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Clinical Trials/NCT06176586
NCT06176586
Enrolling By Invitation
Not Applicable

Investigating the Effects of Mat Pilates Exercises in Patients With Axial Psoriatic Arthritis

Izmir Katip Celebi University1 site in 1 country48 target enrollmentJanuary 8, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Psoriatic Arthritis
Sponsor
Izmir Katip Celebi University
Enrollment
48
Locations
1
Primary Endpoint
Change in Physical Performance
Status
Enrolling By Invitation
Last Updated
2 years ago

Overview

Brief Summary

The aim of this study is to investigate the effectiveness of mat Pilates exercises on spinal mobility, spinal muscle endurance, disease activity, fatigue, emotional well-being, physical performance, and overall quality of life in Psoriatic Arthritis (PsA) patients with axial involvement.

Detailed Description

Psoriasis is a chronic inflammatory skin disease commonly accompanied by joint involvement known as psoriatic arthritis (PsA) \[1\]. PsA is a subgroup of spondyloarthritis and is characterized by peripheral arthritis, dactylitis, enthesitis and spondylitis. Axial involvement, which occurs in approximately 40% of PsA patients may affect the entire spine, particularly the sacroiliac joint, leading to reduced cervical rotation, lateral flexion and anterior flexion of the spine \[2,3\]. Exercise interventions in PsA primarily aim to relieve pain, improve mobility and enhance functional capacity \[4\]. Mat Pilates exercises have been demonstrated as a safe and beneficial intervention in various rheumatic diseases, exhibiting significant improvements in functional status, fatigue, disease activity, pain, and overall quality of life \[5-7\]. Additionally, Pilates has been reported as effective in maintaining and enhancing spinal mobility \[8,9\]. However, despite these favorable outcomes, the efficacy of Pilates exercises in PsA remains unexplored. The aim of this study is to investigate the effectiveness of mat pilates exercises in psoriatic arthritis patients with axial involvement.

Registry
clinicaltrials.gov
Start Date
January 8, 2024
End Date
June 10, 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Izmir Katip Celebi University
Responsible Party
Principal Investigator
Principal Investigator

Deniz Bayraktar

Assistant Professor

Izmir Katip Celebi University

Eligibility Criteria

Inclusion Criteria

  • Being classified as PsA according to CASPAR Classification Criteria
  • Being between the ages of 18-65
  • Volunteering to participate in the study

Exclusion Criteria

  • Any additional systemic disease other than PsA
  • Any other condition that may prevent participation/continuation of the exercise program or completion of the assessments
  • Regular exercise habits (following a structured exercise program at least 3 days a week)
  • Being included in a physiotherapy and rehabilitation program within the last 6 months

Outcomes

Primary Outcomes

Change in Physical Performance

Time Frame: At baseline and 12 weeks later

The Ankylosing Spondylitis Performance Index (ASPI) will be used. The ASPI consists of three physical performance tasks: (a) bending forward to pick up six pencils from the floor; (b) putting on socks (average of three repetitions); and (c) getting up from the floor (average of three repetitions). Time to complete a task will be recorded in seconds for each test.

Secondary Outcomes

  • Chance in Disease Activity(At baseline and 12 weeks later)
  • Change in Quality of Life(At baseline and 12 weeks later)
  • Change in Functional Status(At baseline and 12 weeks later)
  • Change in Trunk Muscle Endurance(At baseline and 12 weeks later)
  • Change in Fatigue(At baseline and 12 weeks later)
  • Change in Spinal Mobility(At baseline and 12 weeks later)
  • Change in Emotional Status(At baseline and 12 weeks later)

Study Sites (1)

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