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Type 1 Interferon Induced Changes to Exercise Adaptations in Systemic Lupus
Investigating the physiological effects of the interferons type 1 and 2 (IFNs), and the cytokines Interleukin 6 (IL-6) and tumor necrosis factor (TNF) on the adaptive changes to exercise in patients with systemic lupus erythematosus (SLE). The investigators hypothesize that the pathogenic blockage of IL-6 signalling that occurs in SLE, will decrease the cardiac and metabolic adaptations to aerobic exercise, and this decrease can be related to the IFN signature. 55 patients was included in a 12-week investigator blinded 1:1 randomised high intensity aerobic exercise intervention study.
55 patients with SLE have been included and randomized in a 1:1 fashion to a 12 week high intensity interval training (HIIT) course or standard care. Randomization was stratified by sex. All patients will undergo baseline and followup testing including: VO2Max, Pulmonary Function, Capillaroscopy, OGTT, Blood Tests, Epigenetic Markers of IFN, TNF and IL-6 signalling, Echocardiography,DXA, Medical Examination, Acute Exercise Bout with blood tests during and after an exercise bout similar to the intervention. A subgroup of patients will be offered a 82-Rb Pet CT of the heart as opt-in. The exercise programme consists of 12 weeks of tri-weekly exercise bouts of 38-45 minutes, following warm-up subjects will undergo 4 sets of 4 minute high intensity exercise, measured as the pulse being above 85% of HRmax for more than half the time; and 3 minute low to medium intensity exercise between the high intensity sets, measured as the pulse being between 40 to 60% of HRmax.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Center for Physical Activity Research
Copenhagen, Denmark
Start Date
April 1, 2022
Primary Completion Date
April 16, 2024
Completion Date
January 1, 2025
Last Updated
September 9, 2025
55
ACTUAL participants
High Intensity Interval Training (HIIT)
BEHAVIORAL
Lead Sponsor
Rigshospitalet, Denmark
Collaborators
NCT06647069
NCT07371468
Data Source & Attribution
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View ClinicalTrials.gov Terms and ConditionsNCT06333483