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Completed

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

Purdue University

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 ThresholdsSuprathreshold Taste IntensityTaste 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

NCT IDNCT07611201
Org study IDIRB-2024 - 1407

Timeline

Milestones

Study start2025-02-20actual
Primary completion2026-05-04actual
Study completion2026-05-04actual
Study first posted2026-05-28actual
Last update posted2026-05-28actual

Assets

Investigational agents

Study populations

Who this study enrolls

Obesity / overweight

Eligibility

Who can enroll

Minimum age18 Years
Maximum age65 Years
SexAll
Healthy volunteersAccepted
Sampling methodNon probability sample

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

Ages 18 to 65 years.
Any sex or gender.
Body Mass Index (BMI) >30 kg/m².
Stable medication use, excluding weight management medications other than GLP-1 receptor agonist use as part of regular medical care.
Eligible to take GLP-1 receptor agonists but not yet started treatment, or currently taking GLP-1 receptor agonists for weight management for approximately 1 month (±0.5 months) or approximately 6 months (±0.5 months).
No known sensitivity or allergy to study solutions or foods, including sweet solutions, salty solutions, sour solutions, bitter solutions, fatty stimuli, common food flavors used in testing, milk, and fruit-flavored beverages.

Exclusion criteria

Younger than 18 years or older than 65 years.
Previous bariatric surgery or planned bariatric surgery within the next year.
Sensitivity or allergy to study foods, taste solutions, odor stimuli, or food-related test materials.

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

Other (unclassified)
9
Patient-reported / QoL
2

Patient-reported / QoL

2 endpoints
Secondary/protocol endpoint

Food Preferences

Time frame:During study participation, up to 2 weeks

descriptive

Secondary/protocol endpoint

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 endpoints
Primary/protocol endpoint/low confidence

Taste Detection Thresholds

Time frame:During study participation, up to 2 weeks

descriptive

Primary/protocol endpoint/low confidence

Suprathreshold Taste Intensity

Time frame:During study participation, up to 2 weeks

descriptive

Primary/protocol endpoint/low confidence

Taste Hedonics

Time frame:During study participation, up to 2 weeks

descriptive

Primary/protocol endpoint/low confidence

Fat Taste Intensity Rating

Time frame:During study participation, up to 2 weeks

descriptive

Primary/protocol endpoint/low confidence

ArOMa-T Olfactory Test Performance

Time frame:During study participation, up to 2 weeks

descriptive

Primary/protocol endpoint/low confidence

SCENTinel Olfactory Test Performance

Time frame:During study participation, up to 2 weeks

descriptive

Secondary/protocol endpoint/low confidence

Attentional Bias to Food Cues

Time frame:During study participation, up to 2 weeks

descriptive

Secondary/protocol endpoint/low confidence

Dietary Intake

Time frame:During study participation, up to 2 weeks

descriptive

Secondary/protocol endpoint/low confidence

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

Provenance

Sources

Trial identity, design, statusClinicalTrials.gov API v2
Snapshot dateJuly 1, 2026
Endpoint classificationDelfa endpoint taxonomy v2 (May 13, 2026)
Results tableno registry results posted yet

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.