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Short-term Sugary Beverage Consumption on Glucose Control and Cardiovascular Disease Risk Factors

Effects of Short-term Sugary Beverage Consumption on Type-2 Diabetes and Cardiovascular Disease Risk Factors: A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04118257
Enrollment
37
Registered
2019-10-08
Start date
2017-02-10
Completion date
2018-11-14
Last updated
2019-10-08

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

Conditions

Metabolic Syndrome

Keywords

Glucose control, Cardiovascular disease risk factors, Sugary beverages, Pulmonary function

Brief summary

Our goal is to determine how the addition of sugar-sweetened beverages to the diet affects glucose control, cardiovascular disease risk factors, and pulmonary function in healthy, young adults.

Detailed description

In a 3-arm randomized controlled trial, 36 participants consumed one of three beverages for three weeks: water (W), caffeine-free soda (S), or 100% fruit juice (FJ). Participants consumed two servings/day (\ 710mL) of their randomized beverage for three weeks, along with their habitual diets. At baseline and following the 3-week intervention, participants completed glucose control, cardiovascular disease risk factor, and pulmonary function assessments.

Interventions

DIETARY_SUPPLEMENTSugary beverage: Fruit juice

Participants consumed 100% fruit juice (\ 710mL) daily for three weeks, along with their habitual diets.

DIETARY_SUPPLEMENTSugary beverage: Soda

Participants consumed soda (\ 710mL) daily for three weeks, along with their habitual diets.

DIETARY_SUPPLEMENTControl: Water

Participants consumed water (\ 710mL) daily for three weeks, along with their habitual diets.

Sponsors

Kansas State University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* Free from diagnosis of diabetes and pulmonary illness * Have no intake of glucose or lipid lowering medication.

Exclusion criteria

* Smoke * Currently pregnant * Have bronchitis * Have more than 2 risk factors for cardiovascular disease, as defined by the American College of Sports Medicine (ACSM).

Design outcomes

Primary

MeasureTime frameDescription
Change in glucose iAUCWeek 0 and Week 3Glucose obtained from blood sample in a fasted state and in response to a meal

Secondary

MeasureTime frameDescription
Change in homeostatic model assessment for insulin resistanceWeek 0 and Week 3Calculated from fasting glucose and insulin values
Change in blood pressureWeek 0 and Week 3Evaluated via automated sphygmomanometer.
Change in BMIWeek 0 and Week 3Weight and height will be combined to report BMI in kg/m\^2
Change in plasma lipidsWeek 0 and Week 3Total cholesterol (TC), LDL-c , VLDL-c, HDL-c , triglycerides (TG) from blood sample in a fasted state and following consumption of a meal
Change in insulin iAUCWeek 0 and Week 3Glucose obtained from blood sample in a fasted state and in response to a meal
Change in serum fructosamineWeek 0 and Week 3Fructosamine obtained from blood sample
Change in pulmonary functionWeek 0 and Week 3Assessed using the maximum flow-volume loop

Countries

United States

Outcome results

None listed

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