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Clinical Trials/NCT03075709
NCT03075709UnknownNot Applicable

The Development, Implementation and Evaluation of Clinical Pathways for Chronic Obstructive Pulmonary Disease (COPD) in Saskatchewan

University of Saskatchewan1 site in 1 country800 target enrollmentStarted: September 30, 2017Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
800
Locations
1
Primary Endpoint
Quality of Care

Study Overview

Brief Summary

Chronic obstructive pulmonary disease (COPD) has substantial economic and human costs. To minimize these costs high quality guidelines have been developed. However, development of guidelines alone rarely results in changes to practice. One method of integrating guidelines into professional practice is the use of clinical pathways (CPWs).

The investigators are working with local stakeholders to develop CPWs for COPD with the aims of improving quality of care and guideline adherence while reducing healthcare utilization. The CPWs will utilize several steps including: standardizing diagnostic training, implementing and unifying common components of chronic disease care, coordinating the provision of education and reconditioning programs, and ensuring disease specific care utilizes and delivers evidence-informed practices. In addition, the investigators have worked to identify evidence-informed strategies for the implementation of the CPWs. Efforts are underway to tailor these implementation strategies for the local context.

The investigators will conduct a three-year quantitative health services research project using an interrupted time series (ITS) design in the form of a multiple baseline approach with control groups. The CPW will be implemented in two Saskatchewan health regions (experimental groups) and two health regions will act as controls (control groups). The experimental and control groups will each contain one urban and one rural health region.

This project is expected to improve quality of life and reduce healthcare utilization. The project will also provide evidence on the effects of CPWs in both urban and rural settings. If the pathways are found effective the investigators will work with all stakeholders to implement similar CPWs for the remaining health regions in the province.

Study Design

Study Type
Observational
Observational Model
Other
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • All individuals with diagnosed chronic obstructive pulmonary disease (COPD)

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Quality of Care

Time Frame: 36 months

Operationalized as hospital readmission rates and and emergency department (ED) presentation rates

Secondary Outcomes

  • Healthcare Utilization(36 months)
  • Guideline Adherence(36 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Thomas Rotter

Research Chair in Health Quality Improvement Science

University of Saskatchewan

Study Sites (1)

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