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UCSD Take Charge Study

Randomized Clinical Trial of a Weight Loss Program in Type 2 Diabetes

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01345500
Enrollment
227
Registered
2011-05-02
Start date
2012-02-29
Completion date
2013-10-31
Last updated
2013-11-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetic, Obese, Obesity, Overweight, Type 2 Diabetes

Keywords

Overweight, Obese, Type 2 Diabetic, Diabetes, Weight loss, Physical activity, Diet, Prepackaged meals

Brief summary

The purpose of the Take Charge Study is to determine among overweight and obese men and women with type 2 diabetes whether 1) participating in a commercial weight loss program promotes great weight loss and weight loss maintenance at one year compared to usual care conditions and 2) whether there is a differential weight loss response to different dietary macronutrient composition (lower carbohydrate/higher fat diet versus a higher carbohydrate/lower fat).

Interventions

OTHERHigher Carbohydrate, Lower Fat Diet

Study participants will receive prepackaged prepared foods as needed to achieve a meal plan, free-of-charge for a 12-month period. The lower fat, higher carbohydrate diet provides 60% energy from carbohydrate, 20% energy from fat, and 20% energy from protein. The diet falls within the range of current dietary recommendations.

OTHERLower carbohydrate, Higher fat diet

Study participants will receive prepackaged prepared foods as needed to achieve a meal plan, free-of-charge for a 12-month period. The lower carbohydrate, higher fat diet provides 45% energy from carbohydrate, 35% energy from fat, and 20% energy from protein. The diet falls within the range of current dietary recommendations.

OTHERIndividualized Counseling

Participants assigned to the usual care group will be provided consultation with a research staff dietetics professional, who will provide publicly available print material that describes dietary and physical activity guidelines to promote weight loss and maintenance, at baseline (after randomization) and again at 6 months.

Sponsors

HealthPartners Institute
CollaboratorOTHER
University of Minnesota
CollaboratorOTHER
University of California, San Diego
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Aged 18 years or older * Type 2 diabetes * BMI 25-45 kg/m2 * Willing to participate in any of the study diet arms (higher or lower carbohydrate diet or usual care) over a one-year period * Able to comply with all required study procedures and schedule * Must live within the San Diego or Minneapolis area

Exclusion criteria

* Pregnant, breastfeeding or planning to become pregnant in the next year * Serious medical condition or psychiatric illness * History of having an eating disorder, food allergy or food intolerance * Have food restrictions or requires a special diet * Objects to frozen, processed or prepackaged foods * Inability to be moderately physically active * Currently enrolled in a weight loss program or another diet intervention * Current use of weight loss medication or supplements * Planned surgical procedure that can impact the conduct of the study * Previous surgical procedures for weight reduction * Does not have own transportation * Have plans to relocate from area within 1 year * HbA1C \>11%, fasting triglycerides \>600 mg/dL, serum creatinine \>1.4 mg/dL (women) or 1.5 mg/dL (men) -- to be screened at baseline visit

Design outcomes

Primary

MeasureTime frameDescription
Total weight loss1 yearTo test, in a randomized controlled trial, whether participation in a commercial weight loss program promotes greater weight loss and weight loss maintenance at one year in overweight or obese men and women with type 2 diabetes compared to usual care conditions.

Secondary

MeasureTime frameDescription
Response to macronutrient composition1 yearTo examine whether there is a differential weight loss response at 3, 6 and/or 12 months to different dietary macronutrient composition (higher carbohydrate and lower fat versus lower carbohydrate and higher fat) in the weight loss intervention in these overweight or obese men and women with type 2 diabetes.
Biochemical/social outcomes1 yearTo describe the effect of participating in the program (vs. usual care) on markers of glycemic control, cardiovascular disease risk, cardiopulmonary fitness, plasma carotenoids, quality of life, and eating attitudes and behaviors. Also to examine whether there is a differential response to different dietary macronutrient composition in the two weight loss intervention groups in selected metabolic factors, lipids and CRP at 6 and 12 months.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026