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Interval Training Study in Psoriatic Arthritis

Interval Training Study in Psoriatic Arthritis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02995460
Enrollment
67
Registered
2016-12-16
Start date
2013-01-31
Completion date
2015-12-31
Last updated
2018-11-13

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

Conditions

Psoriatic Arthritis

Keywords

Exercise Therapy

Brief summary

Psoriatic arthritis is a chronical inflammatory disease characterized by pain and reduced physical function. Patients have a higher risk of cardiovascular disease and a higher body mass index. A pilot study in patients with rheumatoid arthritis has shown positive effect on inflammation after 12 weeks of high-intensity interval training. The primary aim of this study is to determine whether high-intensity interval training affects the disease activity in psoriatic arthritis. This intervention is believed to result in benefits in terms of inflammation, body composition and risk factors for cardiovascular disease.

Interventions

BEHAVIORALinterval training

4x4 high intensity interval training

Sponsors

Helse Midt-Norge
CollaboratorOTHER
Norwegian University of Science and Technology
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* fulfilling the CASPAR criteria of psoriatic arthritis * ability to exercise.

Exclusion criteria

* Inability to exercise * very high disease Activity * unstable ischemic cardiovascular disease * severe pulmonary disease * pregnancy * breastfeeding * drug- and alcohol addictions

Design outcomes

Primary

MeasureTime frameDescription
Maximal oxygen uptake (VO2 max)Baseline, 3 months (right after intervention), 9 monthsThe VO2 max is measured as a change between timepoints
Patient global assesment (PGA)Baseline, 3 months (right after intervention), 9 monthsPGA is measured as a change between timepoints. PGA is registered by the patient on a visual analog scale.

Secondary

MeasureTime frameDescription
Total lean massBaseline, 3 months (right after intervention), 9 monthsTotal lean mass is measured as a change between timepoints and is measured by dual energy x-ray absorptiometry (DXA).
Total body fatBaseline, 3 months (right after intervention), 9 monthsTotal body fat is measured as a change between timepoints and is measured by dual energy x-ray absorptiometry (DXA).

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 8, 2026