- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03672578
Reducing Sugar-sweetened Beverage Consumption Among Young Adults
January 18, 2019 updated by: University of California, Davis
This study aims to test sugar-sweetened beverage (SSB) health labeling elements in an online experiment to determine which elements are the most salient among young adults.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
2971
Phase
- Not Applicable
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
-
-
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
Description
Inclusion criteria:
- ≥18 years of age
- current/recent (<1 year of graduation) undergraduate student at 3 specific universities
- English-speaking
- consumes at least 2 SSBs per week
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
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Loss-frame, text-only, no attribution
Label participants will see is loss-frame, text-only, and with no attribution
|
loss frame label
text-only label
label with no attribution
|
|
Experimental: Gain-frame, text-only, no attribution
Label participants will see is gain-frame, text-only, and with no attribution
|
text-only label
label with no attribution
gain frame label
|
|
Experimental: Loss-frame, icon, no attribution
Label participants will see is loss-frame, icon, and with no attribution
|
loss frame label
label with no attribution
label with icon and text
|
|
Experimental: Grain-frame, icon, no attribution
Label participants will see is gain-frame, with an icon, and with no attribution
|
label with no attribution
gain frame label
label with icon and text
|
|
Experimental: Loss-frame, icon, attribution
Label participants will see is loss-frame, icon, and with attribution
|
loss frame label
label with icon and text
label with attribution
|
|
Experimental: Gain-frame, icon, attribution
Label participants will see is grain-frame, icon, and with attribution
|
gain frame label
label with icon and text
label with attribution
|
|
Experimental: Loss-frame, text-only, attribution
Label participants will see is loss-frame, text-only, and with attribution
|
loss frame label
text-only label
label with attribution
|
|
Experimental: Gain-frame, text-only, attribution
Label participants will see is gain-frame, text-only, and with attribution
|
text-only label
gain frame label
label with attribution
|
|
Placebo Comparator: No label
Participant will not see a label
|
No label
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
SSB Intention
Time Frame: Up to 20 minutes
|
Intention to consume SSBs measured by hypothetical selection of a beverage from images of beverage options.
|
Up to 20 minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
SSB Intention (2)
Time Frame: Up to 20 minutes
|
Measured by survey items assessing intention to consume SSBs on a scale from 1 (not at all likely) to 7 (extremely likely).
|
Up to 20 minutes
|
|
SSB attitudes
Time Frame: Up to 20 minutes
|
Measured by survey items assessing perceived healthfulness of SSBs on a scale from 1 (extremely unhealthy) to 7 (extremely healthy).
|
Up to 20 minutes
|
|
SSB knowledge
Time Frame: Up to 20 minutes
|
Measured by survey items assessing knowledge of number of calories (estimate provided by participant) and sugar (estimated by participant, in teaspoons) contained in SSBs.
|
Up to 20 minutes
|
|
SSB norms
Time Frame: Up to 20 minutes
|
Measured by survey item assessing how often participants perceive their peers to consume SSBs (1 = multiple times a day, 2 = daily, 3 = weekly, 4 = less than once a week, and 5 = never) and item on perception that people who are important to the participant would want them to limit SSB intake, on a scale from 1 (not at all) to 5 (completely) .
|
Up to 20 minutes
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
SSB self-efficacy
Time Frame: Up to 20 minutes
|
Measured by survey item assessing how confident participant feels in reducing SSB consumption, on a scale from 1 (not at all) to 5 (completely).
|
Up to 20 minutes
|
|
Social interaction
Time Frame: Up to 20 minutes
|
Measured by survey item assessing likelihood participant will encourage others to reduce SSB consumption, on a scale from 1 (not at all) to 5 (completely).
|
Up to 20 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Jennifer Falbe, ScD, MPH, University of California, 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)
August 18, 2018
Primary Completion (Actual)
November 17, 2018
Study Completion (Actual)
November 17, 2018
Study Registration Dates
First Submitted
September 10, 2018
First Submitted That Met QC Criteria
September 12, 2018
First Posted (Actual)
September 14, 2018
Study Record Updates
Last Update Posted (Actual)
January 23, 2019
Last Update Submitted That Met QC Criteria
January 18, 2019
Last Verified
January 1, 2019
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 1124060
- 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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