NCT07505134

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

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
50

participants targeted

Target at P25-P50 for not_applicable

Timeline
1mo left

Started May 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress78%
May 2026Sep 2026

First Submitted

Initial submission to the registry

March 17, 2026

Completed
15 days until next milestone

First Posted

Study publicly available on registry

April 1, 2026

Completed
1 month until next milestone

Study Start

First participant enrolled

May 1, 2026

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2026

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2026

Expected
Last Updated

May 1, 2026

Status Verified

April 1, 2026

Enrollment Period

3 months

First QC Date

March 17, 2026

Last Update Submit

April 27, 2026

Conditions

Keywords

GLP-1Food choiceCravingsFood cue reactivity

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

EXPERIMENTAL

Advertisements viewed daily by this group will be food and/or beverage products

Behavioral: Food advertisements

Tech advertisement group

PLACEBO COMPARATOR

Individuals in this group will only receive tech-related advertisements daily

Behavioral: Tech advertisements

Interventions

Videos and images of food and beverage advertisements from popular brands and/or restaurants

Food advertisement group

Video and photo advertisements of popular tech tools

Tech advertisement group

Eligibility Criteria

Age18 Years - 85 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

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