Type 2 Diabetes Clinical Trial
Official title:
Egg Ingestion in Adults With Type 2 Diabetes: Effects on Glycemic Control, Anthropometry, Diet Quality and Cardiometabolic Status A Randomized, Controlled, Crossover Trial
| Verified date | November 2017 |
| Source | Griffin Hospital |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
We propose a prospective, randomized, single-blind controlled crossover study to assess the effects of daily egg inclusion versus egg exclusion, on glycemic control, anthropometric measures, and overall diet quality in adults with Type 2 diabetes.
| Status | Completed |
| Enrollment | 32 |
| Est. completion date | November 2015 |
| Est. primary completion date | November 2015 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 35 Years and older |
| Eligibility |
Inclusion Criteria: - males age greater than 35 years; - post-menopausal females not currently on hormone replacement therapy; - non-smokers; - clinical diagnosis of Type 2 diabetes mellitus for at least 1 year but no more than 5 years; - 6.5% = HbA1c =8.0% (5) BMI between 25 and 40 kg/m². Exclusion Criteria: - failure to meet inclusion criteria; - anticipated inability to complete study protocol for any reason; - current eating disorder; - use of antihyperglycemic, lipid-lowering or antihypertensive medications unless stable on medication for at least 3 months; - use of glucocorticoids, antineoplastic agents, psychoactive agents, or nutraceuticals; - regular use of fiber supplements; - restricted diets (i.e., vegetarian, vegan, gluten free); - known allergy to eggs. |
| Country | Name | City | State |
|---|---|---|---|
| United States | Yale-Griffin Prevention Research Center | Derby | Connecticut |
| Lead Sponsor | Collaborator |
|---|---|
| Griffin Hospital | American Egg Board |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Glycemic Index | Glycated hemoglobin A1c (HbA1c) will be used to measure the average plasma glucose concentration. | 12-weeks | |
| Secondary | Fasting glucose and insulin | Glucose and insulin will be measured at each time point. Participants will be asked to fast at least 8 hours before glucose and insulin measurement. Homeostasis Model Assessment (HOMA-IR) values will be calculated from fasting serum glucose and serum insulin levels using HOMA calculator version 2.2.1 to gauge the degree of insulin resistance. | 12-weeks | |
| Secondary | Body Composition | Body composition will be measured using bioelectrical impedance analysis, which uses the resistance of electrical flow through the body to estimate body fat. The Tanita SC-240 Body Composition Analyzer will be used to measure body composition. The SC-240 Body Composition Analyzer measures weight and calculates body fat% and total body water% in addition to BMI. | 12- weeks | |
| Secondary | Body Weight | Body weight will be measured during each visit. It will be measured to the nearest 0.5 pound using a balance-type medical scale. Subjects will be measured in the morning (fasting), unclothed with the exception of undergarments. | 12- weeks | |
| Secondary | Waist Circumference | Waist circumference will be measured using the U.S. government standard protocol. It will be measured around the narrowest point between ribs and hips when viewed from the front after exhaling. | 12-weeks | |
| Secondary | Diet Quality | To help the study team track any variation in dietary pattern over the course of the study, all participants will be asked at two time points to provide information on the foods and beverages that they consumed during a 3-day period. For each 3-day period, participants will complete three 24-hour recalls using a web-based Automated Self-Administered 24-Hour Recall (ASA24) (available from the National Cancer Institute at http://riskfactor.cancer.gov/tools/instruments/asa24/) which will guide them through the process of completing the recall data. Diet quality will be assessed using the Alternative Healthy Eating Index (AHEI). 3-day food period data will be collected at baseline, 6 weeks and 12 weeks. | Baseline, 6-weeks, 12-weeks | |
| Secondary | Physical Activity | Physical activity will be determined by the Seven-Day Physical Activity Recall [PAR]. The PAR is one of the most widely used physical activity assessments in exercise science and epidemiological research. The popularity of this measure stems largely from its versatility and relative ease of use for research applications. The PAR provides detail regarding the duration, intensity, and volume (energy expenditure) of physical activity and can therefore be used for a variety of applications. Because it utilizes a one-week time frame, the data from the PAR is often considered representative of typical activity patterns. While it requires considerable cognitive effort by the participants, the interviewer administered version can be completed in a reasonable amount of time (~20 minutes). Variation in physical activity level will be controlled in our multivariable regression models. | 12-weeks |
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