Viewing Study NCT00384488



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Study NCT ID: NCT00384488
Status: COMPLETED
Last Update Posted: 2006-10-06
First Post: 2006-10-05

Brief Title: Automated Diabetes Prevention Program
Sponsor: Kaiser Permanente
Organization: Kaiser Permanente

Study Overview

Official Title: Effectiveness of Automated Telephone Intervention on Behavioral and Weight Outcomes for Patients With Pre-Diabetes
Status: COMPLETED
Status Verified Date: 2006-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
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

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None