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Ultra Processed Foods Consumption and Impact in Rheumatic Diseases. (NUTRIRIC)

Civil Hospices of Lyon logo

Civil Hospices of Lyon

Status

Enrolling

Conditions

Osteoarthritis
Spondyloarthritis
Rheumatoid Arthritis

Treatments

Other: Evaluation of disease activity (DAS-28, ASDAS, EVA, number of swollen joints, number of painful joint, nocturnal pain, morning stiffness)
Other: Dietary Questionnaire

Study type

Observational

Funder types

Other

Identifiers

NCT06776965
2024-A02327-40 (Other Identifier)
69HCL24_0947

Details and patient eligibility

About

Ultra-processed foods (UPF) represent one of the mainstays of today's diet. They are defined by the NOVA classification system. It was demonstrated that UPF consumption was associated with activity of inflammatory bowel diseases with underlying mechanisms not fully identified yet. It is suspected that UPF constituents could modify the gut microbiota, increase intestinal barrier permeability and directly engage immune surveillance systems, effects that could individually or synergistically increase the risk of immunomediated diseases. As some pathophysiological mechanisms are shared among IBD and rheumatic diseases, we have wondered if UPF consumption could be associated with increased risk of rheumatic disease and/or with their activity.

Our primary aim will be to study the pattern of UPF consumption in patients with rheumatic diseases. Our secondary objectives will be to study the activity of diseases according to UPF consumption.

Enrollment

240 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age > 18 years
  • chronic rheumatic disease (Rheumatoid arthritis, spondyloarthritis, osteoarthritis)
  • ability to perform questionnaires

Exclusion criteria

  • Judicial protection measure
  • Refusal to participate in the study
  • Suffering from 2 rheumatic disease simultaneously

Trial design

240 participants in 4 patient groups

Rheumatoid Arthritis
Description:
Patients in the first group will correspond to those with rheumatoid arthritis according to ACR criteria of RA
Treatment:
Other: Dietary Questionnaire
Other: Evaluation of disease activity (DAS-28, ASDAS, EVA, number of swollen joints, number of painful joint, nocturnal pain, morning stiffness)
Spondyloarthritis
Description:
Patients in the second group will correspond to those with spondyloarthritis according ASDAS criteria
Treatment:
Other: Dietary Questionnaire
Other: Evaluation of disease activity (DAS-28, ASDAS, EVA, number of swollen joints, number of painful joint, nocturnal pain, morning stiffness)
Osteoarthritis
Description:
Patients in the third group will correspond to those with spondyloarthritis according ACR criteria
Treatment:
Other: Dietary Questionnaire
Other: Evaluation of disease activity (DAS-28, ASDAS, EVA, number of swollen joints, number of painful joint, nocturnal pain, morning stiffness)
Controls
Description:
Patients without rheumatic disease
Treatment:
Other: Dietary Questionnaire
Other: Evaluation of disease activity (DAS-28, ASDAS, EVA, number of swollen joints, number of painful joint, nocturnal pain, morning stiffness)

Trial contacts and locations

1

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Central trial contact

Maxime AUROUX, MD

Data sourced from clinicaltrials.gov

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