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Clinical Trials/NCT00302055
NCT00302055
Completed
Not Applicable

Feasibility of a Partnered Approach to Prevent Diabetes

Northwestern University2 sites in 1 country72 target enrollmentMarch 2006

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pre-diabetic State
Sponsor
Northwestern University
Enrollment
72
Locations
2
Primary Endpoint
Weight Loss
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The Diabetes Prevention Program (DPP) demonstrated that an intensive lifestyle intervention resulting in modest weight loss and increased physical activity can delay or prevent the development of type 2 diabetes in those at increase risk for the disease. The lifestyle program used, however, was not designed for delivery on a public health scale. Successful DPP translation will require a sustainable partnership between a health care system and an established community organization committed to community health and experienced in implementing sustainable health and wellness programs. We have been collaborating with local health system and community administrators for over a year to design a 'real-world' clinic-based screening model to identify and refer high-risk patients for a group-based adaptation of the DPP lifestyle intervention in community facilities. We have designed this study to develop preliminary data about the feasibility and yield of clinic-based screening and referral, as well as the effectiveness of the adapted lifestyle intervention. This pilot study seeks to: 1) evaluate the feasibility of a strategy to implement American Diabetes Association (ADA) recommendations for clinic-based diabetes-risk testing and to refer high-risk patients for a community-based lifestyle intervention; 2) compare two strategies to enhance community-based program participation by referred patients; 3) demonstrate the capability of community facilities to schedule and enroll referred clinic patients at high-risk for diabetes and to deliver a modified, group-based DPP lifestyle intervention consistently; and 4) compare levels of weight loss and physical activity achieved by referred clinic patients with pre-diabetes who participate in a free-of-charge, group-based DPP lifestyle intervention at community facilities compared to a free-of-charge, traditional, one-on-one DPP lifestyle intervention at a DPP research site. Addressing these issues now will enable us to evaluate this partnered DPP translation model with a larger, more robust future study that will involve referral by multiple primary care clinics, program delivery at more community sites, and a 3-year follow-up period.

Registry
clinicaltrials.gov
Start Date
March 2006
End Date
July 2007
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ronald Ackermann

Professor

Northwestern University

Eligibility Criteria

Inclusion Criteria

  • 25 years of age or older Body-mass index of \>= 24 kg/m2
  • or more additional risk factors if age is \<45
  • Parent or sibling with diabetes
  • Minority race or ethnicity
  • History of gestational diabetes
  • Delivery of infant \>= 9 lbs.
  • History of high blood pressure
  • History of dyslipidemia
  • Polycystic Ovarian Syndrome
  • History of vascular disease Fasting Capillary Glucose 95 - 125 mg/dl 2-hour Post-challenge Capillary Glucose 140 - 199 mg/dl

Exclusion Criteria

  • Diseases that could limit lifespan or increase risk with a lifestyle intervention - Cancer diagnosed in the past 5 years
  • Significant Cardiovascular Disease
  • A "Yes" response to any item on the modified Physical Activity Readiness Questionnaire
  • Uncontrolled hypertension: systolic blood pressure \>180 mmHg or diastolic blood pressure \>105 mmHg
  • Heart attack, stroke, or transient ischemic attack within 6 months
  • Chest pain or unexplained dizziness or fainting with physical exertion
  • Chronic obstructive pulmonary disease or asthma needing home oxygen
  • Other chronic disease or condition, such as advanced arthritis, that could limit ability to become physically active or limit life span to \<5 years
  • Any other known reason for not participating in regular physical activity
  • Exclusions related to metabolism - Past anti-diabetes medication use, except during gestational diabetes

Outcomes

Primary Outcomes

Weight Loss

Time Frame: 12 months

We analyzed repeated outcome measures using longitudinal linear regression with 3 observations per participant (baseline, 6 months, and 12 months)

Secondary Outcomes

  • Self Report Physical Activity(12 months)
  • Rate of Community Program Participation(6 months)

Study Sites (2)

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