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Strawberry Consumption in Overweight and Obese Individuals

NCT04094103 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 48

Last updated 2025-09-02

No results posted yet for this study

Summary

Our proposal represents an integrated approach to determining the cardiovascular and metabolic effects of strawberry consumption in adults who have high risk for cardiometabolic disease.

Conditions

Interventions

DIETARY_SUPPLEMENT

Active strawberry powder

Participants will drink a strawberry beverage with active ingredients once a day during the 4-week intervention period.

DIETARY_SUPPLEMENT

Placebo strawberry powder

Participants will drink a strawberry placebo beverage once a day during the 4-week intervention period.

DIETARY_SUPPLEMENT

Mixed strawberry powder

Participants will drink a mixed strawberry beverage with active ingredients and placebo once a day during the 4-week intervention period.

Sponsors & Collaborators

  • California Strawberry Commission

    collaborator OTHER

  • Carl Ade, M.S., Ph.D.

    lead OTHER

Principal Investigators

  • Sara Rosenkranz, PhD · Kansas State University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
35 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-10-01
Primary Completion
2023-10-27
Completion
2023-10-27

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

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 NCT04094103 on ClinicalTrials.gov