- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03500276
Yoga for Patients With Rheumatoid Arthritis
Impact of Yoga on Quality of Life and Markers of Inflammation in Rheumatoid Arthritis Patients
The purpose of this study is to investigate the effects of a yoga program based on "Yoga in daily life system" in patients with rheumatoid arthritis.
The investigators want to explore whether this program will improve health-related quality of life and psychological well-being in patients. In addition they want to explore its potential positive modulation of the immune system.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Rheumatoid arthritis (RA) is a chronic disabling inflammatory disease that substantially impacts health-related quality of life (HRQOL) of patients. In addition to pain, fatigue and physical disability the disease also affects psychological health. Yoga, a mind-body therapy, integrates physical exercises with relaxation and meditation. Published data suggest its beneficial effects on both physical and mental health in various chronic conditions. The true biological mechanism underlying these effects is not well known. Recent research suggests potential modulation of the immune system and inflammation-related gene expression changes.
Hypothesis: Yoga program based on Yoga in daily life system has positive impact on clinical and biologic outcomes in RA patients.
Aims: To determine the impact of a 12-week yoga program on measures of psychological distress, HRQOL, fatigue, pain, disease activity, levels of circulating inflammatory markers and pro-inflammatory gene expression.
Materials and methods: 50 RA patients, aged 18-65 years, on stable standard pharmacological treatment will be randomly assigned to a 12-week yoga intervention (based on "Yoga in daily life system") or arthritis-education control. Self-administered questionnaires will be used to assess quality of life and psychological well-being of the patients. Blood samples will be collected for measurement of inflammatory markers and expression of a set of pro-inflammatory genes. Disease activity will be assessed by DAS28CRP score. The patients will be assessed on baseline, post-treatment and at 3 months follow-up.
This research will provide information on potential efficacy of yoga program in improving physical and psychological outcomes in persons with RA and explore its influence on immunological system.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Zagreb, Croatia, 10 000
- University Hospital Dubrava
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- ACR/EULAR 2010. classification criteria for rheumatoid arthritis (RA)
- disease activity measured by DAS28CRP< 5.1
- patients on stable dose of disease-modifying antirheumatic medications,non-steroidal anti-inflammatory drugs or low-dose glucocorticoids for the last 3 months
Exclusion Criteria:
- significant co-morbidity (active malignant disease, symptomatic ischemic heart disease or heart failure, severe lung disease, uncontrolled thyroid disease, neurological disease that impairs mobility) that is more limiting than RA
- history of drug or alcohol abuse
- recent injury/ or surgery
- regular practice of yoga or similar technique in the last 6 months or currently engaged in a structured exercise program for >=2 times weekly, patients that are currently engaged in physical therapy
- pregnant or planning pregnancy
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: Yoga program
12 weeks of "Yoga in daily life practice", 2x weekly for 90 minutes including physical exercises (asanas), breathing exercises (pranayama), relaxation and meditation exercises.
|
Yoga classes will be conducted 2xweekly/ 90 minutes and consist of physical exercises (asanas), breathing exercises (pranayama), relaxation and self-enquiry meditation based on Yoga in daily life system.
|
|
Active Comparator: Arthritis-education control
12 weeks of arthritis - education classes, consisting of 1x weekly sessions for 120 minutes including lectures on arthritis and related issues followed by group discussion.
|
Arthritis-education classes will be conducted 1xweekly/ 120 minutes and led by rheumatology specialists and consist of lectures on arthritis and related issues followed by group discussion.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in health-related quality of life
Time Frame: baseline and 12 weeks
|
The Medical Outcomes Survey 36-item Short-Form Healthy Survey ( SF-36).
A 36 item generic health survey measures general health concepts through 8 domains: physical functioning, role physical, bodily pain, global health, vitality, social functioning, role emotional, mental health.
Scores 0-100, with higher scores indicating better health
|
baseline and 12 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in pro-inflammatory gene expression
Time Frame: baseline and 12 weeks
|
RT-PCR analysis of expression of a set of pro-inflammatory genes.
Changes from baseline to 12 weeks
|
baseline and 12 weeks
|
|
Change in blood levels of hs-CRP
Time Frame: baseline and 12 weeks
|
hs-CRP (mg/l) changes from baseline to 12 weeks
|
baseline and 12 weeks
|
|
Change in blood levels of hs-CRP
Time Frame: baseline and 24 weeks
|
hs-CRP (mg/l) changes from baseline to 24 weeks
|
baseline and 24 weeks
|
|
Change in pain intensity
Time Frame: baseline and 12 weeks
|
Visual analogue scale 0-10, with higher scores indicating higher pain intensity
|
baseline and 12 weeks
|
|
Change in pain intensity
Time Frame: baseline and 24 weeks
|
Visual analogue scale 0-10, with higher scores indicating higher pain intensity
|
baseline and 24 weeks
|
|
Change in perceived stress
Time Frame: baseline and 12 weeks
|
Perceived Stress Scale (PSS) consists of 10 items.
Range 0-40 points with higher scores indicating greater levels of stress
|
baseline and 12 weeks
|
|
Change in perceived stress
Time Frame: baseline and 24 weeks
|
Perceived Stress Scale (PSS) consists of 10 items.
Range 0-40 points with higher scores indicating greater levels of stress
|
baseline and 24 weeks
|
|
Change in rheumatoid arthritis activity
Time Frame: baseline and 12 weeks
|
Disease Activity Score 28 (DAS28CRP).
Composite index including a non-graded 28 tender and swollen joint count, patients global health (VAS-GH scored 0-100), and CRP in mg/l.
It is based on a complex equasion DAS28 = 0.56 × √[t28] + 0.28 × √[sw28] + 0.70 × Ln [CRP] + 0.014 × GH.
Lower range 0, no higher range.
Higher levels indicating higher disease activity
|
baseline and 12 weeks
|
|
Change in rheumatoid arthritis activity
Time Frame: baseline and 24 weeks
|
Disease Activity Score 28 (DAS28CRP).
Composite index including a non-graded 28 tender and swollen joint count, patients global health (VAS-GH scored 0-100), and CRP in mg/l.
It is based on a complex equasion DAS28 = 0.56 × √[t28] + 0.28 × √[sw28] + 0.70 × Ln [CRP] + 0.014 × GH.
Lower range 0, no higher range.
Higher levels indicating higher disease activity
|
baseline and 24 weeks
|
|
Change in fatigue intensity
Time Frame: baseline and 12 weeks
|
Functional assessment of chronic illness therapy - fatigue (FACIT-F) scale consisting of 13 items.
Range 0-52 with higher scores indicating higher levels of fatigue
|
baseline and 12 weeks
|
|
Change in fatigue intensity
Time Frame: baseline and 24 weeks
|
Functional assessment of chronic illness therapy - fatigue (FACIT-F) scale consisting of 13 items.
Range 0-52 with higher scores indicating higher levels of fatigue
|
baseline and 24 weeks
|
|
Change in anxiety and depression symptoms
Time Frame: baseline and 12 weeks
|
Hospital anxiety and depression scale (HADS) measures levels of anxiety and depression (total score range 0-42 points) consists of subscale for anxiety 0-21 points and sub-scale for depression 0-21 points.
Higher scores indicate higher levels of anxiety / depression.
|
baseline and 12 weeks
|
|
Change in anxiety and depression symptoms
Time Frame: baseline and 24 weeks
|
Hospital anxiety and depression scale (HADS) measures levels of anxiety and depression (total score range 0-42 points) consists of subscale for anxiety 0-21 points and sub-scale for depression 0-21 points.
Higher scores indicate higher levels of anxiety / depression.
|
baseline and 24 weeks
|
|
Change in rheumatoid arthritis impact of disease
Time Frame: baseline and 12 weeks
|
Rheumatoid arthritis impact of disease questionnaire (RAID) is a patient-derived scores assessing 7 most important domains of impact of rheumatoid arthritis.
Domains include pain, functional disability, fatigue, emotional and physical well-being, sleep and coping.
Range 0-10.Higher scores reflect higher levels of symptoms.
|
baseline and 12 weeks
|
|
Change in rheumatoid arthritis impact of disease
Time Frame: baseline and 24 weeks
|
Rheumatoid arthritis impact of disease questionnaire (RAID) is a patient-derived scores assessing 7 most important domains of impact of rheumatoid arthritis.
Domains include pain, functional disability, fatigue, emotional and physical well-being, sleep and coping.
Range 0-10.Higher scores reflect higher levels of symptoms.
|
baseline and 24 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Silva Pukšić, MD, University Hospital Dubrava
- Study Chair: Jadranka Morović-Vergles, MD, PhD, University Hospital Dubrava
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
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
- DUBRAVA-YOGRA-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Rheumatoid Arthritis
-
Centocor, Inc.CompletedRheumatoid Arthritis, Juvenile
-
Janssen Research & Development, LLCWithdrawnActive Rheumatoid Arthritis; Rheumatoid Arthritis
-
Yuanyuan ZhangRecruitingRheumatoid Arthritis (RA) | Rheumatoid Arthritis-Associated Interstitial Lung Disease | Difficult-to-Treat Rheumatoid ArthritisChina
-
AmgenTerminated
-
Children's Hospital Medical Center, CincinnatiNational Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)CompletedJuvenile Rheumatoid ArthritisUnited States
-
AmgenImmunex CorporationCompletedJuvenile Rheumatoid Arthritis
-
Assistance Publique - Hôpitaux de ParisSociete Francaise de RhumatologieRecruiting
-
University Hospital, ToulouseCompletedRheumatoId ArthritisFrance
-
Amsterdam UMC, location VUmcEuropean CommissionCompletedRheumatoId ArthritisNetherlands, Germany, Portugal, Italy, Hungary, Romania, Slovakia
-
David Grant U.S. Air Force Medical CenterCompleted
Clinical Trials on Yoga program
-
Izmir Democracy UniversityEnrolling by invitationPremenstrual Syndrome-PMSTurkey
-
NYU Langone HealthRecruiting
-
Ankara UniversityCompletedRehabilitation | Yoga | Down Syndrome (DS) | Physical Activities | Balance AssessmentTurkey (Türkiye)
-
Istanbul Medipol University HospitalCompletedYoga | Bronchiectasis AdultTurkey (Türkiye)
-
University of OttawaThe Ottawa HospitalCompleted
-
University of Maryland, BaltimoreNational Institute of Nursing Research (NINR)CompletedIrritable Bowel Syndrome | Abdominal PainUnited States
-
University of California, San FranciscoStanford University; National Center for Complementary and Integrative Health...CompletedPelvic Pain | Chronic Pelvic Pain | Recurrent Pelvic PainUnited States
-
Lady Davis InstituteCompletedDementia | Mild Cognitive ImpairmentCanada
-
Hiroshima UniversityCompleted