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Completed

NCT Number: NCT02928757

Complex Care for Kids Ontario (CCKO)

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.

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Key information

Conditions

Children with Medical Complexity

Age range

0 year–16 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hamilton Health Sciences, Hamilton, Ontario, Canada

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Complex care clinic as part of the CCKO initiative

Other

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.

Primary outcomes

  1. Service delivery outcomes: coordination of care among health providers and families, coordination of care between health providers and families, utility of follow-up planning tools

    Time frame: Baseline

    These outcomes will be assessed with the Family Experiences with Coordination of Care (FECC) survey.

  2. Service delivery outcomes: coordination of care among health providers and families, coordination of care between health providers and families, utility of follow-up planning tools

    Time frame: 6 months

    These outcomes will be assessed with the Family Experiences with Coordination of Care (FECC) survey.

  3. Service delivery outcomes: coordination of care among health providers and families, coordination of care between health providers and families, utility of follow-up planning tools

    Time frame: 12 months

    These outcomes will be assessed with the Family Experiences with Coordination of Care (FECC) survey.

  4. Service delivery outcomes: coordination of care among health providers and families, coordination of care between health providers and families, utility of follow-up planning tools

    Time frame: 24 months

    These outcomes will be assessed with the Family Experiences with Coordination of Care (FECC) survey.

Secondary outcomes

  1. Child quality of life & overall emotional health

    Time frame: Baseline

    These 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.

  2. Child quality of life & overall emotional health

    Time frame: 6 months

    These 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.

  3. Child quality of life & overall emotional health

    Time frame: 12 months

    These 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.

  4. Child quality of life & overall emotional health

    Time frame: 24 months

    These 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.

  5. Child physical pain

    Time frame: Baseline

    Children's physical pain will be measured using only self or proxy reports of pain according to a 10 cm linear Visual Analog Scale (VAS).

  6. Child physical pain

    Time frame: 6 months

    Children's physical pain will be measured using only self or proxy reports of pain according to a 10 cm linear Visual Analog Scale (VAS).

  7. Child physical pain

    Time frame: 12 months

    Children's physical pain will be measured using only self or proxy reports of pain according to a 10 cm linear Visual Analog Scale (VAS).

  8. Child physical pain

    Time frame: 24 months

    Children's physical pain will be measured using only self or proxy reports of pain according to a 10 cm linear Visual Analog Scale (VAS).

  9. Parents' Quality of Life

    Time frame: Baseline

    Parents' 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.

  10. Parents' Quality of Life

    Time frame: Baseline

    Parents' quality of life will also be measured with an adapted version of the KIDSCREEN survey subscale for Feelings.

  11. Parents' Quality of Life

    Time frame: 6 months

    Parents' 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.

  12. Parents' Quality of Life

    Time frame: 6 months

    Parents' quality of life will also be measured with an adapted version of the KIDSCREEN survey subscale for Feelings.

  13. Parents' Quality of Life

    Time frame: 12 months

    Parents' 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.

  14. Parents' Quality of Life

    Time frame: 24 months

    Parents' 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.

  15. Parents' Quality of Life

    Time frame: 12 months

    Parents' quality of life will also be measured with an adapted version of the KIDSCREEN survey subscale for Feelings.

  16. Parents' Quality of Life

    Time frame: 24 months

    Parents' quality of life will also be measured with an adapted version of the KIDSCREEN survey subscale for Feelings.

  17. Parents' Perceived Emotional and Physical Health

    Time frame: Baseline

    Parents' perceived health, energy, and fatigue will be assessed with short forms of the Patient Reported Outcomes Measurement Information System (PROMIS).

  18. Parents' Perceived Emotional and Physical Health

    Time frame: 6 months

    Parents' perceived health, energy, and fatigue will be assessed with short forms of the Patient Reported Outcomes Measurement Information System (PROMIS).

  19. Parents' Perceived Emotional and Physical Health

    Time frame: 12 months

    Parents' perceived health, energy, and fatigue will be assessed with short forms of the Patient Reported Outcomes Measurement Information System (PROMIS).

  20. Parents' Perceived Emotional and Physical Health

    Time frame: 24 months

    Parents' perceived health, energy, and fatigue will be assessed with short forms of the Patient Reported Outcomes Measurement Information System (PROMIS).

  21. Effects of Child's Condition on Parents' Finances and Ability to Work

    Time frame: Baseline

    Financial Impact on Parents' will be measured using an Expense Diary survey created by the co-investigators.

  22. Effects of Child's Condition on Parents' Finances and Ability to Work

    Time frame: 6 months

    Financial Impact on Parents' will be measured using an Expense Diary survey created by the co-investigators.

  23. Effects of Child's Condition on Parents' Finances and Ability to Work

    Time frame: 12 months

    Financial Impact on Parents' will be measured using an Expense Diary survey created by the co-investigators.

  24. Effects of Child's Condition on Parents' Finances and Ability to Work

    Time frame: 24 months

    Financial Impact on Parents' will be measured using an Expense Diary survey created by the co-investigators.

Other outcomes

  1. Health systems outcomes

    Time frame: Baseline

    The investigators will link the patient-reported evaluation of the CCKO initiative with encoded health administrative data housed at ICES for consenting participants.

  2. Health systems outcomes

    Time frame: 6 months

    The investigators will link the patient-reported evaluation of the CCKO initiative with encoded health administrative data housed at ICES for consenting participants.

  3. Health systems outcomes

    Time frame: 12 months

    The investigators will link the patient-reported evaluation of the CCKO initiative with encoded health administrative data housed at ICES for consenting participants.

  4. Health systems outcomes

    Time frame: 24 months

    The investigators will link the patient-reported evaluation of the CCKO initiative with encoded health administrative data housed at ICES for consenting participants.

Sponsors and collaborators

Lead sponsor

The Hospital for Sick Children

Other

Collaborators

  • Children's Hospital of Eastern Ontario
  • Hamilton Health Sciences Corporation
  • London Health Sciences Centre

Registry information

Official study title

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

Important dates

Study start
2016
Primary completion
2021
Study completion
2021
First posted
Oct 10, 2016
Registry last updated
Sep 8, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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