Young Adult Beverage and Health Study

September 25, 2019 updated by: University of California, Davis
This study examines the impact of health signage on beverage consumption in a cafeteria.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Actual)

911

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • United States
    • California
      • Davis, California, United States, 95616
        • University of California, Davis

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

At specific university: Undergraduate college students on meal plan and university staff

Description

Inclusion Criteria:

  • Undergraduate student or staff member at specific university
  • Age 18+
  • On meal plan if a student
  • Works in specific cafeterias if staff

Exclusion Criteria:

  • Age <18 years
  • Adults unable to consent or complete the written or online survey

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Comparison
Cohort of participants who regularly eat in cafeteria without health signage.
Signage
Cohort of participants who regularly eat in cafeteria in which health signage is placed.
Behavioral: Signage
Placement of signage discouraging consumption of beverages with added sugar

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in self-reported sugar-sweetened beverage consumption
Time Frame: 5 months
Beverage frequency questionnaire assessing whether various beverages were consumed "4 or more times per day," "3 times per day," "2 times per day," "1 time per day," "4-6 times per week," "2-3 times per week," "one time per week or less," or "never" in the last/current semester.
5 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in cafeteria sugar-sweetened beverage usage
Time Frame: 5 months
Based on inventory and syrup/beverage purchase data and customer counts.
5 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

University of California, Davis

Collaborators

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
University of California, Berkeley

Investigators

  • Principal Investigator: Jennifer Falbe, ScD, MPH, UC Davis

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 24, 2018

Primary Completion (Actual)

May 21, 2019

Study Completion (Actual)

May 21, 2019

Study Registration Dates

First Submitted

January 18, 2019

First Submitted That Met QC Criteria

January 22, 2019

First Posted (Actual)

January 24, 2019

Study Record Updates

Last Update Posted (Actual)

September 27, 2019

Last Update Submitted That Met QC Criteria

September 25, 2019

Last Verified

September 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • 1124060-2
  • 1K01DK113068-01A1 (U.S. NIH Grant/Contract)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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