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Complex Care for Kids Ontario (CCKO)

Complex Care for Kids Ontario (CCKO): A Patient- and Family-centred Implementation and Evaluation of Care Coordination for Children With Medical Complexity

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02928757
Enrollment
160
Registered
2016-10-10
Start date
2016-12-31
Completion date
2021-05-31
Last updated
2022-09-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Children With Medical Complexity

Keywords

Care coordination, Complex care kids Ontario, Technology-dependent, Quality of life

Brief summary

There are \ 6,200 children in Ontario with special and complex healthcare needs requiring multiple services from many different doctors and other healthcare providers. These children are at a high risk of missed, duplicated or inappropriate care, and extraordinary financial burden and stress on families. While small in number (\<1% of Ontario kids), these children use 1/3 of all child healthcare resources, and are known to desperately need coordinated care to optimize their health. Complex Care Kids Ontario (CCKO) brings together researchers, children and families, and healthcare providers from across Ontario to develop, implement and evaluate an evidence-based and coordinated model of care for every child with medical complexity in Ontario.

Interventions

OTHERComplex care clinic as part of the CCKO initiative

The CCKO intervention involves intensive care coordination, defined as: deliberate organization of patient care activities between two or more participants (including the patient) involved in a patient's care to facilitate the appropriate delivery of health care services. Organizing care involves marshaling of personnel and other resources needed to carry out all required patient care activities and is often managed by the exchange of information among participants responsible for different aspects of care. Within CCKO, intensive care coordination will specifically include: 1) the tailored, family/health care provider co-creation and regular updating of care coordination plans for each child which will be 2) facilitated and accounted for by key workers partnering with families.

Sponsors

Children's Hospital of Eastern Ontario
CollaboratorOTHER
London Health Sciences Centre
CollaboratorOTHER
Hamilton Health Sciences Corporation
CollaboratorOTHER
The Hospital for Sick Children
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
0 Years to 16 Years
Healthy volunteers
No

Inclusion criteria

(Meets at least ONE criterion from EACH of the following four conditions): * Technology dependent and/or users of high intensity care * Child is dependent on mechanical ventilators, and/or requires prolonged IV administration of nutritional substances or drugs and/or is to have prolonged dependence on other device-based support. For example: tracheostomy tube care/ artificial airway, suctioning, oxygen support, or tube feeding * Child has prolonged dependence on medical devices to compensate for vital bodily functions, and requires daily/ near daily nursing care, e.g., cardiorespiratory monitors; renal dialysis due to kidney failure * Fragility * The child has severe and/or life-threatening condition * Lack of availability and/or failure of equipment/technology or treatment places the child at immediate risk resulting in a negative health outcome * Short-term changes in the child's health status (e.g., an intercurrent illness) put them at immediate serious health risk * Chronicity * The child's condition is expected to last at least six more months * The child's life expectancy is less than six months * Complexity * Involvement of at least five healthcare practitioners/ teams and healthcare services are delivered in at least three of the following locations: Home, School/Nursing school, Hospital, Children's Treatment Centre, Community-based clinic (e.g. doctor's office), Other (at clinician's discretion)

Exclusion criteria

* High Utilization of hospital level care * ≥ 3 hospitalizations, ≥ 2 ICU admissions, ≥ 30 days of total hospitalization in previous 3 months, excluding newborn admission * Patient with tracheostomy and home ventilation * Medical Status is deemed highly fragile and the need for close follow-up is deemed essential by both referring and triaging team * Already followed by a complex care team * \>16.0 years of age * Inadequate English language skills to comprehend study questionnaires

Design outcomes

Primary

MeasureTime frameDescription
Service delivery outcomes: coordination of care among health providers and families, coordination of care between health providers and families, utility of follow-up planning toolsBaselineThese outcomes will be assessed with the Family Experiences with Coordination of Care (FECC) survey.

Secondary

MeasureTime frameDescription
Child physical painBaselineChildren's physical pain will be measured using only self or proxy reports of pain according to a 10 cm linear Visual Analog Scale (VAS).
Child quality of life & overall emotional healthBaselineThese outcomes will be assessed using the using the Feelings subscale from the KIDSCREEN-52 (6 items), used in over 250 studies in the child health services literature since its publication in 2005.
Parents' Perceived Emotional and Physical HealthBaselineParents' perceived health, energy, and fatigue will be assessed with short forms of the Patient Reported Outcomes Measurement Information System (PROMIS).
Effects of Child's Condition on Parents' Finances and Ability to WorkBaselineFinancial Impact on Parents' will be measured using an Expense Diary survey created by the co-investigators.
Parents' Quality of LifeBaselineParents' quality of life will be measured according to a subjective life appraisal definition with Diener's highly validated Satisfaction with Life Scale (SWLS) (5 items) which is the most validated life satisfaction scale in health and social sciences literature.

Other

MeasureTime frameDescription
Health systems outcomesBaselineThe investigators will link the patient-reported evaluation of the CCKO initiative with encoded health administrative data housed at ICES for consenting participants.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026