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Weight Loss Diet Study: Low Carb vs Low Fat

Weight Loss Diet Study: Low Carbohydrate vs. Low Fat and Insulin Resistance Status

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01661426
Enrollment
61
Registered
2012-08-09
Start date
2012-04-30
Completion date
2013-03-31
Last updated
2023-02-22

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

Conditions

Obesity, Insulin Resistance

Keywords

Adults, Weight loss, Diet, Insulin Resistance, Fatty acid composition

Brief summary

The traditional weight loss diet recommended by health professionals has been a low-fat, high-carbohydrate, calorie restricted diet. This recommendation has been challenged by a number of alternative dietary strategies, particularly low-carbohydrate diets. In several recent weight loss studies insulin resistant adults had more success with low- vs. high-carbohydrate diets, in contrast to insulin sensitive adults who had either more success or comparable success with the low-fat diets. The investigators enrolled 61 people with a wide range of insulin sensitivity/resistance. After determining their insulin resistance status, the investigators will split them in the middle and randomly assign them to one of four groups for six months: (1) Low-Carbohydrate/Insulin Resistant (LC/IR); (2) Low-Carbohydrate/Insulin Sensitive (LC/IS); (3) Low-Fat/Insulin Resistant (LF/IR); and (4) Low-Fat/Insulin Sensitive (LF/IS) (15 people/group). After 6 months the participants will switch diet for the following 6 months, i.e. those randomized to the Low-Carbohydrate diet will switch to the Low-Fat diet and vice-versa. The primary outcome of this study is to determine whether weight loss success can be increased if one follows the dietary approach appropriately matched to their insulin resistance status. Secondary outcomes include fasting insulin, glucose, lipids, and fatty acid composition. \--------------------------------------------------------------------------------

Detailed description

The investigators hope to learn whether matching the weight loss diet to one's insulin resistance status will increase weight loss the success. The relevance of these findings is highlighted by the fact that the national recommendations for weight loss are to follow a high-carbohydrate, low-fat diet. This would imply that about half the population has been given the wrong advice in regards to the most successful dietary pattern for weight loss. Plasma fatty acid composition patterns have been shown to be associated with both insulin resistance and/or carbohydrate intake. As secondary analyses, the investigators will explore: (1) differences in plasma fatty acid composition between insulin sensitive and resistant participants at baseline; (2) the correlations between insulin markers and plasma fatty acid composition at baseline; (3) the interaction between insulin status and diet on 6-month changes in the plasma fatty acid composition; (4) plasma fatty acid composition changes in participants on low fat and low carbohydrate diets after 6 months; and (5) the correlations between changes in insulin markers, dietary components, and plasma fatty acid composition after 6 months.

Interventions

Counseling/instruction on how to follow a healthy low-carbohydrate diet for 6 months. One evening class/week for 8 weeks (8 total classes). Then one class every other week for 8 weeks (4 total classes). Then one class every four weeks for 8 weeks (2 total classes): 14 evening classes, total.

BEHAVIORALLow-Fat Diet

Counseling/instruction on how to follow a healthy low-fat diet for 6 months. One evening class/week for 8 weeks (8 total classes). Then one class every other week for 8 weeks (4 total classes). Then one class every four weeks for 8 weeks (2 total classes): 14 evening classes, total.

Sponsors

Hass Avocado Board
CollaboratorOTHER
Stanford University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Intervention model description

The study employed a 2 x 2 crossover design: LF vs. LC diets and more IR vs. more IS. Study participants were classified as more IR or more IS based on the median AUC for insulin concentrations measured from an oral glucose tolerance test (OGTT) prior to randomization. Participants above the median were considered more IR and those below the median were considered more IS. A random number generator was used to stratify the randomization to LF vs. LC by insulin resistance status and gender. Participants followed their assigned diet for 6 months and then switched to the opposite diet for another 6 months.

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Age: \> or = 18 years of age * Women: Pre-menopausal (self-report) and \<50 years of age * Men: \<50 years of age * Race/Ethnicity: All * BMI (body mass index): 28-40 kg/m2 (need to lose \>10% body weight to achieve healthy BMI) * Body weight stable for the last two months, and not actively on a weight loss plan * No plans to move from the area over the next 14 months * Available and able to participate in the evaluations and intervention for the study period * Willing to accept random assignment * To enhance study generalizability, people on medications not noted below as specific exclusions can participate if they have been stable on such medications for at least three months * Ability and willingness to give written informed consent * No known active psychiatric illness

Exclusion criteria

* Pregnant, lactating, within 6 months post-partum, or planning to become pregnant in the next 12 months; no menstruation for the previous 12 months * Diabetes (type 1 and 2) or history of gestational diabetes or on hypoglycemic medications for any other indication * Prevalent diseases: Malabsorption, renal or liver disease, active neoplasms, recent myocardial infarction, hypertension (except for those stable on hypertensive medications) (\<6 months) (patient self-report and, if available, review of labs from primary care provider) * Smokers (because of effect on weight and lipids) * History of serious arrhythmias, or cerebrovascular disease * Uncontrolled hyper- or hypothyroidism (TSH not within normal limits) * Medications: Lipid lowering, diabetes medications, and those known to affect weight/energy expenditure * Excessive alcohol intake (self-reported, \>3 drinks/day)

Design outcomes

Primary

MeasureTime frameDescription
Change in weightBaseline and 12 monthsWeight change was calculated as the 12 month value minus the baseline value

Secondary

MeasureTime frameDescription
Change in insulin AUCBaseline and 12 monthsInsulin area under the curve (AUC) change was calculated as the 12 month value minus the baseline value.
Change in Fasting GlucoseBaseline and 12 monthsFasting glucose change was calculated as the 12 month value minus the baseline value.
Change in LDL-CholesterolBaseline and 12 monthsLDL-cholesterol change was calculated as the 12 month value minus the baseline value.
Change in HDL-CholesterolBaseline and 12 monthsHDL-cholesterol change was calculated as the 12 month value minus the baseline value.
Change in TriglyceridesBaseline and 12 monthsTriglycerides change was calculated as the 12 month value minus the baseline value.
Change in Fasting InsulinBaseline and 12 monthsFasting insulin change was calculated as the 12 month value minus the baseline value
Plasma fatty acid composition at baselineBaselineComparison of the plasma fatty acid composition between insulin sensitive and resistant participants at baseline.
Correlations between insulin markers and plasma fatty acid composition at baseline.Baseline
Interaction between insulin status and diet on 6-month changes in the plasma fatty acid composition.6 months
Comparison of plasma fatty acid composition changes in participants on low fat and low carbohydrate diets after 6 months.Baseline and 6 months
Correlations between changes in insulin markers, dietary components, and plasma fatty acid composition after 6 months.6 months
Change in systolic and diastolic blood pressureBaseline and 12 monthsBlood pressure change was calculated as the 12 month value minus the baseline value.

Countries

United States

Outcome results

None listed

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