- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02947802
Sugar Sweetened Beverage Labeling Support
October 3, 2023 updated by: Leslie John, Harvard University
This is an online survey assessing consumer support for different labeling policies related to sugar sweetened beverages.
The investigators will present consumers with three labels that are being considered for sugar sweetened beverages: a calorie label, a text warning label that says "Warning drinking beverages with added sugar(s) can lead to health problems like obesity, diabetes and tooth decay" and a graphic warning label that includes graphic images to correspond with each of the health problems listed with the text warning.
The investigators will ask participants their support for each label.
The investigators will also see if support for the labels change after learning of the effectiveness of these labels.
The investigators will share the results of a recent field study that suggested calorie and textual warning labels had no influence on the purchasing of sugar sweetened beverages while the graphic label decreased purchasing by 11 percent.
Study Overview
Status
Completed
Conditions
Study Type
Interventional
Enrollment (Actual)
400
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
-
-
Massachusetts
-
Cambridge, Massachusetts, United States, 02163
- Harvard University
-
-
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
Description
Inclusion Criteria:
- The investigators will recruit a nationally representative sample using ClearVoice, a company that recruits online survey takers.
Exclusion Criteria:
-
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: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Consumer Support
Participants will be presented with three labels: a calorie label, a textual warning label and a textual warning label with corresponding graphic images and will be asked to rate their support for each label on a 1 (not at all) to 7 (a great deal) scale.
|
In one of our parallel assigned conditions participants will receive no additional information and be asked to rate their support for the label.
|
Experimental: Consumer Support with Effectiveness Info
Participants will be presented with three labels: a calorie label, a textual warning label and a textual warning label with corresponding graphic images and will be asked to rate their support for each label on a 1 (not at all) to 7 (a great deal) scale.
Participants will also receive effectiveness information- how each label influenced the purchasing of sugar sweetened beverages- from a recent field experiment.
|
In one of our parallel assigned conditions participants will receive additional information (e.g., an intervention) of effectiveness information.
These consumers will learn how effective these labels were in reducing the purchasing of sugar sweetened beverages in a recent study.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Rate Support of a Label on a 1 (not at all) to 7 (a great deal) Scale.
Time Frame: Immediately following the presentation of the labels.
|
Participants will rate their support of the label on a 1 (not at all) to 7 (a great deal)
|
Immediately following the presentation of the labels.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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
October 1, 2016
Primary Completion (Actual)
November 1, 2016
Study Completion (Actual)
November 1, 2016
Study Registration Dates
First Submitted
October 26, 2016
First Submitted That Met QC Criteria
October 26, 2016
First Posted (Estimated)
October 28, 2016
Study Record Updates
Last Update Posted (Actual)
October 4, 2023
Last Update Submitted That Met QC Criteria
October 3, 2023
Last Verified
October 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- IRB16-1585
Plan for Individual participant data (IPD)
Study Data/Documents
-
Study Instrument (Online Survey)
Information comments: This is the online survey participants will complete.
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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