Skip to main content
Clinical Trials/NCT02241538
NCT02241538
Completed
Not Applicable

Cost Effectiveness and Effectiveness of the Addition of Different Weekly Frequency of Modified Pilates Method Exercises to a Minimal Intervention in the Treatment of Chronic Nonspecific Low Back Pain: A Randomized Controlled Trial

Universidade Cidade de Sao Paulo1 site in 1 country296 target enrollmentSeptember 2014
ConditionsLow Back Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Low Back Pain
Sponsor
Universidade Cidade de Sao Paulo
Enrollment
296
Locations
1
Primary Endpoint
Pain intensity
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

Low back pain is a major cause of disability and absenteeism and the supervised exercise is a recommended treatment by the guidelines and has been cost-effective. Currently, the Pilates method has shown to be effective in improving pain and disability in patients with chronic low back pain (CLBP). However, there is still no evidence about the ideal number of sessions for the treatment and the interval between sessions to achieve better efficacy of this method for these patients. Thus, the aim of this study is to investigate the effectiveness of the Pilates method with different weekly frequency of sessions in the treatment of patients with nonspecific CLBP. Investigators will assess 296 patients of both genders, with nonspecific CLBP lasting more than three months and aged between 18 and 80 years. Participants will be randomly divided into four groups (n = 74 patients per group): Control Group will receive an educational booklet and no additional exercise, Pilates 1 Group will receive a program of exercises based on Pilates method once a week for six weeks, Pilates 2 Group will receive the same program of exercises twice a week for six weeks and Pilates 3 Group will receive the same program of exercises three times a week for six weeks. The outcomes overall disability (Roland Morris Disability questionnaire), specific disability (Patient-Specific Functional scale), kinesiophobia (Tampa scale for kinesiophobia), pain intensity (Pain Numerical Rating scale) and global perceived effect (Global Perceived Effect scale) will be assessed by a blinded assessor before, six weeks, six and 12 months after randomization. Investigators expect that the largest number of weekly sessions of Pilates method may influence the results in all analyzes (short, medium and long term), since there is a relationship between frequency of exercises and effect size of the treatment.

Registry
clinicaltrials.gov
Start Date
September 2014
End Date
June 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Universidade Cidade de Sao Paulo
Responsible Party
Principal Investigator
Principal Investigator

Cristina Maria Nunes Cabral

Associate Professor

Universidade Cidade de Sao Paulo

Eligibility Criteria

Inclusion Criteria

  • Patients with chronic nonspecific low back pain longer 12 weeks

Exclusion Criteria

  • Contra indications to physical exercise
  • Serious spinal pathologies (e. g. tumors, fractures and inflammatory diseases)
  • Nerve root compromise
  • Pregnancy
  • Previous surgery on spine
  • Pilates treatment for low back pain in the last three months

Outcomes

Primary Outcomes

Pain intensity

Time Frame: Six weeks after randomization

Pain intensity will be measured by an 11-point Pain Numerical Rating Scale

Disability

Time Frame: Six weeks after randomization

Disability associated with low back pain will be measured by the 24-item Roland Morris Disability Questionaire

Secondary Outcomes

  • Disability(Six and twelve months after randomization)
  • Global impression of recovery(Six weeks, six and twelve months after randomization)
  • Cost Effectiveness(Six weeks, six and twelve months after randomization)
  • Quality Adjusted Life Years(Six weeks, six and twelve months after randomization)
  • Pain intensity(Six and twelve months after randomization)
  • Specific disability(Six weeks, six and twelve months after randomizaion)
  • Kinesiophobia(Six weeks, six and twelve months after randomization)
  • Pain-Related Catastrophizing(Six weeks, six and twelve months after randomization)

Study Sites (1)

Loading locations...

Similar Trials