Evaluation of the Transitional and Lifelong Care Program

Sponsor
Western University, Canada (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05849285
Collaborator
(none)
410
53

Study Details

Study Description

Brief Summary

The population cared for in the Transitional and Lifelong Care (TLC) clinic is youth and adults with childhood-onset disability, of which the large majority are adults with brain-based, neurodevelopmental conditions such as cerebral palsy, spina bifida and developmental disability. The TLC program was created to address the health inequities that have long existed for this population because of the gaps in care they experience once they transition from pediatric healthcare services to the adult healthcare sector. The TLC program offers coordinated and comprehensive management of co-occurring mental, social and physical health conditions for this group of adults with neurodiverse conditions. The proposed study will provide much needed evaluation of the TLC model as an intervention to provide transitional and lifelong care that reduces the barriers experienced because of the undefined clinic path - potentially more appropriately referred to as a "cliff" by a Freeman et al., (2015) - for these individuals. With appropriate evidence of effectiveness, scaling of the TLC program to other Ontario Health regions and more widely across Canada would improve access healthcare providers who are knowledgeable and competent in the management of physical and mental health conditions for adults with neurodiverse conditions as well as service integration and coordination between social and health sectors. The TLC clinic was co-designed with adults with neurodiverse conditions and health care providers in 2014 and represents a significant and sustainable change in the way healthcare has been delivered for this population in the Ontario Health West region over the last 7 years. More than 750 people have accessed coordinated and comprehensive care from Physiatrists, a Nurse Practitioner, Social Worker, Physiotherapist, Occupational Therapist, Speech Language Pathologist, Registered Dietitian and Rehabilitation Therapist in the TLC program since it began, documenting the effectiveness of this care has the power to re-shape care received for adults with neurodiverse conditions that onset in childhood in Canada.

Condition or Disease Intervention/Treatment Phase
  • Other: TLC Clinic

Study Design

Study Type:
Observational
Anticipated Enrollment :
410 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Evaluating a Model of Transitional and Lifelong Care for Adults With Childhood-Onset Disabilities
Anticipated Study Start Date :
Jul 1, 2023
Anticipated Primary Completion Date :
Dec 1, 2025
Anticipated Study Completion Date :
Dec 1, 2027

Arms and Interventions

Arm Intervention/Treatment
TLC Patient

Patients of the TLC program with CP/SB/DD

Other: TLC Clinic
Patients of the TLC clinic - receive coordinated multidisciplinary and specialized care from a team

Control Patient

Adults with CP/SB/DD that are not patients of the TLC Program

TLC Caregiver

Caregiver of Patients of the TLC program with CP/SB/DD

Other: TLC Clinic
Patients of the TLC clinic - receive coordinated multidisciplinary and specialized care from a team

Control Caregiver

Caregiver of Adults with CP/SB/DD that are not patients of the TLC Program

Healthcare Providers

Healthcare Providers who care for patients in the TLC clinic

Other: TLC Clinic
Patients of the TLC clinic - receive coordinated multidisciplinary and specialized care from a team

Outcome Measures

Primary Outcome Measures

  1. Patient Satisfaction [Year 1]

    MPOC-A

Secondary Outcome Measures

  1. Health Related Quality of Life [Year 1]

    EQ5D5L

  2. Health Related Quality of Life [Year 1]

    WHOQOL-BREF

  3. Caregiver Burden [Year 1]

    BSFC

  4. Perceived Support of Healthcare Providers [Year 1]

    MPOC-SP

  5. Economic Analysis [Year 2]

    Unit Costs of healthcare used

Eligibility Criteria

Criteria

Ages Eligible for Study:
21 Years and Older
Sexes Eligible for Study:
All
Inclusion Criteria:

Each participant dyad will consist of one person, of either sex and gender, who is over the age of 21 years with a childhood-onset disability, and the primary caregiver (based on contact hours) or support person, of either sex and gender, involved in their care. In cases where the patient participant is independent with care, a spouse or family member may still participate in the caregiver portion of the study.

  1. Patient participants will have continuously resided in Ontario during the years of 2015 to 2020 to facilitate full data retrieval from the administrative dataset.

  2. Healthcare providers, of any discipline, who provide care to adults with childhood-onset conditions in the TLC program.

Exclusion Criteria:

Patient participants will be ineligible if they are in a phase of deterioration associated with a progressive health condition identified either personally or by the caregiver participant.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Western University, Canada

Investigators

  • Principal Investigator: Laura K Brunton, PhD, Western University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Laura Brunton, Assistant Professor, Western University, Canada
ClinicalTrials.gov Identifier:
NCT05849285
Other Study ID Numbers:
  • 122419
  • 184575
First Posted:
May 8, 2023
Last Update Posted:
May 8, 2023
Last Verified:
May 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 8, 2023