A simpler fitness test could empower spondylarthritis patients to monitor their heart health
NCT ID NCT05926453
First seen Aug 19, 2026 · Last updated Aug 20, 2026 · Updated 1 time
Summary
This study is testing whether a simpler, less expensive treadmill test can accurately measure cardiorespiratory fitness in people with spondylarthritis, a chronic inflammatory joint disease. The simpler test will be compared against the gold standard, which uses direct gas exchange measurements. If validated, this easier test could be used more widely in hospitals and community settings, helping patients track their fitness and reduce their risk of cardiovascular disease.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Maximal cardiorespiratory exercise test using the modified Balke protocol on a treadmill
- What this could lead to
- If the simpler test proves accurate, it could make fitness testing more accessible for people with spondylarthritis, helping them manage their condition and reduce cardiovascular risk.
- What could go wrong
- The trial is small and early, and the simpler test may not match the accuracy of the gold standard in this specific patient group.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
55 people
The number who actually took part.
- Started
-
Oct 2023
- Expected to finish
-
Jun 2029
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients with spondylarthritis diagnosed by a rheumatologist
- Ages
-
18 to 70 years
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adult patients 18-70 years old with axial SpA according to ASAS criteria Exclusion Criteria: * The American College of Sports Medicine (ACSM) have listed the following contradictions to CPET and participants with absolute or relative contradictions will be excluded. * Absolute contraindications to max CPET: acute myocardial infarction within 2 days, unstable angina, uncontrolled cardiac arrhythmia with hemodynamic compromise, active endocarditis, symptomatic severe aortic stenosis, decompensated heart failure, acute pulmonary embolism, pulmonary infarction, or deep venous thrombosis, acute myocarditis or pericarditis, suspected or known aneurysm, acute systemic infection accompanied by fever, body aches, or swollen lymph glands. * Relative contraindications to max CPET: Left main coronary stenosis, moderate to severe aortic stenosis, arrhythmia (tachydysrhythmia or bradyarrhythmia), recent stroke or transient ischemic attack, resting hypertension with blood pressure systolic \> 200 mmHg and/or diastolic \> 115 mmHg, uncorrected medical conditions, such as significant anaemia, important electrolyte abnormalities imbalance, and hyperthyroidism, uncontrolled metabolic disease (e.g. diabetes, thyrotoxicosis or myxoedema) and chronic infectious disease (e.g. mononucleosis, hepatitis, AIDS). * For the SpA population we have included the following specific exclusion criteria: Unable to walk for less than 15 minutes without support, pregnancy, active uveitis, under- or overweight (BMI: ≤ 18.5 or \> 40)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Diakonhjemmet hospital
Oslo, Norway
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