GLP-1 drugs vs. nutrition counseling for Psoriatic Arthritis with obesity and diabetes
Official title: Impact of Glucagon-like Peptide-1 (GLP-1) Analogs on Disease Outcomes in Psoriatic Arthritis: A Pragmatic Randomized Controlled Trial
Run by Medical College of Wisconsin · NCT07111494 · Data updated 2026-11-12
This trial compares GLP-1 medications to nutrition counseling to see which approach best helps adults with psoriatic arthritis who also have obesity and type 2 diabetes.
Quick facts
| Phase | Phase 4 |
|---|---|
| Study type | Interventional |
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 22 (estimated) |
| Sponsor | Medical College of Wisconsin Academic / other |
| Locations | 1 site (Milwaukee, Wisconsin) |
| Status | Recruiting |
| Started | May 1, 2026 |
| Main results expected | October 15, 2027 |
| Study ends | October 15, 2028 |
| Registry record updated | November 5, 2026 |
| Trial ID | NCT07111494 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults 18 years or older with CASPAR-confirmed PsA, BMI ≥30, ongoing PsA treatment, and insufficient disease control (not in minimal disease activity).
✕Probably not a fit
Patients who do not respond to GLP-1 therapy or nutrition counseling, or those with contraindications to GLP-1 agents, may not experience benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is a pragmatic randomized controlled trial in adults with psoriatic arthritis who also have obesity and diabetes. Participants will be randomized to receive a GLP-1 agonist or structured nutrition counseling, aiming to improve disease activity and overall health. The study focuses on real-world applicability, with up to four in-person visits over 24 weeks and collection of both clinical and patient-reported outcomes. Eligibility requires CASPAR-confirmed PsA, BMI ≥30, inadequate disease control, and FDA-appropriate GLP-1 eligibility. Primary goals include disease outcomes and patient-reported measures under the two treatment approaches.
Why it matters
Potential benefit: If successful, patients could experience reduced psoriatic arthritis activity and improved metabolic health through either a GLP-1–based strategy or optimized nutrition counseling.
How similar studies have gone: Prior studies suggest metabolic interventions can influence inflammatory arthritis outcomes, but direct convergence with GLP-1 therapy in PsA is less established and represents a novel approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adult patients (age 18 and older) who present to rheumatology clinic * Participants must be able to read, understand, and provide documented informed consent as approved by the Institutional Review Board (IRB). * Meet the Classification of Psoriatic Arthritis (CASPAR) criteria for PsA * Participants must have a Body Mass Index (BMI) of 30kg/m\^2 * Participants must be treated for PsA in accordance with guidelines * Have not achieved MDA in PsA patients * Have a minimum TJC \> 1 and SJC \> at baseline * Eligible for GLP-1 agonist treatment in accordance with Food Drug Administration (FDA) labeling as determined by the investigator. Exclusion Criteria: * Any prior use of GLP-1 agonists * Inability to provide informed consent * Current participation in another PsA study * Treatment initiation by GLP-1 agonists contraindicated by FDA * Patients with hemoglobin A1c (HbA1c) \> 10 at baseline
Where it's running
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Medical College of Wisconsin/Froedtert Hosptial
Milwaukee, Wisconsin, United States Recruiting
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.