AzTrials
AzTrials

NutritionNCT07346001

Impacts of Sugar Warnings on Weight Bias

A study testing Added sugar warning in people with Nutrition and Diet Interventions, run by University of North Carolina, Chapel Hill at 1 site in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
Search all trials

Trial summary

This study aims to examine the effects of added sugar warning labels for sugar-sweetened beverages (SSBs) on explicit weight bias and body weight attributional judgements. Participants will be assigned to view either control labels or added sugar warning labels applied on SSBs in an experimental store. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Nutrition, Diet Interventions
What is being tested?
Added sugar warning
Could I receive a placebo?
No, everyone receives an active treatment
How many people
543 participants
Where
1 siteUnited States
Study dates
16 Feb 2026to Dec 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • 18 years and older
  • Bought sugary drinks from a store at least once during the past week
  • Willing to attend 4 in-person study appointments

Who cannot join

  • Living in the same household as someone else in the study

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Aline D'Angelo Campos, PhD, MPP contact

9199663215

adangelo-campos@unc.edu

United States1 site, 1 recruiting
  • UNC MiniMart Chapel Hill

    Chapel Hill, North Carolina, 27514

    Violet Noe, 252-714-3572, violetn@email.unc.edu

    Recruiting

Other trials in United States

About this study

Official title: Impacts of Prolonged Exposure to Added Sugar Warning Labels on Explicit Weight Bias: a Randomized Controlled Trial

This study aims to examine the effects of added sugar warning labels for sugar-sweetened beverages (SSBs) on explicit weight bias and body weight attributional judgements. Participants will be assigned to view either control labels or added sugar warning labels applied on SSBs in an experimental store. Participants will shop for beverages in the store and take a computer survey during four visits to the store, spaced approximately one week apart.

Read the detailed description

This study aims to determine whether applying added sugar warnings on sugary drinks impacts explicit weight bias and body weight attributional judgements. Approximately 543 adults (ages 18 and older) who have bought at least one SSB in the past week will attend four in-person visits at an experimental store, spaced approximately one week apart. Participants will be randomized to see either neutral control labels or added sugar labels on SSB containers during their visits to the experimental store. At each study visit, participants will shop for beverages in the store and take a computer survey. Explicit weight bias and attribution of responsibility for body weight will be assessed via the computer surveys at the first and last visit.

Being tested
Control label, Added sugar warning

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Control labelBehavioural

    The control label will display a neutral, square-shaped barcode. Labels will be placed on the front of SSB containers in the experimental store.

  • Added sugar warningBehavioural

    The added sugar warning will be octagon-shaped and will state "HIGH IN ADDED SUGAR." Warnings will be placed on the front of SSB containers in the experimental store.

Study groups in NCT07346001
Study groupRoleWhat they receive
Control labelOtherNot described
Receives: Behavioral: Control label
Added sugar warningExperimentalNot described
Receives: Behavioral: Added sugar warning

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Explicit weight bias, mean score

    Explicit weight bias will be measured by survey through seven items. Items will present participants with pairs of antonyms and ask that they select the box between antonyms that they feel best describes their feelings and beliefs about people with obesity: (1) lazy - hard-working, (2) no will power - has will power, (3) good self - control - poor self-control, (4) active - inactive, (5) self-indulgent - self-sacrificing, (6) dislikes food - likes food, (7) undereats - overeats.

    Response options, which will be presented as 5 boxes between antonyms, will be coded in a categorical 1-5 range, where higher scores represent higher endorsement of a stereotype that contributes to weight bias. Each participant's responses to each item will then be averaged across the seven items to obtain their final score on the outcome in a 1-5 range, where higher scores represent higher explicit weight bias.

    Measured: Assessed via survey after exposure to intervention (i.e., shopping task) 2 times approximately 4 weeks apart (i.e., in visits 1 and 4)

Secondary outcomes (1)
  1. Body weight attributional judgements, mean score

    Body weight attributional judgements will be measured by survey through two items. Items will ask participants how much they agree with two statements: (1) People with obesity are responsible for their weight; (2) People with obesity are to blame for their weight.

    Response options will be on a 5-point scale from strongly disagree to strongly agree, with higher scores representing higher agreement. Each participant's responses to each item will be averaged to obtain their final score on the outcome in a 1-5 range, where higher scores represent higher attribution of personal responsibility for body weight.

    Measured: Assessed via survey after exposure to intervention (i.e., shopping task) 2 times approximately 4 weeks apart (i.e., in visits 1 and 4).

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted16 Jan 2026
  2. Study start16 Feb 2026
  3. Primary completionDec 2027 (estimated)
  4. Study completionDec 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
543 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07346001
Sponsor's protocol ID
24-0901b
Status last verified
Apr 2026
First submitted
6 Jan 2026
Last updated
16 Apr 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: The Study Protocol and Statistical Analysis Plan will be shared prior to data collection. After data collection and analysis, a de-identified version of individual participant data and the analytic code will be shared through the Open Science Framework (OSF).

Questions about this trial

What is this clinical trial studying?

A study testing Added sugar warning in people with Nutrition and Diet Interventions, run by University of North Carolina, Chapel Hill at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 16 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Aline D'Angelo Campos, PhD, MPP (9199663215, adangelo-campos@unc.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Explicit weight bias, mean score (time frame: Assessed via survey after exposure to intervention (i.e., shopping task) 2 times approximately 4 weeks apart (i.e., in visits 1 and 4)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Apr 2026.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in