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Completed

NCT Number: NCT00853801

Integrating Lifestyle Therapy for Diabetes Prevention Into Primary Care

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

John H Stroger Hospital

Chicago, Illinois, 60612, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Lifestyle intervention and provider feedback

Behavioral

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.

Primary outcomes

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

    Time frame: 1.5 years

    Weight loss from baseline

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

    Time frame: 1.5 years

    Providers chart MetSyn in Problem List

Secondary outcomes

  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.

    Time frame: 1.5 years

    Patient verbalizes values leading to MetSyn diagnosis

  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.

    Time frame: 1.5 years

    Multidisciplinary team created

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

    Time frame: 1.5 years

    Database developed

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

    Time frame: 1.5 years

    Documentation

  5. Involve nursing staff in waist circumference measurement along with vital signs.

    Time frame: 1.5 years

    Waist measurements documented

  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.

    Time frame: 1.5 years

    HOMA-IR calculated

Sponsors and collaborators

Lead sponsor

Cook County Health

Other Gov

Registry information

Official study title

Detecting and Managing Metabolic Syndrome and Pre-Diabetes in General Medicine Clinic (Feasibility)

Important dates

Study start
2006
Primary completion
2007
Study completion
2010
First posted
Mar 2, 2009
Registry last updated
Jun 26, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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