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Effects of an Intervention With EVOO and Physical Activity in Patients With Systemic Lupus Erythematosus (EFINUTRILES)

Primary Purpose

Lupus Erythematosus, Systemic

Status
Recruiting
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Extra Virgin Olive Oil (EVOO)
Physical Exercise Program
Sponsored by
Universidad de Granada
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Lupus Erythematosus, Systemic focused on measuring Mediterranean Diet, Olive Oil, Physical Exercise, Autoimmune Diseases, Systemic Lupus Erythematosus, Microbiome, Epigenetcis

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Patients will be eligible if they have been diagnosed with SLE for at least one year and have been seen at the Outpatient Clinic of the Systemic Autoimmune Diseases Unit of the Hospital Universitario Clínico San Cecilio of Granada (Spain), meet the revised American College of Rheumatology (ACR), SLICC or ACR/EULAR criteria of 2019 and maintain a stable SLEDAI-2K, without treatment modifications, in the previous 3 months.

Inclusion Criteria:

  • Medium (8 to 11 points) to high (12 to 14 points) level of adherence to DM as measured by the 14-point DM adherence scale of the PREDIMED study.
  • Sedentary, inactive or non-performing subjects of structured PE (+5h sitting or doing less than 300min of weekly physical activity or <60min structured exercise per week).

Exclusion Criteria:

  • Terminal stages of the disease
  • Serum creatinine levels ≥1.5mg / dl
  • Type 1 Diabetes Mellitus
  • Infection, trauma or surgery six months prior to intervention
  • SLICC> 5
  • Pregnant, with intention, or breastfeeding
  • Diagnosis of other autoimmune / inflammatory diseases
  • Participation in other PE guided programs
  • Contraindication for PE: psychiatric or cognitive disorders, acute or chronic conditions (advanced lung disease, high requirements, stenosis> 70%)
  • BMI of morbid obesity (≥40)

Sites / Locations

  • Universidad de GranadaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

No Intervention

Experimental

Experimental

Arm Label

Control Group

Oil Group

Oil + Exercise Group

Arm Description

Control Group with 30 patients diagnosed with SLE following their normal lifestyle in terms of dietary intake and physical exercise.

Group with 30 patients diagnosed with SLE that add to their normal dietary intake a supplementation with 40ml of EVOO daily during 24 weeks, without changing their lifestyle in terms of physical exercise.

Group with 30 patients diagnosed with SLE that besides adding to their normal dietary intake a supplementation with 40ml of EVOO daily during 24 weeks, will follow a physical exercise multimodal program the 12 last weeks.

Outcomes

Primary Outcome Measures

SLEDAI Systemic Lupus Erythematosus Disease Activity Index
SLE-specific index that assess disease activity through a combination of data from clinical records, physical examination, organ-specific functional tests and serological studies.

Secondary Outcome Measures

Cumulative manifestations
All the manifestations and complications that patients go through or appear during the intervention, recorded by interview with clinicians.
SLICC/ACR (Systemic Lupus International Collaborating clinics/American College of Rheumatology) Damage Index for Systemic Lupus Erythematosus.
Index developed to quantify damage that has occurred since onset of lupus, correlates with mortality. Score and clinical relevance registered by interview with clinicians.
Pharmacological prescription
All the medicines that the patients are taking, start to take, o stop taking during the intervention, registered by interview with clinicians.
Glucose level
Glucose will be analyzed through blood test.
Urea level
Urea will be analyzed through blood test.
Creatinine level
Creatinine will be analyzed through blood test.
Lipid profile analysis
Lipid profile will be analyzed through blood test.
Creatine Kinase concentration
Creatine Kinase (CK) will be analyzed through blood test.
Hemoglobin concentration
Hemoglobin (Hb) will be analyzed through blood test.
Number of lymphocytes
Number of lymphocytes will be analyzed through blood test.
Number of platelets
Number of platelets will be analyzed through blood test.
Number of leukocytes
Number of leukocytes will be analyzed through blood test.
Inflammation
C-Reactive Protein (CRP) will be analyzed trough blood test.
Anti phospholipid antibodies concentration
Autoimmunity Anti phospholipid antibodies parameter will be analyzed through blood test.
Double-stranded anti-DNA antibodies concentration
Autoimmunity Double-stranded anti-DNA antibodies parameter will be analyzed through blood test.
Complement fraction C3 concentration
Autoimmunity Complement fraction C3 parameter will be analyzed through blood test.
Complement fraction C4 concentration
Autoimmunity Complement fraction C4 parameter will be analyzed through blood test.
Cardiorespiratory Fitness
Evaluated by Treadmill Ergometric test.
Functional capacity
Evaluated by the 6-Minute walking test.
Hight
In centimeters; will be evaluated using a measuring tape.
Weight
In kilograms; will be evaluated using an Inbody.
Skeletal Muscle Mass
In kilograms; will be evaluated using an Inbody.
Body Fat Mass
In kilograms; will be evaluated using an Inbody.
Body Mass Index
Weight and height will be combined to report Body Mass Index (BMI) in kg/m^2
Body Fat Index
In %; will be evaluated using an Inbody.
Waist-to-hip ratio in centimeters
In centimeters; waist circumference and hip circumference measures will be combined to calculate waist-to-hip ratio (WHR).
Obesity degree
In %; will be evaluated using an Inbody.
Body Cell Mass
In kilograms; will be evaluated using an Inbody.
Bone Mineral Content
In kilograms; will be evaluated using an Inbody.
Basal Metabolic Rate
In kilocalories; will be evaluated using an Inbody.
Visceral Fat Area
In cm^2; Visceral Fat Area (AVG) will be evaluated using an Inbody.
Bone density
Evaluated by densitometry.
Human Vascular Cell Adhesion Molecule-1 concentration
VCAM-1 endothelial biomarker will be assessed by blood test.
Intercellular Adhesion Molecule-1concentration
ICAM-1 endothelial biomarker will be assessed by blood test.
E-Selectin concentration
E-Selectin endothelial biomarker will be assessed by blood test.
Super Oxide Dismutase concentration
Oxidative Stress SOD biomarker will be assessed by blood test.
Glutathione concentration
Oxidative Stress GSH biomarker will be assessed by blood test.
Total Antioxidant Capacity concentration
Oxidative Stress TAC biomarker will be assessed by blood test.
Thiobarbituric Acid Reactive Substances concentration
Oxidative Stress TBARS biomarker will be assessed by blood test.
Malondialdehyde concentration
Oxidative Stress MDA biomarker will be assessed by blood test.
Advanced Oxidation Protein Products concentration
Oxidative Stress AOPP biomarker will be assessed by blood test.
Total proteins concentration
Oxidative Stress total proteins biomarker, understood as the concentration of proteins in a sample, will be assessed by blood test.
Endothelial Function
Several endothelial function parameters such are arterial pulse wave velocity, AIX index, ABI will be evaluated using arteriography.
miRNA expression profile quantification
Collection of blood samples in Tempus tubes for subsequent analysis of miRNA expression profile by massive sequencing with specific equipment.
Microbiome characteristics analysis
Microbiome study by collecting fecal samples.

Full Information

First Posted
February 8, 2022
Last Updated
December 19, 2022
Sponsor
Universidad de Granada
Collaborators
Consejería de Economía, Innovación y Ciencia. Proyectos de I+D+I en el marco operativo Feder Andalucía 2014-2020
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1. Study Identification

Unique Protocol Identification Number
NCT05261529
Brief Title
Effects of an Intervention With EVOO and Physical Activity in Patients With Systemic Lupus Erythematosus
Acronym
EFINUTRILES
Official Title
Effects of a Nutricional Intervention With EVOO Oil and Physical Activity in Patients With Systemic Lupus Erythematosus: Effect on Clinical Course, Epigenetic and Microbiome
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Recruiting
Study Start Date
November 3, 2021 (Actual)
Primary Completion Date
December 30, 2022 (Anticipated)
Study Completion Date
June 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universidad de Granada
Collaborators
Consejería de Economía, Innovación y Ciencia. Proyectos de I+D+I en el marco operativo Feder Andalucía 2014-2020

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
In addition to the different pharmacological therapies available for the treatment of Systemic Lupus Erythematosus (SLE) as well as for its numerous associated complications (cutaneous, articular, hematological, neuropsychiatric, renal...), it has recently been proposed that 'health-related lifestyles' could have a determining role in balancing numerous organic processes at all levels. In line with this, the benefits of following a healthy dietary pattern such as the Mediterranean Diet and, specifically, the intake of Extra Virgin Olive Oil (EVOO) as well as the realization of regular physical exercise (PE) have been examined in numerous chronic non-communicable diseases such as obesity or cancer. However, in patients with autoimmune diseases, such as SLE, the possible effects of this synergy has not been investigated to date. Having demonstrated both the protective effect of a healthy dietary pattern and that of regular PE on the progression and risks associated with SLE in cross-sectional studies, non-intervention research has been developed that combines both strategies simultaneously, with nutritional supplementation or PE occurring independently. It is hypothesized that supplementation with EVOO in these patients together with PE will produce superior benefits compared to EVOO supplementation alone, showing changes in the phenotype of SLE and other parameters such as levels of chronicity/gravity, biomarkers (oxidative stress, immunological, inflammation), cardiovascular status and body composition.
Detailed Description
SLE is one of the more representative autoimmune diseases that courses with several manifestations which are cutaneous-mucosal, joint, hematologic, neuropsychiatric and/or renal. In addition to the different pharmacological therapies available for its treatment, the adequate management of 'health-related lifestyles' becomes a relevant strategy by balancing, among others, the dysbiosis of the microbiota, the production of metabolites and the alteration of the immune response, with positive repercussions on all organic processes. Mediterranean Diet (MD), and the intake of EVOO in specific, which is its most representative food, has been shown to be a proven dietary pattern of protection against chronic non-communicable diseases. In line with this, Physical Exercise (PE) is another strategy on the rise. Regular exercise at moderate intensity has great impact on the immune system, the central nervous system, as a regulator of hormones and blood glucose levels, and on the psychosocial and cognitive spheres, ultimately leading to the appearance of numerous beneficial modifications in the face of external pathogenic aggressions and inflammatory processes. Therefore, the synergy between DM and PE could enhance the known beneficial effects of both types of approaches in patients with SLE, as the scientific literature has shown in other chronic diseases such as obesity or cancer, among others. However, there are currently few studies that include PE interventions, and there is also some contradiction in the results. In addition, there is no study that synergizes both approaches in a coincident manner over time. The present study, whose main objective is to analyze the influence of the addition to a supplementation with EVOO of a multimodal combined physical exercise intervention in patients with SLE, is developed under the hypothesis that: The combination of dietary supplementation with EVOO together with the follow-up of a multimodal PE program will result in superior benefits in SLE patients with respect to a group of patients solely supplemented with EVOO, showing changes in SLE phenotype and parameters such as levels of chronicity/severity of the disease, levels of biochemical, immunological, inflammatory and oxidative stress markers, markers of cardiovascular risk and early atherosclerosis and endothelial function, cardiorespiratory status and body composition. For this purpose, a 24-week clinical trial will be developed with three groups of patients with SLE (30 patients/group): a control group (no intervention), another that will add to the usual intake pattern of 40ml of EVOO daily during 24 weeks, and a third group that will add to this additional intake of EVOO the follow-up of a specific PE program in the middle of the intervention (12 weeks). Data collection in all groups will be perform before the intervention, at an intermediate stage and coinciding with the beginning of the PE program (12 weeks), and at the end of the study (24 weeks). The study will be carried out in three phases: STAGE 1: Reinforcement of adherence to DM. In order to guarantee during the intervention the maintenance of the levels of adherence to DM established as inclusion criteria, previously and in both groups the basic principles of DM will be recalled by a nutritionist, through group sessions of 1 hour of duration. STAGE 2: Intervention. EVOO supplementation, or EVOO supplementation + PE under the conditions previously described. The intervention, which will be extended over 24 weeks, will consist of the daily consumption of 40 ml of EVOO in a single daily intake, added to the usual intake pattern of the participants. CG. The participants' usual lifestyle (dietary pattern and physical activity) will not be modified. Intervention Group 1. Patients will take the EVOO supplementation as describe below, without changing their physical activity routines. Intervention Group 2. In addition to taking EVOO supplementation, patients will start following a Multimodal Physical Exercise (MFE) program during the remaining 12 weeks of intervention, guided by personnel with experience in the area: 3 days per week, groupal sessions (≤10 participants/group) on non-consecutive days, both online and face-to-face sessions. Continuous (4-6weeks) and intervallic (week 5-7 to 24) cardiovascular exercise will be worked at moderate-intense intensity, controlled by HR in reserve, with a duration of 15-45 minutes. In addition, sympathetic modulation exercises (stretching, breathing, meditation) will be used as methods to promote recovery, with a duration of 10-30 minutes. In this group, supplementation will take place after exertion. STAGE 3: Post-intervention data collection (week 25).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lupus Erythematosus, Systemic
Keywords
Mediterranean Diet, Olive Oil, Physical Exercise, Autoimmune Diseases, Systemic Lupus Erythematosus, Microbiome, Epigenetcis

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Three-arm prospective randomized controlled 24-week clinical trial of patients diagnosed with SLE.
Masking
InvestigatorOutcomes Assessor
Masking Description
Participants randomly assigned in a 1:1:1 ratio to each of the three groups established through a centralized method with computer support (OxMaR software).
Allocation
Randomized
Enrollment
90 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control Group
Arm Type
No Intervention
Arm Description
Control Group with 30 patients diagnosed with SLE following their normal lifestyle in terms of dietary intake and physical exercise.
Arm Title
Oil Group
Arm Type
Experimental
Arm Description
Group with 30 patients diagnosed with SLE that add to their normal dietary intake a supplementation with 40ml of EVOO daily during 24 weeks, without changing their lifestyle in terms of physical exercise.
Arm Title
Oil + Exercise Group
Arm Type
Experimental
Arm Description
Group with 30 patients diagnosed with SLE that besides adding to their normal dietary intake a supplementation with 40ml of EVOO daily during 24 weeks, will follow a physical exercise multimodal program the 12 last weeks.
Intervention Type
Dietary Supplement
Intervention Name(s)
Extra Virgin Olive Oil (EVOO)
Intervention Description
Daily intake of 40ml EVOO added to the normal intake of EVOO of the participants.
Intervention Type
Behavioral
Intervention Name(s)
Physical Exercise Program
Intervention Description
Besides the EVOO supplementation in the same conditions as the 'Intervention 1 Group', participants will add the follow-up of a Multimodal Physical Exercise (MFE) program during the remaining 12 weeks of intervention, 3 days per week, online and face-to-face group sessions on non-consecutive days. Continuous and intervalic cardiovascular exercise at moderate-intense intensity, controlled by the HR in reserve, with a duration of 15-45 minutes, also including sympathetic modulation exercises (stretching, breathing and meditation) and methods to promote recovery, with a duration of 10-30 minutes.
Primary Outcome Measure Information:
Title
SLEDAI Systemic Lupus Erythematosus Disease Activity Index
Description
SLE-specific index that assess disease activity through a combination of data from clinical records, physical examination, organ-specific functional tests and serological studies.
Time Frame
Participants will be followed over 24 weeks.
Secondary Outcome Measure Information:
Title
Cumulative manifestations
Description
All the manifestations and complications that patients go through or appear during the intervention, recorded by interview with clinicians.
Time Frame
Participants will be followed over 24 weeks.
Title
SLICC/ACR (Systemic Lupus International Collaborating clinics/American College of Rheumatology) Damage Index for Systemic Lupus Erythematosus.
Description
Index developed to quantify damage that has occurred since onset of lupus, correlates with mortality. Score and clinical relevance registered by interview with clinicians.
Time Frame
Participants will be followed over 24 weeks.
Title
Pharmacological prescription
Description
All the medicines that the patients are taking, start to take, o stop taking during the intervention, registered by interview with clinicians.
Time Frame
Participants will be followed over 24 weeks.
Title
Glucose level
Description
Glucose will be analyzed through blood test.
Time Frame
Participants will be followed over 24 weeks.
Title
Urea level
Description
Urea will be analyzed through blood test.
Time Frame
Participants will be followed over 24 weeks.
Title
Creatinine level
Description
Creatinine will be analyzed through blood test.
Time Frame
Participants will be followed over 24 weeks.
Title
Lipid profile analysis
Description
Lipid profile will be analyzed through blood test.
Time Frame
Participants will be followed over 24 weeks.
Title
Creatine Kinase concentration
Description
Creatine Kinase (CK) will be analyzed through blood test.
Time Frame
Participants will be followed over 24 weeks.
Title
Hemoglobin concentration
Description
Hemoglobin (Hb) will be analyzed through blood test.
Time Frame
Participants will be followed over 24 weeks.
Title
Number of lymphocytes
Description
Number of lymphocytes will be analyzed through blood test.
Time Frame
Participants will be followed over 24 weeks.
Title
Number of platelets
Description
Number of platelets will be analyzed through blood test.
Time Frame
Participants will be followed over 24 weeks.
Title
Number of leukocytes
Description
Number of leukocytes will be analyzed through blood test.
Time Frame
Participants will be followed over 24 weeks.
Title
Inflammation
Description
C-Reactive Protein (CRP) will be analyzed trough blood test.
Time Frame
Participants will be followed over 24 weeks.
Title
Anti phospholipid antibodies concentration
Description
Autoimmunity Anti phospholipid antibodies parameter will be analyzed through blood test.
Time Frame
Participants will be followed over 24 weeks.
Title
Double-stranded anti-DNA antibodies concentration
Description
Autoimmunity Double-stranded anti-DNA antibodies parameter will be analyzed through blood test.
Time Frame
Participants will be followed over 24 weeks.
Title
Complement fraction C3 concentration
Description
Autoimmunity Complement fraction C3 parameter will be analyzed through blood test.
Time Frame
Participants will be followed over 24 weeks.
Title
Complement fraction C4 concentration
Description
Autoimmunity Complement fraction C4 parameter will be analyzed through blood test.
Time Frame
Participants will be followed over 24 weeks.
Title
Cardiorespiratory Fitness
Description
Evaluated by Treadmill Ergometric test.
Time Frame
Participants will be followed over 24 weeks.
Title
Functional capacity
Description
Evaluated by the 6-Minute walking test.
Time Frame
Participants will be followed over 24 weeks.
Title
Hight
Description
In centimeters; will be evaluated using a measuring tape.
Time Frame
Participants will be followed over 24 weeks.
Title
Weight
Description
In kilograms; will be evaluated using an Inbody.
Time Frame
Participants will be followed over 24 weeks.
Title
Skeletal Muscle Mass
Description
In kilograms; will be evaluated using an Inbody.
Time Frame
Participants will be followed over 24 weeks.
Title
Body Fat Mass
Description
In kilograms; will be evaluated using an Inbody.
Time Frame
Participants will be followed over 24 weeks.
Title
Body Mass Index
Description
Weight and height will be combined to report Body Mass Index (BMI) in kg/m^2
Time Frame
Participants will be followed over 24 weeks.
Title
Body Fat Index
Description
In %; will be evaluated using an Inbody.
Time Frame
Participants will be followed over 24 weeks.
Title
Waist-to-hip ratio in centimeters
Description
In centimeters; waist circumference and hip circumference measures will be combined to calculate waist-to-hip ratio (WHR).
Time Frame
Participants will be followed over 24 weeks.
Title
Obesity degree
Description
In %; will be evaluated using an Inbody.
Time Frame
Participants will be followed over 24 weeks.
Title
Body Cell Mass
Description
In kilograms; will be evaluated using an Inbody.
Time Frame
Participants will be followed over 24 weeks.
Title
Bone Mineral Content
Description
In kilograms; will be evaluated using an Inbody.
Time Frame
Participants will be followed over 24 weeks.
Title
Basal Metabolic Rate
Description
In kilocalories; will be evaluated using an Inbody.
Time Frame
Participants will be followed over 24 weeks.
Title
Visceral Fat Area
Description
In cm^2; Visceral Fat Area (AVG) will be evaluated using an Inbody.
Time Frame
Participants will be followed over 24 weeks.
Title
Bone density
Description
Evaluated by densitometry.
Time Frame
Participants will be followed over 24 weeks.
Title
Human Vascular Cell Adhesion Molecule-1 concentration
Description
VCAM-1 endothelial biomarker will be assessed by blood test.
Time Frame
Participants will be followed over 24 weeks.
Title
Intercellular Adhesion Molecule-1concentration
Description
ICAM-1 endothelial biomarker will be assessed by blood test.
Time Frame
Participants will be followed over 24 weeks.
Title
E-Selectin concentration
Description
E-Selectin endothelial biomarker will be assessed by blood test.
Time Frame
Participants will be followed over 24 weeks.
Title
Super Oxide Dismutase concentration
Description
Oxidative Stress SOD biomarker will be assessed by blood test.
Time Frame
Participants will be followed over 24 weeks.
Title
Glutathione concentration
Description
Oxidative Stress GSH biomarker will be assessed by blood test.
Time Frame
Participants will be followed over 24 weeks.
Title
Total Antioxidant Capacity concentration
Description
Oxidative Stress TAC biomarker will be assessed by blood test.
Time Frame
Participants will be followed over 24 weeks.
Title
Thiobarbituric Acid Reactive Substances concentration
Description
Oxidative Stress TBARS biomarker will be assessed by blood test.
Time Frame
Participants will be followed over 24 weeks.
Title
Malondialdehyde concentration
Description
Oxidative Stress MDA biomarker will be assessed by blood test.
Time Frame
Participants will be followed over 24 weeks.
Title
Advanced Oxidation Protein Products concentration
Description
Oxidative Stress AOPP biomarker will be assessed by blood test.
Time Frame
Participants will be followed over 24 weeks.
Title
Total proteins concentration
Description
Oxidative Stress total proteins biomarker, understood as the concentration of proteins in a sample, will be assessed by blood test.
Time Frame
Participants will be followed over 24 weeks.
Title
Endothelial Function
Description
Several endothelial function parameters such are arterial pulse wave velocity, AIX index, ABI will be evaluated using arteriography.
Time Frame
Participants will be followed over 24 weeks.
Title
miRNA expression profile quantification
Description
Collection of blood samples in Tempus tubes for subsequent analysis of miRNA expression profile by massive sequencing with specific equipment.
Time Frame
Participants will be followed over 24 weeks.
Title
Microbiome characteristics analysis
Description
Microbiome study by collecting fecal samples.
Time Frame
Participants will be followed over 24 weeks.

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Patients will be eligible if they have been diagnosed with SLE for at least one year and have been seen at the Outpatient Clinic of the Systemic Autoimmune Diseases Unit of the Hospital Universitario Clínico San Cecilio of Granada (Spain), meet the revised American College of Rheumatology (ACR), SLICC or ACR/EULAR criteria of 2019 and maintain a stable SLEDAI-2K, without treatment modifications, in the previous 3 months. Inclusion Criteria: Medium (8 to 11 points) to high (12 to 14 points) level of adherence to DM as measured by the 14-point DM adherence scale of the PREDIMED study. Sedentary, inactive or non-performing subjects of structured PE (+5h sitting or doing less than 300min of weekly physical activity or <60min structured exercise per week). Exclusion Criteria: Terminal stages of the disease Serum creatinine levels ≥1.5mg / dl Type 1 Diabetes Mellitus Infection, trauma or surgery six months prior to intervention SLICC> 5 Pregnant, with intention, or breastfeeding Diagnosis of other autoimmune / inflammatory diseases Participation in other PE guided programs Contraindication for PE: psychiatric or cognitive disorders, acute or chronic conditions (advanced lung disease, high requirements, stenosis> 70%) BMI of morbid obesity (≥40)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
María Corea Rodríguez, Professor
Phone
958243494
Ext
+34
Email
macoro@ugr.es
First Name & Middle Initial & Last Name or Official Title & Degree
Blanca M Rueda Medina, Professor
Phone
958243494
Ext
+34
Email
blarume@ugr.es
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
María Correa Rodríguez, Professor
Organizational Affiliation
Universidad de Granada
Official's Role
Principal Investigator
Facility Information:
Facility Name
Universidad de Granada
City
Granada
State/Province
Granada, Spain
ZIP/Postal Code
18016
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
María Correa Rodríguez, Professor
Phone
958243494
Ext
+34
Email
macoro@ugr.es
First Name & Middle Initial & Last Name & Degree
Blanca M Rueda Medina, Professor
Phone
958243494
Ext
+34
Email
blarume@ugr.es
First Name & Middle Initial & Last Name & Degree
Blanca M Rueda Medina, Professor
First Name & Middle Initial & Last Name & Degree
María Correa Rodríguez, Professor
First Name & Middle Initial & Last Name & Degree
Norberto Ortego Centeno, Professor
First Name & Middle Initial & Last Name & Degree
Jose L Callejas Rubio, Clinician
First Name & Middle Initial & Last Name & Degree
Raquel Ríos Fernández, Clinician
First Name & Middle Initial & Last Name & Degree
Julio J Gálvez Peralta, Professor
First Name & Middle Initial & Last Name & Degree
Alba Rodríguez Nogales, Assistant
First Name & Middle Initial & Last Name & Degree
Irene Cantarero Villanueva, Professor
First Name & Middle Initial & Last Name & Degree
María del Rocío Gil Gutiérrez, Predoctoral
First Name & Middle Initial & Last Name & Degree
Sara Del Olmo Romero, Predoctoral
First Name & Middle Initial & Last Name & Degree
Irene Medina Martínez, Predoctoral
First Name & Middle Initial & Last Name & Degree
Jose C Arredondo Azor, Predoctoral

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
32594173
Citation
Pocovi-Gerardino G, Correa-Rodriguez M, Callejas-Rubio JL, Rios-Fernandez R, Martin-Amada M, Cruz-Caparros MG, Rueda-Medina B, Ortego-Centeno N. Beneficial effect of Mediterranean diet on disease activity and cardiovascular risk in systemic lupus erythematosus patients: a cross-sectional study. Rheumatology (Oxford). 2021 Jan 5;60(1):160-169. doi: 10.1093/rheumatology/keaa210.
Results Reference
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Effects of an Intervention With EVOO and Physical Activity in Patients With Systemic Lupus Erythematosus

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