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Clinical Trials/NCT00906919
NCT00906919
Completed
Not Applicable

The Effectiveness of Diabetes Patient Education and Self-Management Education in Persons With Type 2 Diabetes

University of Victoria1 site in 1 country321 target enrollmentApril 2004

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Diabetes Mellitus, Type 2
Sponsor
University of Victoria
Enrollment
321
Locations
1
Primary Endpoint
A1C
Status
Completed
Last Updated
16 years ago

Overview

Brief Summary

The goal of this randomized controlled trial is to determine if greater effectiveness can be achieved by the addition of lay-led self-management patient education to regular professionally-led diabetes patient education in comparison to regular professionally-led diabetes patient education only.

Detailed Description

In the current health care environment, it is unacceptable for patient education programs to merely provide information. Rather, educational programs must concentrate on behavior change and on supporting patients to become more confident and motivated in participating in managing their health. Persons with type 2 diabetes attending a Diabetes Education Centre will be assigned to either a group that receives regular professionally-led diabetes patient education (control group) or to to a group that receives regular professionally-led diabetes patient education augmented by lay-led self-management education i.e., the Stanford six-session Chronic Disease Self-Management Program (experimental group). Data will be collected at two points in time (0 and 6 months). Outcome measures will show if participants who receive self-management training in addition to regular patient education are able to:manage their diabetes more effectively; engage in the specific behaviors that keep the condition from worsening; achieve more control over their condition; and use the health care system more effectively.

Registry
clinicaltrials.gov
Start Date
April 2004
End Date
April 2009
Last Updated
16 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • adults with type 2 diabetes

Exclusion Criteria

  • cognitive impairment
  • unable to speak English

Outcomes

Primary Outcomes

A1C

Time Frame: 6 months

Secondary Outcomes

  • Self-management behaviors(6 months)
  • Self-efficacy levels(6 months)
  • Health status(6 months)
  • Cholesterol levels(6 months)

Study Sites (1)

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