Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
24 participants
INTERVENTIONAL
2016-04-21
2017-12-19
Brief Summary
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Objective: To investigate whether an add-on mindset \& physical therapy program based on the "Wim Hof Method" can safely and efficaciously be applied in patients with active axial spondyloarthritis.
Study design: Prospective open-label randomized controlled trial, safety and efficacy.
Study population: Twenty-four patients with active axial spondyloarthritis between 18 and 45 years of age.
Intervention: A 30-day training program of add-on mindset and physical therapy for axial spondyloarthritis, using the methodology as designed and instructed by Wim Hof. It involves breathing techniques, training of mindset and concentration, and gradual cold exposure.
Main study parameters/endpoints: Safety evaluation of the program is the primary aim of the study. Secondary endpoint is the modulation of serum CRP levels. Exploratory objectives include modulation of clinical disease activity (ASDAS), quality of life (SF-36, EQ-5D), depressive symptoms (HADS), and predictive role of generalized and specific outcome expectancies (EPQ-N, LOT-R, VAS scales).
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Detailed Description
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The techniques of the Wim Hof Method have been modulated to a scientifically reproducible mindset \& physical training program for add-on therapy of axSpA. Specifically, it has been adjusted for potential functional limitations of axSpA.
Primary Objective: To investigate whether the add-on mindset \& physical therapy program can safely be applied in patients with active axSpA using clinical safety parameters.
Secondary Objective: To assess whether the add-on mindset \& physical therapy program can modulate objective signs of inflammation in patients with active axSpA using serum biomarkers (e.g. CRP).
Exploratory objective: To assess whether the add-on mindset \& physical therapy program has an influence on the Ankylosing Spondylitis Disease Activity Score, quality of life, and depressive symptoms (HADS), and to explore the predictive role of generalized and specific outcome expectancies in patients with active axSpA
Conditions
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Study Design
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RANDOMIZED
CROSSOVER
TREATMENT
NONE
Study Groups
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Early intervention group
The program starts with a 30-days training course led by course instructor Wim Hof and supervised by the research team. The mindset \& physical therapy based on the Wim Hof Method includes breathing techniques, training of mindset and concentration, and gradual cold exposure.
Add-on Therapy for Axial Spondyloarthritis
Late intervention group
This group will receive the same training with a delay of 60-90 days, serving initially as control.
Add-on Therapy for Axial Spondyloarthritis
Interventions
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Add-on Therapy for Axial Spondyloarthritis
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Between 18 and 45 years of age at screening
* Active disease as defined by an Ankylosing Spondylitis Disease Activity Score (ASDAS) of \>2.1 and a CRP value of ≥5 at the screening visit.
* Ability and willingness to participate to the study and give written informed consent.
Exclusion Criteria
* Recent history of (or persistent) infection requiring hospitalization or antibiotic treatment within 4 weeks of baseline.
* If female, patient should not be pregnant. A urine pregnancy-test will be performed at screening and has to be negative.
* Initiation of treatment with corticosteroids or DMARDs (synthetic and biologic) within 8 weeks before screening.
* Initiation of treatment with NSAID within 2 weeks before screening.
* Variation of the treatment doses within 6 weeks of screening.
* Intra-articular injection with corticosteroids within 4 weeks prior to screening.
* Daily doses of systemic corticosteroids exceeding the equivalent of 10 mg prednisolone per day.
* Use of other drugs and treatments that may affect the evaluation of systemic inflammation as judged by the investigator.
* Cardiovascular risk factors such as a personal history of cardiovascular disease, familial history of major adverse cardiovascular events (MACE) at age younger than 45 yrs, hypercholesterolemia and stroke.
18 Years
45 Years
ALL
No
Sponsors
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Bernhoven Hospital
OTHER
Radboud University Medical Center
OTHER
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
OTHER
Responsible Party
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D.L.P. Baeten
Professor
Principal Investigators
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Dominique Baeten, MD PhD
Role: PRINCIPAL_INVESTIGATOR
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Locations
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Academic Medical Center
Amsterdam, , Netherlands
Ziekenhuis Bernhoven
Uden, , Netherlands
Countries
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References
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Kox M, Stoffels M, Smeekens SP, van Alfen N, Gomes M, Eijsvogels TM, Hopman MT, van der Hoeven JG, Netea MG, Pickkers P. The influence of concentration/meditation on autonomic nervous system activity and the innate immune response: a case study. Psychosom Med. 2012 Jun;74(5):489-94. doi: 10.1097/PSY.0b013e3182583c6d.
Kox M, van Eijk LT, Zwaag J, van den Wildenberg J, Sweep FC, van der Hoeven JG, Pickkers P. Voluntary activation of the sympathetic nervous system and attenuation of the innate immune response in humans. Proc Natl Acad Sci U S A. 2014 May 20;111(20):7379-84. doi: 10.1073/pnas.1322174111. Epub 2014 May 5.
Buijze GA, De Jong HMY, Kox M, van de Sande MG, Van Schaardenburg D, Van Vugt RM, Popa CD, Pickkers P, Baeten DLP. An add-on training program involving breathing exercises, cold exposure, and meditation attenuates inflammation and disease activity in axial spondyloarthritis - A proof of concept trial. PLoS One. 2019 Dec 2;14(12):e0225749. doi: 10.1371/journal.pone.0225749. eCollection 2019.
Other Identifiers
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Academic_Medical_Center
Identifier Type: -
Identifier Source: org_study_id
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