Balanced (Egg) Protein During Obesity Reduction: Differential Responses of Insulin Resistance by Race

Obesity Clinical Trial

— EGGSPDITe  

Official title:

Balanced (Egg) Protein During Obesity Reduction: Differential Responses of Insulin Resistance by Race

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03771261
• Other study ID #: Pro00089075
• Status: Completed
• Phase: N/A
• Start date: June 15, 2018
• Est. completion date: November 8, 2021

Study information

• Verified date: January 2022
• Source: Duke University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of the trial is to assess the effects of combining regular, generous intakes of high quality protein (with substantial amounts provided from whole eggs and egg whites) with calorie restriction on insulin resistance and weight loss (along with function, body composition, racial disparities, and a number of secondary outcomes) in black and white older adults with prediabetes who are participating in a 4-month intervention. The investigators will compare these effects to the same outcomes with a control group consuming a traditional control regimen of calorie restriction over the same duration.

Description:

Older (>60 yrs) men and women (50% African American, 50% white) who are obese (BMI >30 kg/m2) and have pre-diabetes will be randomly assigned (1:1 ratio; couples randomized together) to one to two treatment groups: 1) Weight loss intervention (WL-Control; n = 20): subjects follow a calorie-reduction diet for a weight loss of ≥10%, protein~0.8g/g/d; and 2) High protein weight loss intervention (WL-Protein; n = 20): subjects follow a calorie-reduction diet for a weight loss of ≥10%, with a high proportion of high quality protein (> 30g protein, 3/day, 60-70% egg protein). Primary (insulin resistance/sensitivity, weight loss) and secondary outcomes (physical function, body composition, diet adherence, cognitive function, readiness to change) will be measured at 0 and 4 months.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 99
• Est. completion date: November 8, 2021
• Est. primary completion date: November 5, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 60 Years and older

Eligibility

Inclusion Criteria:

• Age > 60 years

• Identifies as Caucasian/white or African-American/black

• Obese body weight (>30 kg/m2)

• Able to speak and understand spoken and written English

• Elevated fasting plasma glucose (=95 and <126 mg/dL)

• Age-normal Kidney function (= 45 mL/min/1.73 m2)

Exclusion Criteria:

• Body weight > 224 kg (limit of the BodPod)

• Treated or untreated diabetes (prior diagnosis, treatment, or fasting blood glucose =126 mg/dL)

• Presence of unstable, acutely symptomatic, or life-limiting illness

• Positive screen for dementia using Mini-Cog evaluation tool

• Neurological conditions causing functional or cognitive impairments

• History of significant weight instability (defined as > 10 pounds weight gain or loss over 6 months prior to study participation)

• Allergy or intolerance to egg products

• Unwillingness or inability to be randomized to any one of two intervention groups, submit to all study testing, or continuously participate in a randomly assigned lifestyle intervention program for four months

• Inability to walk independently

• Unable to give consent

• Unable to complete written recording forms including journals of eating and exercise behaviors.

• Current use of the following medications: monoamine oxidase inhibitors, prescription weight loss medications, insulin, metformin or any other hypoglycemic agent

• Primary Care Physician advises against participation

• Smoker

• Unusually or unstable renal function

Related Conditions & MeSH terms

• Insulin Resistance
• Obesity
• Pre Diabetes
• Prediabetic State

Intervention

Behavioral:
• Weight Loss
Participants will be prescribed hypo-caloric diet by a registered dietitian and attend weekly social support/nutrition education meetings.

Dietary Supplement:
• Egg Protein
Participants will be provided pre-packaged hard-boiled eggs (3/day, medium) and egg white protein powder.

Locations

Country	Name	City	State
United States	Duke University Medical Center	Durham	North Carolina

Sponsors (2)

Lead Sponsor	Collaborator
Duke University	Egg Nutrition Center

Country where clinical trial is conducted

United States, 

References & Publications (3)

Porter Starr KN, McDonald SR, Bales CW. Obesity and physical frailty in older adults: a scoping review of lifestyle intervention trials. J Am Med Dir Assoc. 2014 Apr;15(4):240-50. doi: 10.1016/j.jamda.2013.11.008. Epub 2014 Jan 17. — View Citation

Porter Starr KN, McDonald SR, Weidner JA, Bales CW. Challenges in the Management of Geriatric Obesity in High Risk Populations. Nutrients. 2016 May 4;8(5):262. doi: 10.3390/nu8050262. — View Citation

Porter Starr KN, Pieper CF, Orenduff MC, McDonald SR, McClure LB, Zhou R, Payne ME, Bales CW. Improved Function With Enhanced Protein Intake per Meal: A Pilot Study of Weight Reduction in Frail, Obese Older Adults. J Gerontol A Biol Sci Med Sci. 2016 Oct;71(10):1369-75. doi: 10.1093/gerona/glv210. Epub 2016 Jan 18. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change from Baseline Insulin Resistance at 4 months	Blood glucose and insulin levels in whole blood will be used to compute HOMA-IR (= glucose mg/dL x insulin mg/dL/405)	0 to 4 months
Primary	Change from Baseline Body weight at 4 months	Weight loss as measured in light clothing on a dedicated scale.	0 to 4 months
Secondary	Change from baseline Short Physical Performance Battery at 4 months	Physical Performance as measured by Short Physical Performance Battery (SPPB)	0 to 4 months
Secondary	Change from baseline 6-minute walk (meters) at 4 months	Distance (meters) walked in 6 minutes	0 to 4 months
Secondary	Change from baseline 8-foot up and Go time at 4 months	Time it takes to get up from a chair walk around a cone and sit back down (8-foot up and go)	0 to 4 months
Secondary	Change from baseline 30-second chair stands (number of stands) at 4 months	the number of chair stands completed in 30 seconds	0 to 4 months
Secondary	Change from baseline handgrip strength at 4 months	the highest weight achieved from 2 attempts using the JAMAR dynamometer	0 to 4 months
Secondary	Change from baseline grooved pegboard time at 4 months	measure of hand dexterity, time it takes to fit pegs into grooved pegboard	0 to 4 months
Secondary	Change from baseline fat mass (%) at 4 months	Body fat mass (%) as measured by Bodpod	0 to 4 months
Secondary	Change from baseline fat mass (kgs) at 4 months	Body fat mass (kg) as measured by Bodpod	0 to 4 months
Secondary	Change from baseline lean mass (kgs) at 4 months	Body lean mass (kg) as measured by Bodpod	0 to 4 months
Secondary	Change from baseline lean mass (%) at 4 months	Body lean mass (%) as measured by Bodpod	0 to 4 months
Secondary	Change from baseline minimal waist circumference at 4 months	Body proportions will be measured at the minimal waist using a Gulick II tape measure with the tape placed directly on the skin (not over the clothing). Measurements will be taken once at each location before completing a second measurement, and an average of the two will be recorded. A third measurement will be taken if the first two measurements are > 0.5 cm.	0 to 4 months
Secondary	Change from baseline umbilical waist circumference at 4 months	Body proportions will be measured at the umbilical waist using a Gulick II tape measure with the tape placed directly on the skin (not over the clothing). Measurements will be taken once at each location before completing a second measurement, and an average of the two will be recorded. A third measurement will be taken if the first two measurements are > 0.5 cm.	0 to 4 months
Secondary	Change from baseline hip circumference at 4 months	Body proportions will be measured at the hip using a Gulick II tape measure with the tape placed directly on the skin (not over the clothing). Measurements will be taken once at each location before completing a second measurement, and an average of the two will be recorded. A third measurement will be taken if the first two measurements are > 0.5 cm.	0 to 4 months
Secondary	Change from baseline total calories at 4 months	Total calories will be measured using 3-day food records (participants record everything they eat and drink for three days)	0 to 4 months
Secondary	Change from baseline macronutrient intake at 4 months	Macronutrient intake will be measured using 3-day food records (participants record everything they eat and drink for three days)	0 to 4 months
Secondary	Change from baseline micronutrient intake at 4 months	Micronutrient intake will be measured using 3-day food records (participants record everything they eat and drink for three days)	0 to 4 months
Secondary	Change from baseline Symbol digit modalities test at 4 months	Symbol Digit Modalities Test measures cognitive impairment	0 to 4 months
Secondary	Change from baseline Trail Making Test at 4 months	Trail Making Test neuropsychological test of visual attention and task switching. It consists of two parts in which the subject is instructed to connect a set of 25 dots as quickly as possible while still maintaining accuracy.	0 to 4 months
Secondary	Change from baseline Hopkins Verbal Learning Test at 4 months	Hopkins Verbal Learning Test consists of three trials of free-recall of a 12-item, semantically categorized list, followed by yes/no recognition.	0 to 4 months
Secondary	Change from baseline Profile of Mood States at 4 months	Profile of Mood States is a psychological rating scale used to assess transient, distinct mood states that uses a five-point scale ranging from "not at all" to "extremely".	0 to 4 months
Secondary	Change from baseline Perceived Stress Scale at 4 months	Perceived Stress Scale is a a 12-item stress assessment instrument. Individual scores on the PSS can range from 0 to 40 with higher scores indicating higher perceived stress.	0 to 4 months
Secondary	Change from Baseline Insulin Sensitivity at 4 months	insulin sensitivity HOMA-ß (= 360 x insulin mg/dL / glucose mg/dL - 63; %).	0 to 4 months

External Links

•   Duke University School of Medicine
•   Egg Nutrition Center