with neurological impairment and medical complexity in high-income countries.Developmental medicine and child neurology · 2022Article
- Process Evaluation of a Hub-and-Spoke Model to Deliver Coordinated Care for Children with Medical Complexity across Ontario: Facilitators, Barriers and Lessons Learned.Healthcare policy = Politiques de sante · 2021Article
- Health Care Use and Costs of Children, Adolescents, and Young Adults With Somatic Symptom and Related Disorders.JAMA network open · 2020Article
Corrections and comments
- Erratum issuedCorrection:2019
Authors and funding
20 authors.
Funding
Abstract
introductionTechnological 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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Registered trials
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