- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06083090
Effects of Yoga Therapy in Rehabilitation Compared to Physiotherapy in Moderate Axial Spondyloarthritis (axSPA) (YOKISPA)
Effects of Yoga Therapy in Rehabilitation Compared to Physiotherapy in Moderate Axial Spondyloarthritis (axSPA): a Randomized Controlled Multicenter Study.
A few studies have evaluated the effectiveness of yoga therapy in patients with axial spondyloarthritis (axSPA). On the other hand, studies conducted in other chronic rheumatisms such as low back pain, rheumatoid arthritis or other conditions such as cancer have shown that yogatherapy can have a effective action on the physical and psychological level.
Yogatherapy is a non-drug "body-mind" approach that would be likely to improve the physical symptoms (pain, stiffness, in particular spinal and pelvic), internal organs (colitis) and psychological symptoms as well as the perception of fatigue of people with axSPA. A 2021 study showed the feasibility and acceptability of regular yogatherapy practice in patients with axSPA.
It is therefore necessary to conduct randomized controlled studies to assess the effectiveness of this management strategy.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The term axial spondyloarthritis (axSPA) encompasses various inflammatory diseases of the spine, including ankylosing spondyloarthritis (AS) and non-radiographic axial spondyloarthritis (nr-axSPA).
axSPA is a chronic inflammatory joint disease affecting the axial skeleton. It is the second cause of chronic inflammatory rheumatism and affects 0.5 to 2% of the general population. It generally affects young adults, with a male predominance (2 men for 1 woman).
axSPA can lead to physical consequences (fatigue, pain, stiffness, with in particular serious damage to the spine causing functional impairment, etc.) and psychological consequences (anxiety, depression). It is responsible for a disability and a mediocre quality of life with, moreover, a significant socio-economic impact. In France, it is one of the long-term illnesses and may require heavy treatment.
The medicinal therapeutic side, taken care of by rheumatologists specializing in this pathology, has evolved a lot (from non-steroidal anti-inflammatory drugs [NSAIDs] to anti-tumor necrosis factor [anti-TNF] and anti-interleukin 17 [anti-IL 17]), allowing notable improvements. It is now a question of also developing the non-drug therapeutic side, to contribute to improving the quality of life, thus meeting the demand of patients with chronic diseases.
Information and therapeutic education occupy an important place, with results in favor of an improvement in the management of these diseases.
The recommendations emphasize that the non-pharmacological treatment of axSPA should include regular physical exercise, that individual and group physical therapy sessions should be considered as well as self-exercises.
Several randomized controlled trials have shown that physical therapy with various modalities has positive effects on pain and AS function. Physical therapy therefore also seems to play an important role in the management of patients. It prevents stiffness and improves functional capacity and quality of life.
Physical therapy should be initiated as soon as axSPA is diagnosed and regular exercise should form the basis of management. The review by Zochling et al. as well as a systematic review showed that exercises have positive effects on BASFI, BASDAI functions, pain and mobility. A Cochrane review on the role of physiotherapy interventions in SPA also concluded that physical therapy was beneficial. Physical activity, self-exercises and physiotherapy are part of the 2022 recommendations of the French Society of Rheumatology. Beneficial effects on disease activity were observed in axSPA, with good tolerance for intense exercise.
Recently an Indian team evaluated the effectiveness of online yogatherapy with 60 min structured modules on patients with axSPA for 3 months, with a significant improvement in the BASDAI score.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Charlotte PAUWELS
- Phone Number: +33 1 49 81 30 66
- Email: charlotte.pauwels@aphp.fr
Study Contact Backup
- Name: Petra PAREJO MARGALLO
- Phone Number: +33 1 40 27 43 13
- Email: petri.parejo-margallo@aphp.fr
Study Locations
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Bobigny, France, 93000
- Recruiting
- Hôpital Avicenne
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Contact:
- Nathalie SAIDENBERG-KERMANAC'H
- Phone Number: +33 +1 48 95 54 44
- Email: nathalie.saidenberg@aphp.fr
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Créteil, France, 94010
- Recruiting
- Hôpital Henri Mondor
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Contact:
- Laura PINA-VEGAS
- Phone Number: +33 1 49 81 47 04
- Email: laura.pinavegas@aphp.fr
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Créteil, France, 94000
- Active, not recruiting
- Hôpital Henri Mondor
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Paris, France, 75014
- Recruiting
- Hôpital Cochin
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Contact:
- Olivier FOGEL
- Phone Number: +33 1 58 41 25 63
- Email: olivier.fogel@aphp.fr
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Paris, France, 75013
- Active, not recruiting
- Hopital Pitie Salpetriere
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- French-speaking patient aged 18 and over
- Patient with axial spondyloarthritis (axSPA) according to Assessment of SpondyloArthritis International Society, diagnosed by a rheumatologist
- "Moderately active" to "active" form of axSPA (basic BASDAI > 3)
- Stable disease: No recent or foreseeable introduction in the next 6 months of drug treatments for axSPA (excluding analgesics)
- Absence of disabling stress urinary incontinence
- Geographical or organizational possibility of undergoing the study
- Patient informed and having signed the informed consent form for participation in the research
Exclusion Criteria:
- Pregnancy or breastfeeding
- Recent childbirth (within the last six months)
- Patient already practicing yoga or having practiced it in the last six months
- Abdominal or spinal surgery in the last six months
- Motor neurological deficit
- Sphincter deficit
- Any other somatic pathology preventing the practice of physiotherapy or yogatherapy according to the opinion of the evaluating clinician
- Depressive syndrome requiring specific treatment
- Non-affiliation to a social security scheme (beneficiary or beneficiary) or to another social protection scheme
- Patient deprived of liberty by judicial or administrative decision or under legal protection (guardianship, safeguard of justice)
- Currently participating in or in a period of exclusion from: another interventional research involving human participants, a clinical trial on a medical product for human, a clinical investigation on a medical device. Participation in non-interventional research is authorized.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Yogatherapy
Randomization of 36 patients in the yogatherapy group.
|
The experimental arm will benefit from support by a physiotherapist trained in yoga, in a group for ten weeks with two weekly sessions of approximately 1 hour each.
A new yoga program adapted for the axSPA will be implemented.
|
|
Active Comparator: Physiotherapy
Randomization of 36 patients in the physiotherapy group.
|
The comparator arm will benefit from support by a physiotherapist, in groups for ten weeks at the rate of two weekly sessions of approximately 1 hour each.
An already existing program adapted for the axSPA will be implemented.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Evolution of the axSPA global activity score (fatigue, pain, stiffness)
Time Frame: Between the 2 month visit and the 5 month visit.
|
Change in the BASDAI (Bath Ankylosing Spondylitis Disease Activity Index) score, via a self-administered questionnaire that assesses the "activity" of the disease (6 items, max score = 100, the higher the score the more disabling the disease).
|
Between the 2 month visit and the 5 month visit.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Evolution of the axSPA global activity score (fatigue, pain, stiffness)
Time Frame: Between the 2 month visit and the 5 month visit. Between the 2 month visit and the 11 month visit.
|
Change in the BASDAI (Bath Ankylosing Spondylitis Disease Activity Index) score, via a self-administered questionnaire that assesses the "activity" of the disease (6 items, max score = 100, the higher the score the more disabling the disease).
|
Between the 2 month visit and the 5 month visit. Between the 2 month visit and the 11 month visit.
|
|
Functional impact
Time Frame: Between the 2 month visit and the 5 month visit. Between the 2 month visit and the 11 month visit.
|
Change in self-assessment of functional capacity during daily tasks via the BASFI score (Bath Ankylosing Spondylitis disease Functional Index) (10 items, max score = 10, the higher the score the more disabling the disease).
|
Between the 2 month visit and the 5 month visit. Between the 2 month visit and the 11 month visit.
|
|
Anxiety and depression
Time Frame: Between the 2 month visit and the 5 month visit. Between the 2 month visit and the 11 month visit.
|
Change in the patient's self-assessment via the HAD scale (Hospital Anxiety and Depression scale) (14 items, max anxiety score = 21, max depression score = 21, the higher the score the more anxiety and depressive disorders are marked).
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Between the 2 month visit and the 5 month visit. Between the 2 month visit and the 11 month visit.
|
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Respiratory capacity
Time Frame: Between the 2 month visit and the 5 month visit. Between the 2 month visit and the 11 month visit.
|
Measurement of chest expansion.
|
Between the 2 month visit and the 5 month visit. Between the 2 month visit and the 11 month visit.
|
|
Spinal and axial mobility (maximum active amplitudes - sagittal plane)
Time Frame: Between the 2 month visit and the 5 month visit. Between the 2 month visit and the 11 month visit.
|
Change in measurement of maximum active amplitudes in orthostatism of the thoraco-lumbar spine in the sagittal (flexion/extension) plane.
|
Between the 2 month visit and the 5 month visit. Between the 2 month visit and the 11 month visit.
|
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Spinal and axial mobility (degrees of kyphosis and lordosis)
Time Frame: Between the 2 month visit and the 5 month visit. Between the 2 month visit and the 11 month visit.
|
Change in measurement of the degrees of kyphosis and lordosis while standing.
|
Between the 2 month visit and the 5 month visit. Between the 2 month visit and the 11 month visit.
|
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Spinal and axial mobility (maximum active amplitudes - frontal plane)
Time Frame: Between the 2 month visit and the 5 month visit. Between the 2 month visit and the 11 month visit.
|
Change in measurement of maximum active amplitudes in orthostatism of the thoraco-lumbar spine in the frontal (lateral inclinations) plane.
|
Between the 2 month visit and the 5 month visit. Between the 2 month visit and the 11 month visit.
|
|
Spinal and axial mobility (podobarometric treadmill)
Time Frame: Between the 2 month visit and the 5 month visit. Between the 2 month visit and the 11 month visit.
|
Change in measurement of the spatiotemporal analysis of gait on a podobarometric treadmill.
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Between the 2 month visit and the 5 month visit. Between the 2 month visit and the 11 month visit.
|
|
Axial mobility
Time Frame: Between the 2 month visit and the 5 month visit. Between the 2 month visit and the 11 month visit.
|
Change in BASMI (Bath Ankylosing Spondylitis Metrology Index) score (5 items, max score = 10, the higher the score the more restricted the axial mobility).
|
Between the 2 month visit and the 5 month visit. Between the 2 month visit and the 11 month visit.
|
|
Follow-up of the therapeutic strategy
Time Frame: Between the 2 month visit and the 5 month visit. Between the 2 month visit and the 11 month visit.
|
Change in therapeutic strategy.
|
Between the 2 month visit and the 5 month visit. Between the 2 month visit and the 11 month visit.
|
|
Drug consumption monitoring
Time Frame: Between the 2 month visit and the 5 month visit. Between the 2 month visit and the 11 month visit.
|
Change in drug consumption.
|
Between the 2 month visit and the 5 month visit. Between the 2 month visit and the 11 month visit.
|
|
Sleep quality
Time Frame: Between the 2 month visit and the 5 month visit. Between the 2 month visit and the 11 month visit.
|
Change in QESL score (Leeds Sleep Assessment Questionnaire) (10 visual analog scales, minimum = -50, maximum = 50, the higher the score the better the sleep).
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Between the 2 month visit and the 5 month visit. Between the 2 month visit and the 11 month visit.
|
|
Adherence to the practice of yogatherapy of patients randomized in this group
Time Frame: After physical rehabilitation : at 5 month and 11 month visits.
|
Degree of adherence to the practice of yogatherapy collected through responses to a short self-questionnaire.
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After physical rehabilitation : at 5 month and 11 month visits.
|
|
Health-related quality of life
Time Frame: Between the 2 month visit and the 5 month visit. Between the 2 month visit and the 11 month visit.
|
Change in the patient's self-assessment via the generic SF-36 scale (Short Form-36 scale) (36 items, max score = 100, the higher the score the better the perception of quality of life).
|
Between the 2 month visit and the 5 month visit. Between the 2 month visit and the 11 month visit.
|
Collaborators and Investigators
Investigators
- Study Director: Petra PAREJO MARGALLO, Assistance Publique - Hôpitaux de Paris
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Bone Diseases
- Musculoskeletal Diseases
- Arthritis
- Joint Diseases
- Connective Tissue Diseases
- Spinal Diseases
- Spondylarthropathies
- Ankylosis
- Spondylarthritis
- Spondylitis
- Skin and Connective Tissue Diseases
- Axial Spondyloarthritis
- Spondylitis, Ankylosing
- Rheumatic Diseases
- Therapeutics
- Rehabilitation
- Physical Therapy Modalities
Other Study ID Numbers
- APHP210998
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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 Axial Spondyloarthritis (axSPA)
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University of BonnNovartis; Novartis PharmaceuticalsRecruitingAxial Spondyloarthritis | Axial and Peripheral Spondyloarthritis | Axial Spondyloarthopathy | Axial Spondyloarthritis and Ankylosing Spondylitis | Axial Spondyloarthritis (AxSpA) | Axial Spondylarthritis (r-axSpA) | Axial Spondyloarthritis, Non-RadiographicGermany
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Grey Wolf TherapeuticsRecruitingAxial Spondyloarthritis (AxSpA)Belgium, Poland, Netherlands, Australia, Germany, Spain
-
Ángel Alberich BayarriCompletedAxial Spondyloarthritis (AxSpA)United Arab Emirates, Saudi Arabia, Jordan, Spain
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UCB BIOSCIENCES GmbHCompletedAxial Spondyloarthritis | Nonradiographic Axial Spondyloarthritis | Nr-axSpAUnited States, Australia, Bulgaria, Canada, Czechia, Hungary, Poland, Russian Federation, Taiwan
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Assistance Publique Hopitaux De MarseilleCompletedAnkylosing Spondylitis (AS) | Axial Spondyloarthritis (axSpA)France
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Yeşim Ozge Gunduz GulAnkara Diskapi Training and Research HospitalCompletedAerobic Exercise | Disease Activity | Axial Spondyloarthritis (AxSpA)Turkey
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The Affiliated Nanjing Drum Tower Hospital of Nanjing...CompletedSecukinumab | Axial Spondylarthritis (axSpA)China
Clinical Trials on Yogatherapy
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