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Clinical Trials/NCT01544101
NCT01544101
Completed
Not Applicable

A Nutritional Intervention for Arthritis

Physicians Committee for Responsible Medicine1 site in 1 country32 target enrollmentSeptember 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Rheumatoid Arthritis
Sponsor
Physicians Committee for Responsible Medicine
Enrollment
32
Locations
1
Primary Endpoint
Pain Score
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

The purpose of the study is to assess whether, in individuals with rheumatoid arthritis, a low-fat, vegan diet improves pain and other subjective symptoms more effectively than a control supplement or a placebo. The principal measure is pain as measured by Visual Analog Scale (VAS) and disease activity as measured by number of painful swollen and tender joints, respectively. The study duration is 36 weeks.

Detailed Description

Preliminary evidence suggests that low-fat, vegetarian diets and certain nutritional supplements can help reduce pain and also reduce the need for pain medications for some people. The investigators will ask about 100 people to participate. All of them will get a low-fat, vegan diet and a nutritional supplement (mixture of omega-3 oils and vitamin E or a placebo), although some will get the diet first, and others will get the supplement first. This order in which they will get the diet and the supplement will be determined randomly, that is, by chance (like the toss of a coin). The principal measure is pain as measured by Visual Analog Scale (VAS) and disease activity as measured by number of painful swollen and tender joints, respectively. The study duration is 36 weeks.

Registry
clinicaltrials.gov
Start Date
September 2011
End Date
October 2012
Last Updated
13 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • A diagnosis of rheumatoid arthritis, as defined below.
  • A diagnosis of rheumatoid arthritis is based on 2010 ACR / EULAR Rheumatoid Arthritis Classification Criteria. Classification as "definite RA" is based on the confirmed presence of synovitis in at least 1 joint, absence of an alternative diagnosis that better explains the synovitis, and achievement of a total score of 6 or greater (of a possible 10): 24
  • Joint involvement, designating the metacarpophalangeal joints, proximal interphalangeal joints, the interphalangeal joint of the thumb, second through third metatarsophalangeal joint and wrist as small joints, and elbows, hip joints and knees as large joints:
  • Involvement of 1 large joint gives 0 points
  • Involvement of 2-10 large joints gives 1 point
  • Involvement of 1-3 small joints (with or without involvement of large joints) gives 2 points
  • Involvement of4-10 small joints (with or without involvement of large joints) gives 3 points
  • Involvement of more than 10 joints (with involvement of at least 1 small joint) gives 5 points
  • Serological parameters - including the rheumatoid factor as well as anti-citrullinated protein antibody (ACPA):
  • Negative RF and negative ACPA gives 0 points

Exclusion Criteria

  • \< 18 years of age
  • Rheumatoid arthritis for more than 6 years
  • Alcohol consumption of more than 2 drinks per day or the equivalent, episodic increased drinking (e.g., more than 2 drinks per day on weekends), or a history of alcohol abuse or dependency followed by any current use
  • Use of recreational drugs in the past 6 months (past drug use, if fully recovered, is not a criteria for exclusion)
  • Unstable medical or psychiatric illness
  • Likely to be disruptive in group sessions (as determined by research staff)
  • Already following a low-fat, vegan diet
  • Lack of English fluency
  • Inability to maintain current medication regimen
  • Inability or unwillingness to participate in all components of the study

Outcomes

Primary Outcomes

Pain Score

Time Frame: Baseline and 4 months

will be measured by visual analog scale

Disease Activity score

Time Frame: Baseline and 4 months

measured by number of painful, swollen and tender joints

Secondary Outcomes

  • Quality of Life(Baseline and 4 months)

Study Sites (1)

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