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Clinical Trials/NCT02995460
NCT02995460CompletedNot Applicable

Interval Training Study in Psoriatic Arthritis

Norwegian University of Science and Technology0 sites67 target enrollmentStarted: January 2013Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
67
Primary Endpoint
Patient global assesment (PGA)

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts 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

Outcomes

Primary Outcomes

Patient global assesment (PGA)

Time Frame: Baseline, 3 months (right after intervention), 9 months

PGA is measured as a change between timepoints. PGA is registered by the patient on a visual analog scale.

Maximal oxygen uptake (VO2 max)

Time Frame: Baseline, 3 months (right after intervention), 9 months

The VO2 max is measured as a change between timepoints

Secondary Outcomes

  • Total lean mass(Baseline, 3 months (right after intervention), 9 months)
  • Total body fat(Baseline, 3 months (right after intervention), 9 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

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