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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03771261
Acronym
EGGSPDITe
Enrollment
99
Registered
2018-12-11
Start date
2018-06-15
Completion date
2021-11-08
Last updated
2023-09-11

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

Conditions

Obesity, Pre Diabetes

Keywords

Egg, Protein, Aging, Health Disparities, Weight Loss

Brief 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.

Detailed 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.

Interventions

BEHAVIORALWeight Loss

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

DIETARY_SUPPLEMENTEgg Protein

Participants will be provided pre-packaged hard-boiled eggs (3/day, medium) and egg white protein powder.

Sponsors

Egg Nutrition Center
CollaboratorOTHER
Duke University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline Insulin Resistance at 4 months0 to 4 monthsBlood glucose and insulin levels in whole blood will be used to compute HOMA-IR (= glucose mg/dL x insulin mg/dL/405)
Change from Baseline Body weight at 4 months0 to 4 monthsWeight loss as measured in light clothing on a dedicated scale.

Secondary

MeasureTime frameDescription
Change from baseline 8-foot up and Go time at 4 months0 to 4 monthsTime it takes to get up from a chair walk around a cone and sit back down (8-foot up and go)
Change from baseline 30-second chair stands (number of stands) at 4 months0 to 4 monthsthe number of chair stands completed in 30 seconds
Change from baseline handgrip strength at 4 months0 to 4 monthsthe highest weight achieved from 2 attempts using the JAMAR dynamometer
Change from baseline grooved pegboard time at 4 months0 to 4 monthsmeasure of hand dexterity, time it takes to fit pegs into grooved pegboard
Change from baseline fat mass (%) at 4 months0 to 4 monthsBody fat mass (%) as measured by Bodpod
Change from baseline fat mass (kgs) at 4 months0 to 4 monthsBody fat mass (kg) as measured by Bodpod
Change from baseline lean mass (kgs) at 4 months0 to 4 monthsBody lean mass (kg) as measured by Bodpod
Change from baseline lean mass (%) at 4 months0 to 4 monthsBody lean mass (%) as measured by Bodpod
Change from baseline minimal waist circumference at 4 months0 to 4 monthsBody 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.
Change from baseline umbilical waist circumference at 4 months0 to 4 monthsBody 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.
Change from baseline Short Physical Performance Battery at 4 months0 to 4 monthsPhysical Performance as measured by Short Physical Performance Battery (SPPB)
Change from baseline total calories at 4 months0 to 4 monthsTotal calories will be measured using 3-day food records (participants record everything they eat and drink for three days)
Change from baseline macronutrient intake at 4 months0 to 4 monthsMacronutrient intake will be measured using 3-day food records (participants record everything they eat and drink for three days)
Change from baseline micronutrient intake at 4 months0 to 4 monthsMicronutrient intake will be measured using 3-day food records (participants record everything they eat and drink for three days)
Change from baseline Symbol digit modalities test at 4 months0 to 4 monthsSymbol Digit Modalities Test measures cognitive impairment
Change from baseline Trail Making Test at 4 months0 to 4 monthsTrail 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.
Change from baseline Hopkins Verbal Learning Test at 4 months0 to 4 monthsHopkins Verbal Learning Test consists of three trials of free-recall of a 12-item, semantically categorized list, followed by yes/no recognition.
Change from baseline Profile of Mood States at 4 months0 to 4 monthsProfile 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.
Change from baseline Perceived Stress Scale at 4 months0 to 4 monthsPerceived 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.
Change from Baseline Insulin Sensitivity at 4 months0 to 4 monthsinsulin sensitivity HOMA-β (= 360 x insulin mg/dL / glucose mg/dL - 63; %).
Change from baseline hip circumference at 4 months0 to 4 monthsBody 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.
Change from baseline 6-minute walk (meters) at 4 months0 to 4 monthsDistance (meters) walked in 6 minutes

Countries

United States

Outcome results

None listed

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