Skip to main content
Clinical Trials/NCT02598739
NCT02598739
Completed
Not Applicable

Resistance Training in Patients With Psoriatic Arthritis Improves Function, Disease Activity and Quality of Life

Federal University of São Paulo1 site in 1 country41 target enrollmentMay 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Psoriatic Arthritis
Sponsor
Federal University of São Paulo
Enrollment
41
Locations
1
Primary Endpoint
Change in the functional capacity
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The aim of this study was to assess the effectiveness of resistance training in improving functional capacity, muscle strength, quality of life and disease activity in patients with PSA.

Detailed Description

The IG patients performed resistance exercises for the following muscles group: upper limbs, lower limbs and trunk. It was used a machine "leg extension" for the training on the lower limbs. For upper limbs we used a pulley triceps machine and front pull in addition to free weights (dumbbells). In order to perform the exercise program the study followed all the recommendations established by the American College of Sports Medicine (ACSM) (Ratamess et al., 2009). It was carried out two exercises for major muscle groups and one exercise for small muscles. The exercises were divided in 3 sets of 12 repetitions for each muscle group. The intensity of the exercises were 60% of one-maximum repetition (1RM). The exercise program involved pectoral exercises: crucifix and seat supine; biceps: alternated screw; triceps: triceps pulley; back: standing handsaw and pulled ahead; quadriceps: leg extensor and finally gluteo: standing hips extension. Control Group (CG) The control group was kept in a waiting list while continued with the standard pharmacological treatment during all the study. The patients were instructed to maintain their daily activities and to avoid any other non-pharmacological treatment. The exercise program was offered to the control group in the end of the study.

Registry
clinicaltrials.gov
Start Date
May 2014
End Date
December 2014
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Federal University of São Paulo
Responsible Party
Principal Investigator
Principal Investigator

Diego Roger Silva

Principal Investigator

Federal University of São Paulo

Eligibility Criteria

Inclusion Criteria

  • Confirmed diagnosis of psoriatic arthritis, according to the CASPAR criteria
  • Between 18 and 65 years of age, of both genders who agreed and signed the consent form.
  • Patients should be-modifying drugs (DMARDs) on stable doses for at least three months and doses of non-steroidal anti-inflammatory drugs and corticosteroids stable for at least 4 weeks

Exclusion Criteria

  • Patients were excluded:
  • Uncontrolled cardiovascular disease
  • Decompensated diabetes mellitus; diseases
  • Severe psychiatric
  • Fibromyalgia
  • Other medical conditions that most disabling EA
  • History of regular exercise (at least 30 minutes 2 times per week) during the last 6 months
  • Arthroplasties of the hip and / or knee in the last 12 months; AND
  • Any other medical condition that prevents the patient from performing resistance exercises

Outcomes

Primary Outcomes

Change in the functional capacity

Time Frame: Baseline, after 45 and 90 days

Evaluated by HAQ-S Health Assessment Questionnaire for the Spondylarthropathies

Secondary Outcomes

  • Change in the quality of life(Baseline, after 45 and 90 days)

Study Sites (1)

Loading locations...

Similar Trials