- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02028624
Lifestyle Interventions Based on the Mediterranean Diet for Patients With Rheumatoid Arthritis
Lifestyle Interventions Based on the Mediterranean Diet for Patients With Rheumatoid Arthritis: a Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The effect of various dietary regimens and nutrient supplementation on rheumatoid arthritis (RA) has been previously explored, with the majority of the evidence supporting the beneficial effect of n-3 polyunsaturated fatty acids (PUFAs), consumed mainly as fish oil supplements. However, many capsules should be taken on a daily basis (10 - 15) in order to improve health status, increasing, thus, the high drug burden these patients may encounter; inability to comply with supplementation, as depicted in drop-out rates and adverse reactions, is also of concern. On the other hand, the so far investigation of specific dietary patterns, namely elemental or vegetarian diets, revealed similar limitations regarding inability to comply, without producing clear benefit.
The last decade, a traditional dietary pattern, the Mediterranean diet, has also been investigated in patients with RA. This pattern is characterized by abundance of plant foods (fruits, mainly as typical daily desserts, vegetables, bread, other forms of cereals, beans, nuts, and seeds), olive oil as the principal source of fat, moderate amounts of dairy products (mainly cheese and yogurt), low to moderate amounts of fish and poultry, red meat in low amounts and wine consumed in moderation, normally with meals. Adherence to the Mediterranean diet has been associated with a significant reduction in total mortality and improvement in longevity, as well as with lower incidence of atherosclerosis, coronary heart disease, metabolic syndrome and biochemical markers related to insulin resistance and inflammation. In RA, in specific, it has been shown to improve objective and subjective measures. It is also worth mentioning that this type of intervention produced negligible or no adverse effects or drop-out in RA patients. However, it has been implemented in North-European populations with a background diet far away from the Mediterranean dietary habits. It would be interesting to study the effect of a Mediterranean diet-based intervention in a Mediterranean population of RA patients, evaluate their adherence and changes in subjective disease measures as well as in biochemical markers. One of the markers of interest is adiponectin, a large 30-kDa protein produced mainly by adipocytes, sharing strong homologies with TNF and the complement factor C1q. Plasma levels of adiponectin have been negatively associated with indices of obesity, insulin resistance and cardiovascular disease. However, its role in RA is still controversial with some evidence indicating a proinflammatory effect and some other suggesting antiinflammatory properties of this adipocytokine.
Aim of the present study was to evaluate the effect of different lifestyle intervention administrations, in increasing adherence to the Mediterranean diet in a group of patients with RA living in the Mediterranean basin, and, thus, in improving parameters related to subjective and objective disease markers, including plasma adiponectin concentrations.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Athens, Greece, 11521
- Euroclinic Private Hopsital
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Athens, Greece, 15773
- Laiko General Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- adults
- rheumatoid arthritis diagnosis according to the 1987 criteria of the American College of Rheumatology
- clinically non active disease, as assessed and documented by the patient's own rheumatology specialist
Exclusion Criteria:
- being on a slimming or any other special diet during the previous year, or being diagnosed with other serious medical conditions
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Face-to-face
Patients received face-to-face nutrition counseling.
|
Patients received nutrition counseling, through one-to-one sessions conducted once a month, until the 6-month evaluation.
Nutrition counseling was based on goal-setting and aimed at increasing adherence to Mediterannean diet.
|
Experimental: Telephone
Patients received telephone nutrition counseling.
|
Patients received nutrition counseling, through one-to-one sessions conducted once a month, until the 6-month evaluation.
Nutrition counseling was based on goal-setting and aimed at increasing adherence to Mediterannean diet.
|
No Intervention: Minimum Intervention
Patients in this group received no further lifestyle-related counseling and contact until the 6-month evaluation.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Age
Time Frame: baseline
|
baseline
|
Change from baseline Mediterranean Diet Score at 6 months
Time Frame: 6 months
|
6 months
|
Change from baseline Disease Activity Score (DAS28) at 6 months
Time Frame: 6 months
|
6 months
|
Change from baseline Health Assessment Questionnaire (HAQ) Score at 6 months
Time Frame: 6 months
|
6 months
|
Change from baseline Short Form-36 Health Survey (SF-36) score at 6 months
Time Frame: 6 months
|
6 months
|
Change from baseline energy intake at 6 months
Time Frame: 6 months
|
6 months
|
Change from baseline in macronutrients intake at 6 months
Time Frame: 6 months
|
6 months
|
Height
Time Frame: baseline
|
baseline
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Change from baseline body weight at 6 months
Time Frame: 6 months
|
6 months
|
Change from baseline systolic blood pressure at 6 months
Time Frame: 6 months
|
6 months
|
Change from baseline plasma adiponectin concentrations at 6 months
Time Frame: 6 months
|
6 months
|
Change from baseline plasma glucose levels at 6 months
Time Frame: 6 months
|
6 months
|
Change from baseline serum triglycerides levels at 6 months
Time Frame: 6 months
|
6 months
|
Change from baseline plasma HDL-cholesterol levels at 6 months
Time Frame: 6 months
|
6 months
|
Years of education
Time Frame: baseline
|
baseline
|
Change from baseline diastolic blood pressure at 6 months
Time Frame: 6 months
|
6 months
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Director: Mary Yannakoulia, PhD, Harokopio University
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- RASt
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