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Resistance Training Exercise Using the Swiss Ball in Ankylosing Spondylitis

Assessment of Effectiveness of Resistance Training Exercise Using the Swiss Ball in Patients With Ankylosing Spondylitis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01351311
Enrollment
60
Registered
2011-05-10
Start date
2011-03-31
Completion date
2012-11-30
Last updated
2012-11-30

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

Conditions

Ankylosing Spondylitis

Keywords

treatment, exercise, resistance training, swiss ball, functional capacity

Brief summary

The aim of the present study is to assess the effectiveness of resistance training with swiss ball in the treatment of patients with ankylosing spondylitis.

Detailed description

A randomized, controlled, single-blind, prospective trial being conducted involving 54 patients with ankylosing spondylitis, selected from outpatient clinics - UNIFESP. They will be randomized in intervention group (n = 27) conduct training for muscle strengthening with the aid of the Swiss ball and in the control group (n = 27) did not undergo any intervention. Eight exercises will be conducted with intent to engage all muscle groups.

Interventions

OTHERExercise

Resistance Training exercise with swiss ball

Drug treatment

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

* Patients with established diagnosis of AS steinbrocker functional class I-II * Basic medication stable for at least three months * Agreed to participate and signed term of informed consent

Exclusion criteria

* Uncontrolled hypertension * Coronary artery disease * History of revascularization * History of syncope or arrhythmias induced by exercise * Decompensated diabetes mellitus * Severe psychiatric illness * Fibromyalgia * Another medical condition more disabling than AS * History of exercise regular (at least 30 minutes 2 times per week)

Design outcomes

Primary

MeasureTime frameDescription
Bath Ankylosing Spondylitis Functional Index (BASFI)16 weeksFunctional capacity assessed by BASFI

Secondary

MeasureTime frameDescription
1 REPETITION MAXIMUM TEST16 weeksmuscle strength by testing an repetition maximum (1 RM)
Bath Ankylosing Spondylitis Disease Activity Index (BASDAI)16 weeksdisease activity by BASDAI (The Bath Ankylosing Spondylitis Disease Activity Index)
Bath Ankylosing Spondylitis Metrology Index (BASMI)16 weeksspinal mobility by BASMI
erythrocyte sedimentation rate (ESR)16 weeks
LIKERT SCALE16 weeksLikert scale by patients.
TIME UP AND GO TEST16 weeks
Short form-36 (SF-36)16 weeksquality of life by SF-36
QUANTITY OF ANALGESICS AND ANTI-INFLAMATORY USED16 weeks
Health Assessment Questionnaire (HAQ) Health Assessment Questionnaire16 weeksFunction
6-MINUTE WALK TEST16 weeks

Countries

Brazil

Outcome results

None listed

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