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Effectiveness of Mat Pilates Exercises in Individuals With Chronic Nonspecific Low Back Pain

Effectiveness of Mat Pilates Exercises in Individuals With Chronic Nonspecific Low Back Pain: A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02922322
Enrollment
30
Registered
2016-10-04
Start date
2016-02-29
Completion date
2016-05-31
Last updated
2016-10-04

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

Conditions

Nonspecific Chronic Low Back Pain, Chronic Low Back Pain

Keywords

Mat Pilates, Chronic Nonspecific low back pain, Quality of life, Disability, transverse abdominal muscle

Brief summary

To analyze the effectiveness of mat Pilates compared to no intervention in individuals with chronic nonspecific low back pain.

Detailed description

There is evidence that exercises based on the Pilates method reduce pain in chronic nonspecific low back pain (CNLBP). However, is noticed the lack of studies that compare the effectiveness of mat Pilates to no intervention in the treatment of individual with CNLBP. Therefore, the main objective of the study is to analyze the effectiveness of mat Pilates compared to no intervention in patients with chronic nonspecific low back pain. It is a randomized controlled trial with two arms and double blinded (caregiver, assessor and outcome assessor), composed of 30 patients, aged between 18- 65 years (±22,47) of both sexes, diagnosed with chronic non-specific low back pain persisting for more than three months and pain intensity greater than 3 points in the Pain Numerical Rating Scale. The participants were randomly divided into two groups: Pilates Group (n = 15), intervention based on mat Pilates exercises, and Control Group (n =15) with no intervention. The mat Pilates group performed 16 sessions, twice a week in 60-minute duration each throughout eight weeks, whereas the control group participants kept usual cares until the end of the intervention. Both groups were evaluated before and after the program by a researcher who was unaware of the patients' allocation. The primary assessed outcomes: pain intensity (Pain numerical rating scale, and McGill questionnaire), quality of life (SF-36), and disability (Oswestry Low Back Pain Disability Questionnaire). In addition, the strength and muscle activation of transverse abdominal as secondary outcome assessed through the Stabilizer Pressure Biofeedback Unit test. As a result, the study infers that mat Pilates exercises have significantly improved all the evaluated outcomes. Thus, supporting clinical decisions for the treatment of chronic nonspecific low back pain.

Interventions

The Pilates group program (PG) was composed of 16 sessions, 2x per week, 60 minute session each for 8 weeks. The intervention was based on 20 out of the 34 original mat exercises proposed by the Pilates method, classified into basic, intermediate or advanced levels divided into 4 cycles of 5 exercises each. The exercises were performed during two series of 10 repetitions respecting the patients skills.

Sponsors

Federal University of Paraíba
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Caregiver, Investigator, Outcomes Assessor)

Eligibility

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

Inclusion criteria

* Complaining of non-specific low back pain for more than three months without radicular symptoms for a period exceeding 12 months. * Pain intensity equal to or more than 3 points evaluated by the Pain Numerical Rating Scale in the last seven days. * Eligibility to practice physical activity responding to the Physical Activity Readiness Questionnaire - PAR-Q

Exclusion criteria

* Degenerative or inflammatory pathologies of the spine, * Acute crisis of pain in the shoulders, knees, ankles and spine * Spinal tumors * Recent surgery on the spine, lower and upper limbs * Herniated disc * Spondylolysis or spondylolisthesis * Rheumatologic diseases * Patients who are in labor dispute * In treatment involving Pilates, physiotherapy or medication. * Do not understand the writing and speaking Portuguese.

Design outcomes

Primary

MeasureTime frameDescription
Questionnaire on Pain Intensity8 weeksThe pain intensity was evaluated using an 11-point pain numerical rating scale.

Secondary

MeasureTime frameDescription
Questionnaire on Quality of Life8 weeksThe quality of life assessment was measured through the SF-36 questionnaire.
Questionnaire on Disability8 weeksThe index of disability was assessed trough the 2.0 version of the Oswestry questionnaire, which is a specific questionnaire to evaluate levels of disability in people who suffer with low back pain.
Questionnaire on Pain Describers8 weeksThe pain describers were evaluated through the MCGill questionnaire.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026