Integrating Lifestyle Therapy for Diabetes Prevention Into Primary Care

Sponsor
John H. Stroger Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT00853801
Collaborator
(none)
112
1
1
58
1.9

Study Details

Study Description

Brief Summary

An educational intervention in the General Medicine Clinic aimed at both primary care providers (PCPs) and their patients with metabolic syndrome/pre-diabetes (MetSyn/PDM). Improving PCPs ability to detect and manage MetSyn/PDM, as measured by the increased incorporation of MetSyn/PDM into PCPs care plan, and increasing patients' awareness of healthy lifestyle behaviors results in positive patient health behaviors and outcomes.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Lifestyle intervention and provider feedback
N/A

Detailed Description

The highest diabetes prevalence in the US is among African Americans (13.3%), American Indians (12.8%), and Mexican Americans (9.5%) with 8.7% of European Americans diagnosed with diabetes. In addition, certain minorities also have much higher rates of diabetes-related complications and death, in some instances by as much as 50% more than the general population, highlighting that the greatest need for preventive measures are amongst ethnic minorities.

The efficacy of lifestyle intervention in reducing the incidence of type 2 diabetes has been established by the Diabetes Prevention Program and other studies. The Cook County Bureau of Health Services, a publicly-funded healthcare system serving a primarily low-income, uninsured, ethnically diverse population in Chicago, IL, currently treats an estimated 40,000 patients annually for type 2 diabetes and estimates that another 85,000 to 100,000 patients are at risk for developing diabetes.

Our primary objective was to test the feasibility of integrating less intensive lifestyle intervention therapy into patient visits with their primary care provider to improve weight loss and decrease the intensity of metabolic syndrome and pre-diabetes risk factors. The site of the study is the General Medicine Clinic, a busy primary care outpatient site treating approximately 12,000 patients/year and 200 patients/day, staffed primarily by medical residents supervised by attending physicians.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
112 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Care Provider)
Primary Purpose:
Prevention
Official Title:
Detecting and Managing Metabolic Syndrome and Pre-Diabetes in General Medicine Clinic (Feasibility)
Study Start Date :
Feb 1, 2006
Actual Primary Completion Date :
Nov 1, 2007
Actual Study Completion Date :
Dec 1, 2010

Arms and Interventions

Arm Intervention/Treatment
Experimental: 1

Lifestyle modification education and counseling for intervention patients. Diagnosis and treatment education and feedback on performance for providers of intervention patients.

Behavioral: Lifestyle intervention and provider feedback
Patients receive lifestyle education and counseling after each visit with their primary care provider. Lifestyle modification goals are set and progress monitored. Frequency is dependent on frequency of visits with primary care provider which can range from one month to nine months. Primary care providers of the intervention patients receive one education session at the commencement of the study covering the diagnosis and treatment of metabolic syndrome and pre-diabetes. Feedback on provider performance as assessed by provider documentation of diagnosis and treatment recommendations compared to patient outcomes is given every six months.

Outcome Measures

Primary Outcome Measures

  1. Patients adopt healthy lifestyle behaviors leading to significant weight loss, thus reducing their risk of diabetes and heart disease [1.5 years]

  2. Providers improve their ability to diagnose and treat metabolic syndrome/pre-diabetes. [1.5 years]

Secondary Outcome Measures

  1. Improve patient understanding of the metabolic syndrome/pre-diabetes risk parameters and the impact of healthy lifestyle changes on reducing their risk of developing heart disease and diabetes. [1.5 years]

  2. Create a model multidisciplinary team (physician, nurse, dietitian, health educator) to conduct group visits, lifestyle intervention education and follow-up of patients with metabolic syndrome/pre-diabetes. [1.5 years]

  3. Develop a system-wide database of patients with metabolic syndrome/pre-diabetes to target for preventive care. [1.5 years]

  4. Establish physician discussions and documentations encouraging lifestyle changes such as weight loss, healthy dietary changes and exercise. [1.5 years]

  5. Involve nursing staff in waist circumference measurement along with vital signs. [1.5 years]

  6. Assess changes in insulin resistance using the HOMA-IR index and in vascular inflammation status using C-Reactive protein in the intervention and control groups. [1.5 years]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Has metabolic syndrome as defined by three or more of the five risk factors:

  • elevated blood pressure (BP) above 130 mm Hg systolic and/or 85 mm Hg diastolic or drug therapy for elevated blood pressure

  • elevated waist circumference (WC)above 35" (female) or above 40" (male)

  • reduced high-density lipoprotein (HDL) of below 40 mg/dl (male) or below 50 mg/dl (female) or drug therapy for reduced HDL

  • elevated triglycerides (TG) of 150 mg/dl or above or drug therapy for elevated TG

  • elevated fasting blood glucose (FBG) of 100 mg/dl and above and below 126 mg/dl)or pre-diabetes as defined as elevated FBG.

  • Has a primary care provider in the General Medicine Clinic (GMC).

Exclusion Criteria:
  • Has been diagnosed with any of the following:

  • diabetes

  • known CAD (MI, CABG, PTCA)

  • congestive Heart Failure NYHA Class III or IV

  • Life expectancy less than 2 years

  • Non-English speaking patient

  • Patient whose physician is a PGY-3 resident, graduating before projected completion of the study

Contacts and Locations

Locations

Site City State Country Postal Code
1 John H Stroger Hospital Chicago Illinois United States 60612

Sponsors and Collaborators

  • John H. Stroger Hospital

Investigators

  • Principal Investigator: Leon Fogelfeld, MD, John H. Stroger Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Leon Fogelfeld, Chair, Division of Endocrinology, John H. Stroger Hospital
ClinicalTrials.gov Identifier:
NCT00853801
Other Study ID Numbers:
  • MetSyn-PDM
First Posted:
Mar 2, 2009
Last Update Posted:
Oct 2, 2014
Last Verified:
Sep 1, 2014

Study Results

No Results Posted as of Oct 2, 2014