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Clinical Trials/NCT00384488
NCT00384488
Completed
Not Applicable

Effectiveness of Automated Telephone Intervention on Behavioral and Weight Outcomes for Patients With Pre-Diabetes.

Kaiser Permanente1 site in 1 country84 target enrollmentMay 2004
ConditionsPre-Diabetes

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pre-Diabetes
Sponsor
Kaiser Permanente
Enrollment
84
Locations
1
Primary Endpoint
Weight loss
Status
Completed
Last Updated
19 years ago

Overview

Brief Summary

The objective for this pilot project is to determine the feasibility and effectiveness of the Interactive Voice Response protocol (IVR) on physical activity and eating behaviors in a group men and women who have been identified by their physician as being pre-diabetic. We hypothesize that participants receiving the IVR follow-up will have greater positive changes in their physical activity and eating behaviors when compared to those who receive only the standard-care pre-diabetes class.

Detailed Description

Patients diagnosed with pre-diabetes present a unique opportunity for health care providers to implement preventive practices. Behavioral intervention strategies that target weight reduction or maintenance and increased fitness not only provide exceptional cardiovascular benefits, but also play an important role in delayed development or prevention of type 2 diabetes mellitus (DM). This study was designed to determine the feasibility and effectiveness of automated telephone support calls targeting physical activity and healthful eating as strategies for weight loss for patients with pre-diabetes. Participants with pre-diabetes who participated in a 90-minute diabetes prevention class were consented to participate in this behavioral study and were then randomly assigned to receive automated telephone support targeting physical activity and nutrition weight loss strategies or to a no-contact control group. Objective physical activity (accelerometer), self-reported dietary intake, and body weight were assessed at baseline and at 3-months follow-up.

Registry
clinicaltrials.gov
Start Date
May 2004
End Date
May 2006
Last Updated
19 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Male and female Kaiser-Permanente of Colorado members age 18 and above who have been diagnosed with pre-diabetes and who have enrolled in a clinically indicated pre-diabetes class.
  • Subjects must be English speaking and have a telephone

Exclusion Criteria

  • Pregnant females
  • Enrollment in another research study involving diabetes or weight management during the time of the study.

Outcomes

Primary Outcomes

Weight loss

Secondary Outcomes

  • Increased physical activity
  • Improved healthy eating habits
  • Weight maintenance
  • Reduction in progression to type 2 DM

Study Sites (1)

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