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Effects of Aerobic Training in Patients With Ankylosing Spondylitis

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01586650
Enrollment
70
Registered
2012-04-27
Start date
2011-07-31
Completion date
2013-02-28
Last updated
2017-02-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ankylosing Spondylitis

Keywords

ankylosing spondylitis, aerobic exercise

Brief summary

This is a randomized controlled trial with blinded assessor on the effects of aerobic exercise (walking)in patients with Ankylosing Spondylitis.

Detailed description

Ankylosing Spondylitis (AS) is a systemic inflammatory disease that affects mainly the spine and compromises globally the physical capacity of the patients. Despite new advances in pharmacological therapy, physiotherapy and exercise remain essential in the treatment of AS. However, the literature lacks studies showing which types of exercises are more effective in patients with AS. This is a randomized controlled trial with the objective is to evaluate the effects of aerobic training on functional capacity, mobility, disease activity, cardiopulmonary capacity and cytokine levels (TNF, IL10, IL6 and IL1) in patients with AS. The duration of the trial is 24 weeks with the first 12 weeks reserved to exercise programs. The participants will be divided in two groups. The intervention group (IG) will perform walking for 50 minutes plus global stretching 3 times a week for 12 weeks. The control group (CG) will do only stretching exercises 3 times a week for 12 weeks.

Interventions

OTHERaerobic training

The intervention comprises fifty minutes of walking at anaerobic threshold plus stretching exercises 3 times a week for 12 weeks.

OTHERStretching exercises

Global stretching exercises will be performed for about 20 minutes 3 times a week for 12 weeks with supervision of specialized physiotherapists.

Sponsors

Fundação de Amparo à Pesquisa do Estado de São Paulo
CollaboratorOTHER_GOV
Federal University of São Paulo
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of Ankylosing Spondylitis according to New York modified criteria. * Stable drug treatment for at least 3 months * Sedentary for at least 3 months before randomization * Steinbrocker class I/II

Exclusion criteria

* Uncontrolled Systemic Arterial Hypertension and Diabetes mellitus. * Ischemic heart disease * Clinically significant diseases * Orthopedic surgery, such as hip arthroplasty, in the last year. * Inability to walk.

Design outcomes

Primary

MeasureTime frameDescription
Change in BASFIBaseline, after 6, 12 and 24 weeks.Bath Ankylosing Spondylitis Functional Index (BASFI) is a quaestionnaire with 10 questions about functional capacity validated to AS patients. Each question is answered with a visual analogue scale 0-10 cm. Zero means the best, and 10 the worst function.

Secondary

MeasureTime frameDescription
Change in BASMIBaseline, after 6, 12 and 24 weeks.Bath Ankylosing Spondylitis Mobility Index (BASMI) is an instrument that comprises 5 measures of mobility validated to AS patients. The measurements are: cervical rotation, lumbar flexion (Schober's test modified, intermalleolar distance, lumbar side flexion and tragus to wall. The total score is shown in a 0-10 cm visual analogue scale. The low scores represent better mobility.
Change in HAQ-SBaseline, after 6, 12 and 24 weeks.Health Assessment Questionnaire for Spondyloarthritis (HAQ-S)is a questionnaire with 10 domains about functional capacity validated to AS patients. The scores ranges from 0 to 3.
Incremental cardiopulmonary exercise testing protocol by treadmillBaseline and after 12 weeks.Incremental cardiopulmonary exercise testing protocol by treadmill is used to measure aerobic capacity of the patients.
Change in BASDAIBaseline, after 6, 12 and 24 weeks.Bath Ankylosing Spondylitis Disease Activity Score (BASDAI) is a instrument with 6 questions about disease activity validated to AS patients. The questions comprise the following areas: back pain, peripheral pain, morning stifness, fatigue and enthesitis.
Levels of cytokines- TNF, IL10, IL6 and IL1.Baseline and after 12 weeks.Cytokines are substances that make part of inflammatory response. The most important cytokines- TNF alpha, IL10, IL6 and IL1 will be measured in serum samples.
Change in the Six minute walking testBaseline, after 6, 12 and 24 weeks.The 6-minute walking test is a instrument to evaluate functional capacity. It is performed measuring the distance that the participant is able to walk during 6 minutes.
Levels of C reactive protein and erythrocyte rate sedimentationBaseline, after 6. 12 and 24 weeksCRP and ESR are laboratory methods to evaluate inflammatory response using blood sample.

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026