Actively Recruiting
Impact of Ultra-processed Foods in Patients With Chronic Rheumatic Diseases Including Rheumatoid Arthritis, Spondyloarthritis, and Osteoarthritis
Led by Hospices Civils de Lyon · Updated on 2025-04-11
240
Participants Needed
1
Research Sites
34 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying the consumption of ultra-processed foods (UPF) in people with chronic rheumatic diseases like rheumatoid arthritis, spondyloarthritis, and osteoarthritis. These foods may affect disease activity by changing gut bacteria, increasing intestinal permeability, and interacting with the immune system. The study aims to understand UPF consumption patterns and how they relate to disease activity in these conditions. Participants include groups with rheumatoid arthritis, spondyloarthritis, osteoarthritis, and a control group without rheumatic disease. The study involves self-administered dietary questionnaires and disease activity assessments at the start, 6 months, and 12 months. These tools will help track UPF consumption and disease symptoms over time. During the study, participants complete questionnaires about their diet and disease activity at three timepoints. Researchers will analyze these responses to describe UPF intake and its possible links to disease activity. The main outcome is the description of UPF consumption at baseline. The total study duration for each participant is 12 months, with safety and disease activity monitored throughout.
CONDITIONS
Brief Title
Ultra Processed Foods Consumption and Impact in Rheumatic Diseases.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age > 18 years
- Diagnosis of chronic rheumatic disease (rheumatoid arthritis, spondyloarthritis, osteoarthritis)
- Ability to complete questionnaires
You will not qualify if you...
- Under judicial protection
- Refusal to participate in the study
- Having two rheumatic diseases at the same time
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 12 months
Participants complete self-administered dietary and disease activity questionnaires at multiple timepoints to observe their consumption of ultra-processed foods and disease status.
3 visits (baseline, 6 months, and 12 months)
Trial Site Locations
Total: 1 location
1
Edouard Herriot Hospital
Lyon, France, 69003
Actively Recruiting
Research Team
M
Maxime AUROUX, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
4
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