Diabetes Prevention Program Pilot Study

Diabetes Prevention Clinical Trial

— DPP  

Official title:

Virtual Translation of Diabetes Prevention to Primary Care: A Pilot Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00729079
• Other study ID #: 24895
• Status: Completed
• Phase: N/A
• First received: August 1, 2008
• Last updated: October 8, 2015
• Start date: December 2008
• Est. completion date: October 2009

Study information

• Verified date: March 2013
• Source: University of Rochester
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

This pilot study is intended to demonstrate that we can actually deliver the Diabetes Prevention Program intervention well and to show that it is likely effective. We will use results from this pilot study to support our application to The National Institute of Health. NIH is asking for health care centers to show ways to provide this treatment at a reasonable cost. We propose to demonstrate successful and sustainable use DPP's lifestyle intervention in a primary care health care setting (University of Rochester Primary Care).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 36
• Est. completion date: October 2009
• Est. primary completion date: July 2009
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 90 Years

Eligibility

Inclusion Criteria:

• Age >18 years

• BMI >24 kg/m2 (>22 kg/m2 among Asian Americans)

• IGT (2-h plasma glucose 140~199 mg/dl based on 75-g OGTT if available). The OGTT will not be required for inclusion, but the CMA practitioners may wish to recommend the OGTT for their patients.

• Elevated FPG (95~125 mg/dl*).

• HDL-triglyceride ration > 3.5.

Exclusion Criteria:

• Diabetes at baseline

• FPG >126 mg/dl*

• 2-h plasma glucose >200 mg/dl based on 75-g OGTT, if available. OGTT will not be required (see above note).

• Diabetes diagnosed by a physician and confirmed by other clinical data, other than during pregnancy.

• Ever used antidiabetic medication, other than during pregnancy

• Medical conditions likely to limit life span and/or increase risk of intervention

• Cardiovascular disease

• Hospitalization for treatment of heart disease in past 6 months New York Heart Association Functional Class> 2

• Left bundle branch block or third degree AV block Aortic stenosis

• Systolic blood pressure> 180 mmHg or diastolic blood pressure> 105 mmHg

• Cancer requiring treatment in the past 5 years, unless the prognosis is considered good

• Renal disease (creatinine GFR < or = 30 ml/hr or > 2.0 mg/dl if GFR not available).

• Anemia (hematocrit <36% in men or <33% in women)

• Hepatitis (based on history or serum transaminase elevation)

• Other gastrointestinal disease (pancreatitis, acute inflammatory bowel disease)

• Recent or significant abdominal surgery

• Pulmonary disease with dependence on oxygen or daily use of bronchodilators

• Chronic infection (e.g., HIV, active tuberculosis)

• Conditions or behaviors likely to affect conduct of the trial

• Unable to communicate with clinic staff (e.g., read and speak English).

• Unwilling to accept treatment assignment by randomization

• Participation in another intervention research project that might interfere with DPP

• Weight loss of > 10% in past 6 months for any reason except postpartum weight loss

• Unable to walk 0.25 miles in 10 min

• Currently pregnant or within 3 months postpartum

• Currently nursing or within 6 weeks of having completed nursing

• Pregnancy anticipated during the course of the trial

• Unwilling to undergo pregnancy testing or report possible pregnancy promptly

• Unwilling to take adequate contraceptive measures, if potentially fertile

• Major psychiatric disorder, including severe active major depression, severe anxiety, schizophrenia, manic depression, bi-polar disorder

• Excessive alcohol intake, either acute or chronic

• Medications and medical conditions likely to confound the assessment for diabetes including:

• Niacin, in doses indicated for lowering serum triglycerides

• Glucocorticoids, systemic

• Other prescription weight-loss medications

• Active Thyroid disease, suboptimally treated as indicated by abnormal serum thyroid-stimulating hormone

• Other endocrine disorders (e.g., Cushing's syndrome, acromegaly)

• Fasting plasma triglyceride >600 mg/dl, despite treatment

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

• Diabetes Mellitus
• Diabetes Prevention

Intervention

Behavioral:
• DPP
The primary outcome measure is weight loss with a goal of 7% of initial weight. Secondary outcomes are adherence to behavior changes: Exercising a minimum of 150 minutes per week at a moderate level to maintain an energy expenditure of 700 kcals per week Fat intake less than 25% and saturated fat less than 10% Fiber intake of at least 25 grams per day Fasting blood sugar < 100 mg/dL Absence of tobacco use
• DPP
The primary outcome measure is weight loss with a goal of 7% of initial weight. Secondary outcomes are adherence to behavior changes: Exercising a minimum of 150 minutes per week at a moderate level to maintain an energy expenditure of 700 kcals per week Fat intake less than 25% and saturated fat less than 10% Fiber intake of at least 25 grams per day Fasting blood sugar < 100 mg/dL Absence of tobacco use

Locations

Country	Name	City	State
United States	Clinton Medical Associated	Rochester	New York
United States	Therapeutic Lifestyle Changes	Rochester	New York

Sponsors (1)

Lead Sponsor	Collaborator
University of Rochester

Country where clinical trial is conducted

United States, 

References & Publications (8)

American Diabetes Association. Standards of medical care in diabetes--2008. Diabetes Care. 2008 Jan;31 Suppl 1:S12-54. doi: 10.2337/dc08-S012. — View Citation

Benjamin SM, Valdez R, Geiss LS, Rolka DB, Narayan KM. Estimated number of adults with prediabetes in the US in 2000: opportunities for prevention. Diabetes Care. 2003 Mar;26(3):645-9. — View Citation

Goldstein MG, Whitlock EP, DePue J; Planning Committee of the Addressing Multiple Behavioral Risk Factors in Primary Care Project. Multiple behavioral risk factor interventions in primary care. Summary of research evidence. Am J Prev Med. 2004 Aug;27(2 Suppl):61-79. Review. — View Citation

Herman WH, Hoerger TJ, Brandle M, Hicks K, Sorensen S, Zhang P, Hamman RF, Ackermann RT, Engelgau MM, Ratner RE; Diabetes Prevention Program Research Group. The cost-effectiveness of lifestyle modification or metformin in preventing type 2 diabetes in adults with impaired glucose tolerance. Ann Intern Med. 2005 Mar 1;142(5):323-32. — View Citation

Maciosek MV, Edwards NM, Coffield AB, Flottemesch TJ, Nelson WW, Goodman MJ, Solberg LI. Priorities among effective clinical preventive services: methods. Am J Prev Med. 2006 Jul;31(1):90-6. Review. — View Citation

Tuomilehto J, Lindström J, Eriksson JG, Valle TT, Hämäläinen H, Ilanne-Parikka P, Keinänen-Kiukaanniemi S, Laakso M, Louheranta A, Rastas M, Salminen V, Uusitupa M; Finnish Diabetes Prevention Study Group. Prevention of type 2 diabetes mellitus by changes in lifestyle among subjects with impaired glucose tolerance. N Engl J Med. 2001 May 3;344(18):1343-50. — View Citation

Westfall JM, Mold J, Fagnan L. Practice-based research--"Blue Highways" on the NIH roadmap. JAMA. 2007 Jan 24;297(4):403-6. — View Citation

Williams GC, Grow VM, Freedman ZR, Ryan RM, Deci EL. Motivational predictors of weight loss and weight-loss maintenance. J Pers Soc Psychol. 1996 Jan;70(1):115-26. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The primary outcome measure is weight loss with a goal of 7% of initial weight.		6 months	No
Secondary	Exercising a minimum of 150 minutes per week at a moderate level to maintain an energy expenditure of 700 kcals per week		6 months	No
Secondary	;Fat intake less than 25% and saturated fat less than 10% Fiber intake of at least 25 grams per day;Fasting blood sugar < 100 mg/dL; Absence of tobacco use		6 months	No

External Links

•   Diabetes Prevention Program