Actively Recruiting

Age: 18Years +
All Genders
ID06776965

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age > 18 years
  • Diagnosis of chronic rheumatic disease (rheumatoid arthritis, spondyloarthritis, osteoarthritis)
  • Ability to complete questionnaires
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

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

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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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