CClinicalTrials.gg
CompletedNCT07368855Updated Jan 27, 2026

GLP-1 Medicines and Mental Health Changes

An interventional study of GLP-1 in Obesity, Depression and GLP-1, sponsored by University of California, San Diego. Completed at 1 site in United States. Per ClinicalTrials.gov, last updated 2026-01-27.

Sponsored by University of California, San Diego · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 1 year 8 months after the study started (first participant enrolled May 2024, registered Jan 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
90
Allocation
Not applicable
Sex
All
01

Study summary

Key question: Is the use of GLP-1 weight loss medicines - semaglutide and tirzepatide - associated with improvements in mental health and health-related quality of life?

Key finding: Across six- months of GLP-1 treatment, participants reported statistically significant improvements in mental health, eating disorder symptoms, and health-related quality of life domains such as pain interference and sleep quality.

Message for readers: Although GLP-1 medicines are prescribed primarily for weight loss and metabolic health benefits, growing evidence suggests that these medicines may also facilitate meaningful improvements in mental health and quality of life.

Read the detailed description

In a sample of veterans with obesity and established metabolic disease receiving supervised GLP-1 treatment for weight loss, we observed a consistent pattern of improved psychiatric health, eating disorder behaviors, and health-related quality of life. In addition to observing statistically significant changes across all the latter dimensions using validated psychometric measures, effect size magnitudes were also large enough to suggest potentially clinically meaningful improvements. Importantly, we observed robust evidence of decreases in depressive symptoms - averaging 30% declines in symptom severity - with no signs of increased suicidal ideation symptoms in the sample. The smaller size of this sample necessarily warrants additional research to validate these findings across the broader veteran population and among non-veteran samples.

02

Conditions studied

  • Obesity
  • Depression
  • GLP-1

Keywords

  • Veterans, obesity, GLP-1, depression, mental health
03

In context

Obesity

6,297 studies on the registry are indexed under Obesity; 1,693 are open to participants now.

This study's enrollment of 90 is above the median of 78 across 4,879 interventional studies indexed under Obesity.

Browse Obesity studies →

Lead sponsor

University of California, San Diego is the lead sponsor of 958 studies on the registry; 191 are open to participants now.

Of its 110 completed or terminated interventional studies of FDA-regulated products, 70 (64%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Veterans receiving care at the VA San Diego Healthcare System

Exclusion criteria

Exclusion Criteria:

  • VASDHS Veterans not receiving GLP-1 medicines for obesity through the weight control clinic
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
90 participants (actual)

Study arms

  • Other
    GLP-1 medicine

    GLP-1 treatment

    Drug: GLP-1

Interventions

  • DrugGLP-1

    Wegovy or Zepbound

06

What researchers measure

Primary outcomes

  1. Beck Depression Inventory-2

    Changes in BDI-2 scores

    Time frame: Six months

07

Study locations

1 site
  • VA San Diego Healthcare System
    San Diego, California 92161, United States
08

References and documents

Individual participant data

Plan to share: No — Data belong to VA San Diego and are not mine to share.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 27, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07368855
Lead sponsor
University of California, San Diego
Responsible party
Thomas Rutledge (Professor in Residence/Staff Psychologist, University of California, San Diego) — Principal investigator
First posted
Jan 27, 2026
Start date
May 1, 2024
Primary completion
Jul 1, 2025
Completion
Jul 1, 2025
Last update
Jan 27, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2026. You cannot join it, but the record below documents what was studied.

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