Charlottesville, VANCT07524244Now EnrollingIRB Ready

Rheumatoid Arthritis (RA) Clinical Trial in Charlottesville, VA

Access cutting-edge rheumatoid arthritis (ra) treatment through this clinical trial at a research site in Charlottesville. Study-provided care at no cost to qualified participants.

Sponsored by Fuller Research Foundation

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Expert Care in Charlottesville

Access rheumatoid arthritis (ra) specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related rheumatoid arthritis (ra) treatment provided free

Apply for This Charlottesville Location

Check if you qualify for this rheumatoid arthritis (ra) clinical trial in Charlottesville, VA

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Charlottesville

    Convenient for VA residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Charlottesville site if eligible
  4. 4Begin participation

About This Rheumatoid Arthritis (RA) Study in Charlottesville

This study is a randomized controlled clinical trial evaluating whether two therapeutic dietary approaches - a ketogenic diet and a carnivore (lion) diet - can improve quality of life, reduce symptoms, and influence measures of disease activity in adults with inflammatory bowel disease \[ulcerative colitis and Crohn's disease\] (IBD) or rheumatoid arthritis (RA). Participants will be randomized into one of three groups: 1) Ketogenic Diet, 2) Carnivore (Lion) Diet or 3) Wait-List Control. Participants randomized to a dietary group (ketogenic diet or carnivore diet) will be provided guidance on their specific dietary therapy and answer questions about their symptoms and quality of life at different intervals over a 24 week period. Participants will also complete laboratory testing at different intervals to assess for changes in nutritional status, cardiometabolic health and markers of immune activation and inflammation. Participants initially placed on the wait-list group will be asked similar questions about their symptoms and quality of life and complete the same laboratory testing as participants in a dietary group. Participants on the wait list will then be compared to participants following a specific dietary pattern to assess for any differences between the 2 groups. After 12 weeks, participants on the wait list will be randomized to a dietary group (ketogenic diet or carnivore diet) and followed in a similar fashion for an additional 12 week period.

Sponsor: Fuller Research Foundation

Who Can Participate

Inclusion Criteria

Diagnosed with medically verifiable IBD or medically verifiable RA
Current personal residence in the continental U.S.
Willingness and ability to follow dietary protocols

Exclusion Criteria

Inability to provide consent
Individuals with Type 1 or Type II Diabetes on prescription medications including insulin
Outside of the age or BMI criteria
No medically definitive or verifiable diagnosis of IBD or RA
History of strictures or fistula (IBD)
History of blood transfusion in the previous 6 months
6 months Postpartum
Breastfeeding
On other medications outside of FDA approved medications
Current initiation of disease modifying or biologic medication within the past 2 months
Unable to complete, for any reason, the initial 3-week run-in period prior to the beginning of the formal study intervention
Non-English Speaking
Organ failure of any kind including heart, liver and kidney failure or disease
History of malignancy within the last year prior to enrollment
Red meat allergy, alpha-gal allergy

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Charlottesville?

Yes, this clinical trial (NCT07524244) has an active research site in Charlottesville, VA that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Rheumatoid Arthritis (RA) Treatment Options in Charlottesville, VA

If you're searching for rheumatoid arthritis (ra) treatment options in Charlottesville, VA, this clinical trial (NCT07524244) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Charlottesville research site is actively enrolling participants for this clinical trial. You'll receive care from experienced rheumatoid arthritis (ra) specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all rheumatoid arthritis (ra) clinical trials near you to find additional studies recruiting in your area.

More Rheumatoid Arthritis Trials in Charlottesville, VA

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