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Integrated Client Care Project Trial: Wound Care Evaluation

Not Applicable
Completed
Conditions
Wound
Interventions
Other: integrated client care group
Registration Number
NCT01573832
Lead Sponsor
Sunnybrook Health Sciences Centre
Brief Summary

This study will use a randomized control trial design to compare wound care clients who receive "integrated care" versus "usual care" in Community Care Access Centres (CCAC) in Ontario. Data will be collected by existing administrative databases and linked by the Institute for Clinical Evaluative Sciences (ICES). The researchers will analyze these databases and report findings.

Detailed Description

The researchers are interested in finding out whether the intervention ("integrated care") helps to improve patient outcomes. A randomized control trial of wound care clients in Ontario CCACs will show the effects of the intervention (integrated care) versus "usual care" clients. The researchers will also examine the financial system costs associated with providing "integrated care" to clients versus "usual care".

The researchers expect to answer the research question of whether there is difference in patient outcomes between "integrated care" versus "usual care clients." The researchers also would like to formulate a response for whether there will be financial system cost difference between "integrated care" and "usual care" clients.

The goal of this evaluation is to help decision-makers in the Ministry of Health and Long Term Care (MOHLTC), in the Community Care Access Centres (CCACs) and among provider organizations to improve the quality of care and patient outcomes for wound care clients, by evaluating innovations in the delivery of care.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
13999
Inclusion Criteria
  • receives wound care from Community Care Access Centre provider
  • adults over age 18 in Ontario
Exclusion Criteria
  • patients who do not receive wound care from Ontario Community Care Access Centres

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Diabetic Foot Ulcer Interventionintegrated client care group-
Pionidal Sinus Ulcer Interventionintegrated client care group-
Primary Outcome Measures
NameTimeMethod
percentage of patients whose wound heals within the outcomes benchmark1 year

percentage of patients whose wound heals within the outcomes benchmark

Secondary Outcome Measures
NameTimeMethod
time to wound healing outcomes1 year

time to wound healing outcomes

total patient length of stayat patient discharge, up to 365 days

total patient length of stay

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