Oxidative Stress in Autoimmune Rheumatic Diseases (REDOX-ARD)
Investigation of the Role of Redox Status of Patients With Autoimmune Rheumatic Diseases on Disease Progression: An Epidemiological Study
Study Overview
Status
Status
Conditions
Conditions
Detailed Description
Study Type
Study Type
Enrollment (Estimated)
Enrollment
Contacts and Locations
Study Locations
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Thessaly
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Larissa, Thessaly, Greece
- Recruiting
- General University Hospital of Larissa. Greece
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Contact:
- Karaventza Marianthi
- Phone Number: 0030 6972758418
- Email: markaraventza@gmail.com
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Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Adult patients (>18 years old), with a primary diagnosis of rheumatoid arthritis using the criteria of American College of Rheumatology (ACR)
- Adult patients (>18 years old), with a primary diagnosis of psoriatic arthritis using the ClASsification criteria for Psoriatic Arthritis (CASPAR)
- Adult patients (>18 years old), with a primary diagnosis of alkylosing spondyloarthritis using the criteria of Assessment of SpondyloArthritis international Society (ASAS) group
- Adult patients (>18 years old) irrespective of gender
- Adult patients (>18 years old) irrespective of ethnicity
- Adult patients (>18 years old) irrespective of comorbidities
- Adult patients (>18 years old) irrespective of socioeconomic background
- Adult patients (>18 years old) with any disease status
- Adult patients (>18 years old) with any disease duration
- Adult patients (>18 years old) under any treatment scheme (e.g. non-steroidal anti-inflammatory drugs, steroids, disease-modifying anti-rheumatic drugs including biologics)
Exclusion Criteria:
- Adult patients (>18 years old) with concurrent infectious disease
- Adult patients (>18 years old) in pregnancy
- Patients under 18 years of age
Study Plan
How is the study designed?
Design Details
Number of groups / cohorts
Cohorts and Interventions
Group / CohortGroup / Cohort |
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Patients with rheumatoid arthritis
No intervention
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Patients with psoriatic arthritis
No intervention
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Patients with ankylosing spondylitis
No intervention
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Patients with systemic lupus erythematosus
No intervention
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Patients with scleroderma
No intervention
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What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Concentration of blood reduced glutathione (GSH)
Time Frame: GSH concentration will compared between Day 1 and Days 180 and 360
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The concentration of reduced form of glutathione (GSH) as a crucial intrinsic antioxidant metabolite will be measured spectrophotometrically in erythrocytes.
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GSH concentration will compared between Day 1 and Days 180 and 360
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Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Concentration of protein carbonyls in blood
Time Frame: Protein carbonyl concentration will compared between Day 1 and Days 180 and 360
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The concentration of protein carbonyls, as a biomarker of protein oxidation, will be evaluated spectrophotometrically in plasma.
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Protein carbonyl concentration will compared between Day 1 and Days 180 and 360
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Total antioxidant capacity (TAC) of blood
Time Frame: TAC will be compared between Day 1 and Days 180 and 360
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TAC is a crude biomarker of antioxidant capacity of blood
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TAC will be compared between Day 1 and Days 180 and 360
|
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Activity of erythrocyte catalase
Time Frame: Catalase activity will be compared between Day 1 and Days 180 and 360
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Catalase is a primary antioxidant enzyme
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Catalase activity will be compared between Day 1 and Days 180 and 360
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Concentration of C-reactive protein (CRP) in blood
Time Frame: CRP conentration will be compared between Day 1 and Days 180 and 360
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CRP is an established biomarker of acute inflammation
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CRP conentration will be compared between Day 1 and Days 180 and 360
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Erythrocyte sedimentation rate
Time Frame: Erythrocyte sedimentation rate will be compared between Day 1 and Days 180 and 360]
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Erythrocyte sedimentation rate is an index of inflammation
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Erythrocyte sedimentation rate will be compared between Day 1 and Days 180 and 360]
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Severity of rheumatoid arthritis
Time Frame: Data of DAS28 will be compared between Day 1 and Days 180 and 360
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It will be evaluated with the disease activity score 28 (DAS28).
It combines 4 components, namely tender joint count, swollen joint count, inflammation and patient global assessment with a 0-100 VAS scale (0 = very good, 100 = very bad).
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Data of DAS28 will be compared between Day 1 and Days 180 and 360
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Severity of psoriatic arthritis
Time Frame: Data of PASI will be compared between Day 1 and Days 180 and 360
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It will be evaluated with the psoriasis area and severity Index (PASI).
It combines 2 components, namely, severity of skin lesions and area of skin affected.
Higher final score implies more severe symptoms.
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Data of PASI will be compared between Day 1 and Days 180 and 360
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Severity of alkylosing spondyloarthritis
Time Frame: Data of SLEDAI will be compared between Day 1 and Days 180 and 360
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It will be evaluated with the SLE disease activity index (SLEDAI).
It assesses clinical manifestations and laboratory findings in a scale 1 (less severe) - 8 (more severe).
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Data of SLEDAI will be compared between Day 1 and Days 180 and 360
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Physical activity levels
Time Frame: Physical activity levels will be compared between Day 1 and Days 180 and 360
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It will be measured through the international physical activity questionnaire (IPAC).
Data for minutes of vigorous activity, moderate activity, walking and sitting time is collected.
According to the obtained mean exercise time, physical activity levels are considered as high, moderate or low.
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Physical activity levels will be compared between Day 1 and Days 180 and 360
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Health status
Time Frame: Health status will be compared between Day 1 and Days 180 and 360
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Health status will be evaluated through the health assessment questionnaire
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Health status will be compared between Day 1 and Days 180 and 360
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Fatigue levels
Time Frame: Fatigue levels will be compared between Day 1 and Days 180 and 360
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It will be measured through the fatigue severity scale (FSS).
FSS is a 9-item, self-administered questionnaire which assesses the magnitude of fatigue that the volunteers have experienced throughout the past weeks.
Each item is scored on a 7-point Likert scale ranging from 1 (i.e., completely disagree) to 7 (i.e., completely agree).
High values = more severe fatigue.
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Fatigue levels will be compared between Day 1 and Days 180 and 360
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Sleep quality
Time Frame: Sleep quality levels will be compared between Day 1 and Days 180 and 360
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It will be measured through the Pittsburgh sleep quality index (PSQI).
PSQI is a 19-item self-reported questionnaire, which assesses sleep quality and quantity, sleep habits related to quality and occurrence of sleep disturbances consisting of 7 components.
Each component score is marked on a 0-3 scale, and the PSQI is calculated as the sum of the 7 components ranging between 0 and 21.
Higher final score = better sleep quality.
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Sleep quality levels will be compared between Day 1 and Days 180 and 360
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Nutritional habits
Time Frame: Nutritional habits will be compared between Day 1 and Days 180 and 360
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Nutritional habits will be recorded through an one-day recall diary
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Nutritional habits will be compared between Day 1 and Days 180 and 360
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Demographic data
Time Frame: Demographic data will be compared between Day 1 and Days 180 and 360
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Body mass index, smoking, alcohol consumption, place of residence, health insurance, educational status, family status and financial status will be collected among others through a questionnaire.
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Demographic data will be compared between Day 1 and Days 180 and 360
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Quality of life
Time Frame: The measured parameters of the quality of life of the volunteers will be compared between Day 1 and Days 180 and 360
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It will be measured through the SF-36 questionnaire.
This instrument has a physical component and a mental component.
In particular, SF-36 assesses the following health parameters of the participants: Physical functioning, Role limitations due to physical health, Bodily pain, General health perceptions, Vitality, Social functioning, Role limitations due to emotional problems and Mental health.
Each domain is scored from 0 to 100.
Higher score = better health or better quality of life.
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The measured parameters of the quality of life of the volunteers will be compared between Day 1 and Days 180 and 360
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Collaborators and Investigators
Sponsor
Sponsor
Collaborators
Collaborators
Publications and helpful links
General Publications
- Phull AR, Nasir B, Haq IU, Kim SJ. 2018. Oxidative stress, consequences and ROS mediated cellular signaling in rheumatoid arthritis. Chemico-biological interactions, 281, 7, 121-136.
- Nitschke E, Gottesman K, Hamlett P, Mattar L, Robinson J, Tovar A, Rozga M. 2022. Impact of Nutrition and Physical Activity Interventions Provided by Nutrition and Exercise Practitioners for the Adult General Population: A Systematic Review and Meta-Analysis. Nutrients, 14(9): 1729.
- World Health Organization Physical Activity 2022β. Available online: https://www.who.int/news-room/fact-sheets/detail/physical-activity.
- World Health Organization Noncommunicable Diseases 2022α. Available online: https://www.who.int/news-room/fact-sheets/detail/noncommunicable-diseases.
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Estimated)
Primary Completion
Study Completion (Estimated)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Axial Spondyloarthritis
- Bone Diseases
- Musculoskeletal Diseases
- Arthritis
- Joint Diseases
- Rheumatic Diseases
- Connective Tissue Diseases
- Autoimmune Diseases
- Immune System Diseases
- Spinal Diseases
- Spondylarthropathies
- Ankylosis
- Skin Diseases, Papulosquamous
- Skin Diseases
- Spondylarthritis
- Spondylitis
- Psoriasis
- Skin and Connective Tissue Diseases
- Spondylitis, Ankylosing
- Arthritis, Rheumatoid
- Arthritis, Psoriatic
Other Study ID Numbers
Other Study ID Numbers
- 72/8.01.2025
- 42339/17/10/2024 (Other Identifier: Scientific Board of the General University Hospital of Larissa, Greece)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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