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Improving Diabetes Care Via Telephone Assessment and Patient Education

This study has been completed.
Study NCT00012649.   Last updated on October 31, 2008.   Information provided by Department of Veterans Affairs

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Descriptive Information Fields
Brief Title  Improving Diabetes Care Via Telephone Assessment and Patient Education
Official Title  Improving Diabetes Care Via Telephone Assessment and Patient Education
Brief Summary

The purpose of this study is to improve the quality of VA diabetes care using an automated telephone disease management (ATDM) system that administers patient assessments and targeted self-care education between clinic visits.

Detailed Description

Background:

The purpose of this study is to improve the quality of VA diabetes care using an automated telephone disease management (ATDM) system that administers patient assessments and targeted self-care education between clinic visits.

Objectives:

In this ongoing study, we are determining: 1) the reliability and validity of Automated Telephone Disease Management (ATDM) assessments of patients' glycemic control, health-related quality of life (HRQL), self-care, and satisfaction with care; 2) the extent to which these assessments identify patients at risk for poor outcomes; and 3) the cost-effectiveness of an intervention in which ATDM assessment reports are provided regularly to patients' primary care providers.

Methods:

We are refining and expanding previously-developed ATDM assessment instruments by incorporating measures of patient-centered outcomes. We are enrolling 450 patients from VISN 12 and VISN 21. Patients receive weekly ATDM assessments for six months. Other data on their health status and service use are being collected from medical records, laboratory tests, telephone surveys, and Austin Automation Center files. After determining the concurrent reliability, validity, and prognostic significance of the ATDM assessments, we will examine variation in ATDM-reported outcomes across Networks, facilities, and patient groups. In the second phase of the study, we will conduct an effectiveness trial with a one year follow up period. We will use the findings from our process evaluation to modify the ATDM assessments and design provider feedback reports. We will enroll 240 patients from the two Networks (i.e., 480 patients overall). Patients will be assigned to experimental or usual care control groups using a combination of randomization and cutoff-based assignment. We will measure the intervention's impact on patients' glycemic control, symptoms, self-care, and patient-centered outcomes. We will use VA costing database and Medicare claims files to evaluate cost-effectiveness.

Status:

Analyses of ATDM assessment data suggest that this method is feasible with VA diabetes patients and provides comparable data regarding patients' satisfaction with care and functioning to telephone surveys. Other analysis suggest that VA interpersonal processes of care and rates of cost-related medication adherence problems are as good or better than that experienced by patients with comparable characteristics treated in other systems of care.

Study Phase
Study Type  Observational
Study Design  Other
Primary Outcome Measure 
Secondary Outcome Measure 
Condition  Diabetes
Intervention 
MEDLINE PMIDs 12523921,   15144912,   15005508,   14747218,   14734946,   12643135,   12911644,   15364667,   15451750,   15208846,   16288094
Links
Recruitment Information Fields
Recruitment Status  Completed
Enrollment  0
Start Date 
Completion Date May 2003
Eligibility Criteria 

Inclusion Criteria:

Patients enrolled in VISN 12 and VISN 21

Exclusion Criteria:

Gender Both
Ages
Accepts Healthy Volunteers No
Contacts ††
Location Countries  United States
Administrative Information Fields
NCT ID  NCT00012649
Organization ID DII 99-187
Secondary IDs ††
Study Sponsor  Department of Veterans Affairs
Collaborators ††
Investigators 
Principal Investigator:     John D. Piette, PhD     VA Ann Arbor Healthcare System    
Information Provided By Department of Veterans Affairs
Verification Date January 2005
First Received Date  March 14, 2001
Last Updated Date October 31, 2008

 †    Required WHO trial registration data element.
††   WHO trial registration data element that is required only if it exists.




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