A Nutritional Intervention for Arthritis

Rheumatoid Arthritis Clinical Trial

Official title:

A Nutritional Intervention for Arthritis

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01544101
• Other study ID #: WCCR-ARTH1
• Status: Completed
• Phase: N/A
• First received: February 27, 2012
• Last updated: October 18, 2012
• Start date: September 2011
• Est. completion date: October 2012

Study information

• Verified date: October 2012
• Source: Physicians Committee for Responsible Medicine
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 32
• Est. completion date: October 2012
• Est. primary completion date: October 2012
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. 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

• Low-positive RF or low-positive ACPA gives 2 points

• High-positive RF or high-positive ACPA gives 3 points Acute phase reactants: 1 point for elevated erythrocyte sedimentation rate (ESR) or elevated C-reactive protein (CRP) value Duration of arthritis: 1 point for symptoms lasting six weeks or longer

2. Continuing or recurring pain (i.e., joint pain daily, unless on pain medication).

3. Age at least 18 years

4. Ability and willingness to participate in all components of the study

5. Willingness to be assigned to either the diet group or supplement group

6. Pain medications unchanged within last 6 weeks.

Exclusion Criteria:

1. < 18 years of age

2. Rheumatoid arthritis for more than 6 years

3. 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

4. Use of recreational drugs in the past 6 months (past drug use, if fully recovered, is not a criteria for exclusion)

5. Pregnancy

6. Unstable medical or psychiatric illness

7. Likely to be disruptive in group sessions (as determined by research staff)

8. Already following a low-fat, vegan diet

9. Lack of English fluency

10. Inability to maintain current medication regimen

11. Inability or unwillingness to participate in all components of the study

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Supportive Care

Related Conditions & MeSH terms

• Arthritis
• Arthritis, Rheumatoid
• Rheumatoid Arthritis

Intervention

Other:
• Vegan Diet
Vegan diet, which is devoid of animal products and minimal in fat

Dietary Supplement:
• dietary supplement omega3 fatty acids aand vitamins
mixture of omega3 fatty acids aand vitamins

Locations

Country	Name	City	State
United States	Physicians Committee for Responsible Medicine	Washington	District of Columbia

Sponsors (1)

Lead Sponsor	Collaborator
Physicians Committee for Responsible Medicine

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pain Score	will be measured by visual analog scale	Baseline and 4 months	No
Primary	Disease Activity score	measured by number of painful, swollen and tender joints	Baseline and 4 months	No
Secondary	Quality of Life	measured by a modified health assessment questionnaire	Baseline and 4 months	No