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Clinical Trials/NCT00414986
NCT00414986CompletedNot Applicable

Using Learning Teams for Reflective Adaptation

University of Colorado, Denver1 site in 1 country1,565 target enrollmentStarted: September 1, 2005Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
1,565
Locations
1
Primary Endpoint
Surveillance of Hemoglobin A1c, blood pressure, lipids, depression process of care

Study Overview

Brief Summary

The study will randomize 54 primary care practices to two intervention and a comparison groups. Both interventions will involve an on-site Improvement Facilitator who will assist the practice in forming an Improvement Team, using rapid-cycle tests of change, and implementing chronic care office systems for type 2 diabetes and depression. One intervention is based on complexity science and the other is a traditional QI intervention.

Detailed Description

Evidence-based guidelines for primary care of diabetes have been established and disseminated, yet adoption of guidelines in community-based primary care practice has been disappointing. This effectiveness study proposes a randomized trial involving 54 community-based primary care practices to test two innovative interventions to improve diabetes and depression care. One intervention, derived from theoretically based and efficacious programs tested in other settings, adopts a broad focus and seeks to improve diabetes and depression care by a) increasing the practice's organizational capacity to manage change, and b) implementing and sustaining chronic care office systems that support clinician efforts to improve care for diabetes. The intervention will combine two integrated components. The first component will utilize an Improvement Facilitator that will assess the practice's current use of chronic care office systems and their organizational capacity to manage change, provide feedback to key stakeholders in the practice, and work with the practice over six months to form an Improvement Team that will both address organizational capacity to create and sustain improvement and implement chronic care systems. In the second component of the intervention, the practice will participate in a local Improvement Collaborative that will afford opportunities to learn and share experiences during implementation and maintenance phases of the intervention with five similar practices in their geographic area. The second intervention is based on traditional QI methods and focuses on a chronic disease registry with regular reports to the physicians. It also uses PDSA cycles to assist in implementing change. This intervention will offer tools to improve diabetes and/or asthma care. Both interventions will be evaluated in two ways. First, a randomized trial using rigorous quantitative methods will measure 2 primary and 3 secondary endpoints at 9 and 18 months, including a) the ADA Physician Recognition Program performance measures by both patient-report and review of the medical record, and b) HEDIS measures of acute phase management of depression, c) assessment of the extent to which practices implement and physicians use elements of the chronic care model in their care of diabetes and depression. Change from baseline to 9 months will assess adoption of chronic care improvements, and change from 9 to 18 months will assess sustainability of improvements. Second, a multimethod assessment process will be used to analyze all qualitative and quantitative data separately to understand how and why the intervention led to the observed effects. The practice assessment will strive to understand which components of the interventions were most effective, their relative costs for implementation, and how they might be further improved. Successful components of the intervention will be refined and made available to our collaborators in the project; the Copic Insurance Company and the Colorado Clinical Guidelines Collaborative, for use in their statewide activities to improve diabetes care.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Single Group
Primary Purpose
Health Services Research
Masking
None

Eligibility Criteria

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

Inclusion Criteria

  • •Under primary care for type 2 diabetes

Exclusion Criteria

  • •Are not minimally literate in either English or Spanish

Arms & Interventions

1

Experimental

Practice in this arm will receive the Chronic Care Improvement intervention

Intervention: Chronic Care Improvement (CCI) Intervention (Behavioral)

2

Experimental

Practices in this arm will receive the standard CQI intervention. An in-practice CQI coordinator will assist the practices in implement a chronic disease registry.

Intervention: Standard CQI intervention (Behavioral)

3

Active Comparator

Practice in this arm will have access to all chronic care tools, but will not have an in-practice change agent.

Intervention: Self-directed practice comparison (Behavioral)

Outcomes

Primary Outcomes

Surveillance of Hemoglobin A1c, blood pressure, lipids, depression process of care

Time Frame: Baseline, 9, and 18 month

HEDIS-like measures of acute phase management of depression

Time Frame: Baseline, 9, and 18 months

Secondary Outcomes

  • Patient report (by survey) of their primary care experience(baseline, 9-months, 18-months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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