Exploring the Influence of Glucagon-like Peptide -1 (GLP-1) Medications on Food Cravings, Food Selection, and Food Intake Following Exposure to Food Advertisements
Exploring the Influence of GLP-1 Medications on External Food Cue Reactivity and Resultant Food Choice and Intake
1 other identifier
interventional
50
0 countries
N/A
Brief Summary
The purpose of this randomized control trial is to compare how food cravings, food selection, and food consumption change in response to frequent food advertisements compared to non-food advertisements in adults taking GLP-1 (weight loss) medications. The primary question we aim to answer is: do GLP-1 medications reduce an individual's vulnerability to external triggers that drive food cravings and consumption? Participants will:
- report daily food consumption for a total of 10 days,
- receive eight daily prompts to view food or non-food related advertisements, and respond to a short 9-question survey for 7 days,
- answer several questionnaires,
- and complete two in-person visits to complete a virtual reality food selection task.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started May 2026
Shorter than P25 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 17, 2026
CompletedFirst Posted
Study publicly available on registry
April 1, 2026
CompletedStudy Start
First participant enrolled
May 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2026
ExpectedMay 1, 2026
April 1, 2026
3 months
March 17, 2026
April 27, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (5)
Mean food cue reactivity scores in the afternoon
Average scores of craving levels for each group following afternoon advertisement viewing sessions
7-day period of all afternoon survey responses
Mean food cue reactivity scores in the morning
Average scores of craving levels for each group following morning advertisement viewing sessions
7-day period of all morning survey responses
Mean food cue reactivity scores in the evening
Average scores of craving levels for each group following evening advertisement viewing sessions
7-day period of all evening survey responses
Mean food cue reactivity scores overall
Average scores of craving levels for each group over all viewing sessions
7-day period of all survey responses
Energy density of consumed foods
The energy density profile of foods consumed each day
7 days
Secondary Outcomes (5)
Change from baseline in energy density of foods selected in the virtual buffet
Baseline and 7 days
Changes in food noise since being on medication questionnaire
Baseline
Changes in reasons for purchasing foods questionnaire
Baseline
Individual Food Cue Responsiveness--Trait
Baseline
Change in brand familiarity, liking, and/or craving
Baseline and 7 days
Study Arms (2)
Food advertisement group
EXPERIMENTALAdvertisements viewed daily by this group will be food and/or beverage products
Tech advertisement group
PLACEBO COMPARATORIndividuals in this group will only receive tech-related advertisements daily
Interventions
Videos and images of food and beverage advertisements from popular brands and/or restaurants
Video and photo advertisements of popular tech tools
Eligibility Criteria
You may qualify if:
- Adults (18+) with overweight or obesity (BMI \>25 kg/m2)
- On an injectable form of tirzepatide GLP-1 medication at a minimum dose of 7.5 mg, taking it as prescribed by their doctor
- Not currently taking an incretin-based medication at baseline other than the GLP-1 medication
- Fluent in English
You may not qualify if:
- Do not have consistent access to a smart phone that can access the study software
- Diagnosed with cognitive or physical disability or epilepsy
- Adults taking a compound GLP-1
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Penn State Universitylead
- Penn State Healthcollaborator
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor and Director of the Health, Ingestive Behavior, and Technology Lab
Study Record Dates
First Submitted
March 17, 2026
First Posted
April 1, 2026
Study Start
May 1, 2026
Primary Completion
August 1, 2026
Study Completion (Estimated)
September 1, 2026
Last Updated
May 1, 2026
Record last verified: 2026-04