AzTrials
AzTrials

Type 2 DiabetesSODASNCT03944616

Study Of Drinks With Artificial Sweeteners in People With Type 2 Diabetes

A study testing Diet Beverage and Water in people with Type 2 Diabetes, run by University of California, Irvine at 2 sites in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

Diet beverages sweetened with artificial sweeteners occupy a unique category in the food environment as they are a source of intensely sweet taste with no calories. Diet beverages are the single largest contributor to artificial sweetener intake in the U.S. Read more about this study

Who is it for?
Ages 35 years and older
Conditions the study is for
Type 2 Diabetes
What is being tested?
Diet Beverage and Water
Could I receive a placebo?
No, everyone receives an active treatment
How many people
181 participants
Where
2 sitesUnited States
Study dates
6 Jun 2019to 21 Mar 2024
Phase
Interventional
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 35 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

None listed.

Who cannot join

  • Type 1 diabetes or suspected type 1 diabetes (lean with polyuria, polydipsia, and weight loss with little response to metformin)
  • "Secondary" diabetes due to specific causes (e.g. monogenic syndromes, pancreatic surgery, and pancreatitis)
  • Diabetic Ketoacidosis hospitalization within last 6 months
  • Severe/major hypoglycemia in the last 3 months-severe/major hypoglycemia is defined as a hypoglycemic event in which patient requires assistance of another person to manage the episode
  • Glucocorticoid use (prednisone 2.5 mg/d or more or its equivalent)
  • History of intolerance or allergy to diet beverages or AS or phenylketonuria
Show all 20Show fewer
  • Any condition that is known to affect the validity of the glycemic measures (Hba1c)
  • Major cardiovascular disease event or surgery within past 6 months
  • Gastrointestinal disease
  • Renal or liver disease
  • Current treatment for cancer
  • Those with major surgery planned or history of bariatric surgery
  • Antibiotic treatment (> 6 days) within past 6 months
  • Currently pregnant (via self-report) or planning to become pregnant during study period; <1 year postpartum and breast feeding
  • Current participation in another interventional clinical trial
  • Previous randomization in this study,
  • Heavy alcohol consumption (on average >2 drinks/day for women and >3 drinks/day for men)
  • Habitual consumer of SSB ≥ 1 serving / day (8 oz.)
  • Does not drink diet beverages
  • BMI < 20.0 kg/m2

Trial locations and contacts

2 sites in 1 country.

United States2 sites
  • University of California, Irvine

    Irvine, California, 92697

  • University of Minnesota

    Minneapolis, Minnesota, 55454

Other trials in United States

About this study

Official title: Effect of Artificially Sweetened Beverages on Diabetes Control in Adults With Type 2 Diabetes

Diet beverages sweetened with artificial sweeteners occupy a unique category in the food environment as they are a source of intensely sweet taste with no calories. Diet beverages are the single largest contributor to artificial sweetener intake in the U.S. diet, and people with diabetes are the highest consumers of diet beverages, tending to consume them as a replacement for dietary sources of sugar, especially in place of sugar-sweetened beverages. This behavior has been endorsed by dietetic and scientific organizations, and diet beverages are marketed as being synonymous with better health, suitable for weight loss, and thus advantageous for diabetes control. The underlying public health concern is that there are few data to support or refute the benefit or harm of habitual diet beverage consumption by people with diabetes; therefore randomized trials with relevant outcomes must be conducted because they would address many limitations of previous research and have major implications for dietary recommendations on diet beverage intake and primary and secondary prevention of chronic disease. To begin addressing this important scientific gap the investigators are testing the effect of diet beverage intake on diabetes control parameters in free-living adults with type 2 diabetes in a randomized, two arm parallel trial with a run-in period of 2-weeks and an active intervention period of 24-weeks. This study will recruit 200 patients with type 2 diabetes who are usual consumers of commercial diet beverages and randomize them to receive and consume either: 1) A commercial diet beverage of choice (3 servings or 24 oz. daily); or 2) Unflavored bottled water of choice (sparkling or plain) (3 servings or 24 oz. daily). The primary outcome will be a central measure of clinical diabetes control in glycated hemoglobin (HbA1c). The study will also measure the nature and magnitude of glycemic excursions via continuous glucose monitors, as well as clinical markers of cardiometabolic risk and kidney function. Lastly, investigators will measure plausible mechanisms whereby diet beverage intake may alter risk by assessing the effect of diet beverage intake on the functional composition of the gut microbiome via stool samples and comprehensive metabolomics, satiety hormones, as well as usual dietary intake, and upstream behavioral pathways which may inform dietary intake patterns.

Conditions
Type 2 Diabetes
Being tested
Diet Beverage, Water
Keywords
Diet beverages, diet, diabetes control, artificial sweeteners, continuous glucose monitor, gut microbiome, metabolomics
Medical subject headings
Diabetes Mellitus, Type 2

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Diet BeverageBehavioural

    Participants will receive and consume three daily servings (24 ounces) of a non-caloric commercial diet beverage of their choice sweetened with FDA approved artificial sweeteners.

  • WaterBehavioural

    Participants will receive and consume three daily servings (24 ounces) of plain bottled/canned water in place of their usual commercial diet beverage. The water will be unflavored, unsweetened, non-caloric, and may be plain or sparkling. Participants randomized to consume water will be instructed to avoid intake of diet beverages.

Study groups in NCT03944616
Study groupRoleWhat they receive
Diet BeverageActive comparatorParticipants will receive and consume three daily servings (24 ounces) of a non-caloric commercial diet beverage of their choice sweetened with FDA approved artificial sweeteners.
Receives: Behavioral: Diet Beverage
WaterExperimentalParticipants will receive and consume three daily servings (24 ounces) of plain bottled/canned water in place of their usual commercial diet beverage. The water will be unflavored, unsweetened, non-caloric, and may be plain or sparkling. Participants randomized to consume water will be instructed to avoid intake of diet beverages.
Receives: Behavioral: Water

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. HbA1c

    Glycated hemoglobin

    Measured: Time 0 (directly after 2-week run-in), 12, 24 weeks

Secondary outcomes (25)
  1. Time In Range

    Time in range is collected by a masked Continuous Glucose Monitor (CGM), which measures individual glucose levels every 15 minutes for two weeks via a sensor placed on the participants upper arm (underside). Time in Range is defined as the % of time each day with a glucose measure between 70-180 mg/dl. The range of CGM data for inclusion in this study will be 5 to 14 days, consistent with manufacturer's recommendations.

    Measured: All 14 day periods: Run-in (2-weeks, usual-baseline), weeks 11 and 12 (14 days), weeks 23 and 24 (14 days)

  2. Glycemic Variability

    Glycemic variability is collected by a masked Continuous Glucose Monitor (CGM), which measures individual glucose levels every 15 minutes for two weeks via a sensor placed on the participants upper arm (underside). Glycemic variability is defined as the Standard Deviation (SD) of the mean glucose during the wear period. The range of CGM data for inclusion in this study will be 5 to 14 days, consistent with manufacturer's recommendations.

    Measured: All 14 day periods: Run-in (2-weeks, usual-baseline), weeks 11 and 12 (14 days), weeks 23 and 24 (14 days)

  3. Mean Glucose (mg/dl)

    A measure of the mean, 24 hour glucose concentration calculated across all recorded glucose readings during the wear period

    Measured: All 14 day periods: Run-in (2-weeks, usual-baseline), weeks 11 and 12 (14 days), weeks 23 and 24 (14 days)

  4. Fasting Glucose

    Standard (mg/dl) measure taken fasting (morning) during baseline, 12 weeks, 24 weeks

    Measured: Time 0 (directly after 2-week run-in), 12, 24 weeks

  5. Fasting Insulin (Pmol/L)

    Standard lab measurement for fasting insulin assessment

    Measured: Time 0 (directly after 2-week run-in), week 12, week 24

  6. Fructosamine

    Fructosamine (umol/L) represents usual glycemia over the past 2-3 weeks, and is considered a valid marker of short term clinical glycemic patterns by the American Diabetes Association

    Measured: Time 0 (directly after 2-week run-in),12, 24 weeks

  7. Weight (kg)

    Weight measured on standardized scale in gown

    Measured: Time 0 (directly after 2-week run-in), 12, 24 weeks

  8. Total Cholesterol (mg/dL)

    Total cholesterol was measured as part of a lipid panel, a standard measurement for assessing clinical CVD risk

    Measured: Time 0 (directly after 2-week run-in), 12, 24 weeks

  9. Kidney Function

    eGFR-Cystatin-C (estimated glomerular filtration rate) = mL/min/1.73 m^2

    Measured: Time 0 (directly after 2-week run-in),12, 24 weeks

  10. Systolic Blood Pressure

    Systolic blood pressure (mmHg)

    Measured: Time 0 (directly after 2-week run-in),12, 24 weeks

  11. Diastolic Blood Pressure

    Standard part of blood pressure measurement (mmHG)

    Measured: Time 0 (directly after 2-week run-in), 12, 24 weeks

  12. Apolipoprotein-AI

    Apo-AI the major protein component of high density lipoprotein (HDL)

    Measured: Time 0 (directly after 2-week run-in), 12, 24 weeks

  13. Apolipoprotein B

    ApoB levels indicate the atherogenic particle concentration independent of the particle cholesterol content

    Measured: Time 0 (directly after 2-week run-in), 12, 24 weeks

  14. Fibrinogen (mg/dL)

    A protein involved in forming blood clots in the body

    Measured: Time 0 (directly after 2-week run-in), 12, 24 weeks

  15. C-reactive Protein

    biomarker of inflammation

    Measured: Time 0 (directly after 2-week run-in), 12, 24 weeks

  16. Aspartate Aminotransferase (AST) (U/L)

    AST (aspartate aminotransferase) is an enzyme that reflects liver function

    Measured: Time 0 (directly after 2-week run-in), 12, 24 weeks

  17. Aminotransferase (ALT) (U/L)

    ALT (alanine transaminase) is an enzyme, a protein that reflects liver function

    Measured: Time 0 (directly after 2-week run-in), 12, 24 weeks

  18. Alkaline Phosphatase (ALKPhos ) (U/L)

    ALP is an enzyme, a protein, that reflects liver function

    Measured: Time 0 (directly after 2-week run-in), 12, 24 weeks

  19. Thyroid Stimulating Hormone (TSH)

    Hormone measured in the blood with energy balance related role

    Measured: Time 0 (directly after 2-week run-in), 12, 24 weeks

  20. Dietary Quality (Healthy Eating Index -HEI)

    The Healthy Eating Index (HEI) is a measure of diet quality used to assess how well a set of foods aligns with key recommendations and dietary patterns published in the Dietary Guidelines for Americans (Dietary Guidelines). The overall HEI scores are made up of 13 components that reflect the different food groups and key recommendations in the Dietary Guidelines for Americans. The HEI is scored 0-100 (low to high), with higher scores representing greater reported intake of an overall dietary pattern aligning with USDA Dietary Guidelines. In the SODAS study, dietary intake was assessed by multiple unannounced 24-hour dietary recalls that occurred during the 2-week run-in period to assess usual habits (2 recalls over 2 weeks) and the active intervention (5 recalls over 24 weeks: 2 to 3 recalls during weeks 1-12 (period 1), and 2 to 3 recalls during weeks 13-24 (period 2). to measure any changes in diet quality. Scores during each period represent the average score of recalls.

    Measured: Run-in period (2 weeks) - baseline, Week 1-12 (period 1), Week 13-24 (period 2).

  21. The Diabetes Health Profile (DHP-18)

    The Diabetes Health Profile (DHP-18) is used to assess health related quality of life in diabetes across three domains (psychological distress, barriers to activity and disinhibited eating). Each item is scored on a 4-point scale, and the subscale scores are then rescaled to a 0-100 range, with higher scores indicating poorer well-being.

    Measured: Time 0 (directly after 2-week run-in), 12, 24 weeks

  22. Food Craving Inventory (FCI)

    The FCI is a valid and reliable self-report measure of specific food cravings. The inventory consists of 4 factors or subscales measuring cravings for high fats (8 items), carbohydrates/starches (8 items), sweets (8 items), and fast food fats (4 items), and a total score is calculated by summing the subscales. Participants rate each food on a 5-point Likert scale ranging from 0 (never) to 4 (always/almost every day). We calculated the total score by summing the individual item responses in each subscale. Higher scores indicate more frequent cravings of the 28 items.

    Measured: Time 0 (directly after 2-week run-in), 12, 24 weeks

  23. The Pittsburgh Sleep Quality Index (PSQI)

    The Pittsburgh Sleep Quality Index (PSQI) is a self-report questionnaire that assesses sleep quality over a one-month time interval. Each component score of the PSQI ranges from 0 to 3, with 3 indicating the greatest dysfunction or disturbance. The seven component scores are then summed to obtain a global PSQI score, which ranges from 0 to 21. Higher scores indicate poorer sleep quality, with a score greater than 5 suggesting significant sleep difficulties

    Measured: Time 0 (directly after 2-week run-in), 12, 24 weeks

  24. Medication Effect Score (MES)

    The medication effect score (MES) is a measure of overall diabetes regimen intensity, and is based on the dosages of medications used and their potencies. The MES is calculated for each diabetes medication in a regimen using the following equation: (actual drug dose/maximum drug dose) × drug-specific adjustment factor. The adjustment factor equates to the expected decrease in HbA1c achieved by the drug as monotherapy. The MES presumes a linear relationship between medication dosage and HbA1c, and the sum of MES values attributed to individual medications represents the maximum A1c reduction that may be expected by the regimen. It is a continuous variable with range 0 (no medications), and the maximum achievable MES is patient specific and dependent on the total number of and dose of medications reported.

    Measured: Time 0 (directly after 2-week run-in), 6, 12, 18, 24 weeks

  25. Therapeutic Intensity Score (TIS)

    The therapeutic intensity score (TIS) is a summary measure that accounts for the number of medications and the relative doses a patient received to lower blood pressure. It is a continuous variable with range 0 (no medications), and the maximum achievable TIS is patient specific and dependent on the total number of antihypertensive medications reported.

    Measured: Time 0 (directly after 2-week run-in), 6, 12, 18, 24 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted9 May 2019
  2. Study start6 Jun 2019
  3. Primary completion21 Mar 2024
  4. Study completion21 Mar 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Model description
This study is testing the effect of commercial diet beverage intake on diabetes control parameters in free-living adults with type 2 diabetes in a randomized, two arm parallel trial with a run-in period of 2-weeks and an active intervention period of 24-weeks. We will recruit 200 patients with type 2 diabetes who are usual consumers of commercial diet beverages and randomize them to receive and consume either: 1) A commercial diet beverage of choice (3 servings or 24 oz. daily); or 2) Unflavored bottled water of choice (sparkling or plain) (3 servings or 24 oz. daily).
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
181 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03944616
Sponsor's protocol ID
20184756
Other IDs
1R01DK117028-01A1
Acronym
SODAS
Status last verified
Sep 2025
First submitted
19 Nov 2018
Last updated
11 Sep 2025
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: It is not yet known if there will be a plan to make IPD available.

Questions about this trial

What is this clinical trial studying?

A study testing Diet Beverage and Water in people with Type 2 Diabetes, run by University of California, Irvine at 2 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 0 inclusion and 20 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 11 Sep 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Yes. Results are posted in the registry (first posted 11 Sep 2025). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

HbA1c (time frame: Time 0 (directly after 2-week run-in), 12, 24 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Sep 2025.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in