RECRUITING

Anti-Inflammatory Dietary Intervention for Rheumatoid Arthritis

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The primary objective of this study is to assess if there is a significant difference in the mean disease activity score in individuals with RA participating in a dietary intervention compared to those in the control group measured by DAS-28. Other measures to track disease activity will include monitoring number and severity of disease flares and any changes in medications. This will be done by completing a single-blinded randomized controlled trial, parallel in design. The study population will consist of adults diagnosed with Seropositive and Seronegative RA based on the American College of Rheumatology criteria. Participants will have low, moderate, or high disease activity based on DAS-28 where the investigator feels that they can see improvement from a dietary intervention.

Official Title

Anti-Inflammatory Dietary Intervention for Rheumatoid Arthritis

Quick Facts

Study Start:2022-07-05
Study Completion:2025-03
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05291299

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Age greater than 18 years.
  2. * Diagnosed RA by a rheumatologist determined by the 2010 ACR/EULAR Classification Criteria.
  3. * Low, moderate, or highly active disease state based on clinical assessment where the investigator feels there is potential to see a difference.
  4. * Able to read and write in English.
  1. * Younger than 18 years.
  2. * Unable to attend the 8 weekly nutrition appointment.
  3. * History of documented eating disorders.

Contacts and Locations

Study Contact

Natalie Fortune, MS
CONTACT
3106520010
research.admin@attunehealth.com

Study Locations (Sites)

Attune Health Research Inc
Beverly Hills, California, 90211
United States

Collaborators and Investigators

Sponsor: Attune Health Research, Inc.

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-07-05
Study Completion Date2025-03

Study Record Updates

Study Start Date2022-07-05
Study Completion Date2025-03

Terms related to this study

Additional Relevant MeSH Terms

  • Rheumatoid Arthritis