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The Effects of GLP-1 Receptor Agonists on Chemosensory Function and Ingestive Behavior
The Effects of GLP-1 Receptor Agonists on Sensory Systems and Ingestive Behavior
Lead sponsor
Asset
GLP-1 / incretin class catch-all
Listed sites
1
Recruiting sites
—
Enrollment
90
actual
Study population
Obesity / overweight
Key I/E criterion
•BMI ≥30
Primary endpoints
•Taste Detection Thresholds•Suprathreshold Taste Intensity•Taste Hedonics
Footprint
Where this trial recruits
Site locations as reported to ClinicalTrials.gov. Site count is not enrollment count; per-site enrollment is not available from source.
Identifiers
Registered as
Timeline
Milestones
Assets
Investigational agents
Study populations
Who this study enrolls
Eligibility
Who can enroll
Study population text
Adults aged 18 to 65 years with a Body Mass Index (BMI) greater than 30 kg/m² will be recruited. The study population includes individuals who are eligible to take GLP-1 receptor agonists but have not yet started treatment, and individuals who have been taking GLP-1 receptor agonists for weight management for approximately 1 month or approximately 6 months as part of their regular medical care. Participants will be recruited from the general population and through healthcare providers at IU Health.
Inclusion criteria
Exclusion criteria
Endpoints (11)
What's being measured
Protocol endpoints and posted registry outcome measures, grouped into outcome categories. Composite endpoints show their component event types. Standard codes (LOINC, SNOMED CT) are shown where available.
Coverage by outcome category
Patient-reported / QoL
2 endpointsFood Preferences
Time frame:During study participation, up to 2 weeks
descriptive
Questionnaire-Based Measures of Food Cravings, Food Cue Responsivity, Food Noise, and Eating Behavior
Time frame:During study participation, up to 2 weeks
descriptive
Other (unclassified)
9 endpointsTaste Detection Thresholds
Time frame:During study participation, up to 2 weeks
descriptive
Suprathreshold Taste Intensity
Time frame:During study participation, up to 2 weeks
descriptive
Taste Hedonics
Time frame:During study participation, up to 2 weeks
descriptive
Fat Taste Intensity Rating
Time frame:During study participation, up to 2 weeks
descriptive
ArOMa-T Olfactory Test Performance
Time frame:During study participation, up to 2 weeks
descriptive
SCENTinel Olfactory Test Performance
Time frame:During study participation, up to 2 weeks
descriptive
Attentional Bias to Food Cues
Time frame:During study participation, up to 2 weeks
descriptive
Dietary Intake
Time frame:During study participation, up to 2 weeks
descriptive
Cephalic-Phase Salivary Response
Time frame:During study participation, up to 2 weeks
descriptive
Publications (1)
Bibliography
Records linked to this trial through ClinicalTrials.gov references, PubMed NCT search, and curated study seeds. 'Canonical' marks design/result papers; others are registry references or candidates.
Registry references + supporting bibliography
- The Journal of clinical endocrinology and metabolism2020 May 1PMID31665455doi:10.1210/clinem/dgz140via CT.gov background
Provenance
Sources
Trial facts come from public ClinicalTrials.gov records. Endpoint categories are Delfa's classification of those records, not a ClinicalTrials.gov field. All figures reflect the July 1, 2026 snapshot.