Community-based Personalized Care and QOL
- Conditions
- AgingDisability or Chronic Disease Leading to Disablement
- Interventions
- Behavioral: Community-based personalized care
- Registration Number
- NCT03263169
- Lead Sponsor
- Windsor-Essex Compassionate Care Community
- Brief Summary
A pragmatic randomized trial to evaluate the impact of an integrated patient experience and outcome measurement system supported by citizens, caregivers and community through eHealth technology.
The primary research question is: What is the effectiveness of the WECCC approach on quality of life in people aged 65 and older or who self-identify as disabled compared to people not receiving the Health TAPESTRY program?
- Detailed Description
Secondary research questions include:
1. what is the feasibility of obtaining study measures through routinely collected program participant data and what design adjustments are needed to balance pragmatism and high quality data collection?
2. What are the analytic approaches to be developed to aggregate data from individual participants into meaningful units (e.g. care-team level, organizational level, social network, and geographic area) to inform ongoing adaptation of the components of the intervention?
3. what are the perceptions of knowledge users on the usefulness of comparative effectiveness pragmatic trial evidence?
The project involves using administrative data from the ICES to create outcome measures and feedback systems for communities, and the INSPIRE PHC Unit for expertise in health system integration, care in the community, and knowledge translation.
Inclusion criteria: Seniors (65+) and people who self-identify as having a functional disability. Pilot study sites: 7 municipalities and the city of Windsor in Windsor-Essex County in Ontario. The combined total eligible population in all 8 sites is about 60,000 people, from which a minimum sample of 3000 registered patients and 1000 registered caregivers will be drawn
In Year 1, planned enrolment includes a minimum of 1100 intervention clients from all recruitment methods in the care model intervention, with similar numbers of control and intention to treat clients.
The primary outcomes are quality of life (QOL); perceived health; experience of care, and perceived social connection.
The primary outcomes for caregivers will be quality of life; perceived burden; caregiver perceptions of care; and perceived social connection.
Secondary outcomes for both will include goal attainment, distress management, symptom management, places of care, and health care utilization and costs. In terms of health equity, the investigators will measure the difference between the average/median population quality of life and cost outcomes compared to patients at the bottom income quartiles stratified by risk level. At a systems level, algorithms will be developed and applied to the data collected from participants to provide aggregate organization and system-level reports, co-designed with end users to support them as learning organizations.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 1100
Individuals who:
- are 65 years of age and over
- have a long-term disability or one or more chronic diseases
- able to communicate in English OR can provide a formal or informal translator willing to facilitate the participant's involvement
Individuals not meeting above criteria
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description WE Health Tapestry Community-based personalized care Completion of baseline measures then enrolled in a community-based personalized care intervention that consists of four core elements: volunteer support, interprofessional care, technology, social network linkage Usual Care Community-based personalized care Completion of baseline measures with six-month delayed community-based personalized care intervention: volunteer support, interprofessional care, technology, social network linkage
- Primary Outcome Measures
Name Time Method Quality of Life Baseline and then monthly for 24 months McGill QoL - patient and family
Perceived health Baseline and then monthly for 24 months EQ-5D-5L - patient
- Secondary Outcome Measures
Name Time Method Patient experience Baseline and then monthly for 24 months CANHelp Patient
Health services utilization 1 Baseline and then monthly for 24 months hospitalization
Symptom management 1 Baseline and then monthly for 24 months Edmonton Symptom Assessment Scale
Symptom management 2 Baseline and then monthly for 24 months Palliative Performance Scale
Caregiver Burden 2 Baseline and then monthly for 24 months Zarit burden interview
Symptom management 3 Baseline and then monthly for 24 months InterRAI-home care
Health services utilization 2 Baseline and then monthly for 24 months Emergency care
Caregiver Burden 1 Baseline and then monthly for 24 months InterRAI-home care
Family experience Baseline and then monthly for 24 months CANHelp Family
Trial Locations
- Locations (1)
Windsor-Essex Compassionate Care Community Program Management Office
🇨🇦Windsor, Ontario, Canada