A Sensory Strategy to Cut Sugary Beverages in African/American and Latine Adolescents

NCT07223151 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 63

Last updated 2025-10-31

No results posted yet for this study

Summary

The goal of this clinical trial is to test whether replacing sugary sodas with unsweetened, flavored sparkling waters can reduce added sugar intake and improve health in Black/African American and Latine adolescents with obesity who prefer sweet-tasting beverages. The main questions it aims to answer are:

* Does replacing sugary sodas with water change liking for sugary drinks, and water?
* Do shifts in liking for sweetness lead to improved diet quality and cardiometabolic health?

Researchers will compare replacing sugary sodas with one of three alternative beverages: unsweetened sparkling water, plain water, and beverages with gradually reduced sugar to determine which strategy is most effective.

Participants will:

* Replace sugary sodas with study drinks for 4 weeks
* Complete taste tests to measure their liking for and sensory experience of sweetness over 8-weeks
* Provide dietary recalls, body measurements, and blood samples over 8-weeks

Conditions

Interventions

BEHAVIORAL

Unsweetened Sparkling Water Replacement

Participants replace all sugar-sweetened sodas with flavored, unsweetened sparkling waters for 4 weeks.

BEHAVIORAL

Progressively Reduced Sugar Beverage Replacement

Participants replace sugary sodas with beverages containing gradually decreasing sugar concentrations (weekly), ending with unsweetened sparkling water.

BEHAVIORAL

Plain Water Replacement

Participants replace all sugar-sweetened sodas with plain, still water for 4 weeks. This serves as a comparator to evaluate sensory and metabolic changes.

Sponsors & Collaborators

  • Purdue University

    collaborator OTHER
  • Nana Gletsu Miller

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
12 Years
Max Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-07-25
Primary Completion
2027-06-30
Completion
2027-06-30

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07223151 on ClinicalTrials.gov