- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03113292
Effects of the Pilates Method Versus Home Exercise in Individuals With Chronic Non-specific Back Pain (COmEBACK)
Effectiveness and Cost-effectiveness of the Pilates Method Versus Home-based Exercises in Individuals With Chronic Non-specific Low Back Pain: a Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Brasília, Brazil
- Campus UnB Ceilandia
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Presence of chronic non-specific back pain for more than 12 consecutive weeks;
- Not having attended Pilates or physiotherapy sessions for at least 6 months prior to enrollment.
Exclusion Criteria:
- History of trauma or fractures in the spine;;
- Diagnosis of osteoarthritis, disc herniation or spondylolisthesis;
- Referred pain (visceral, abdominoplasty, appendicitis, abdominal and pelvic surgeries);
- Previous surgery on the spine;
- Presence of root symptoms;
- Pregnancy.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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EXPERIMENTAL: Pilates Method
Mat Pilates Program, 2x/week, for 6 weeks, supervised by a Physiotherapist.
Sessions will last forty five min, with 4 individuals per session.
On average, 10 to 15 exercises will be performed per session, with repetitions ranging from 10 to 20 times, according subject's limitations.
If necessary, the exercises will be adapted individually for the three levels of difficulty: basic, intermediate and advanced.
Progress will be dependent on the absence of postural compensations when performing the repetitions of the exercises.
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The protocol will be composed by the following exercises, structured in each session according to progression, difficulty and focus (respiration, stability, muscle strength and joint mobility): Arm Arcs, Bent Knee Opening, Sidelying, Dead Bug, Femur Arcs, Quadruped Series, Single Leg Stretch, Prone Press Up, Sidekick (Front to Back 1 e 2), Leg Pull Front, Mermaid, Spine Stretch, The Hundred, Pelvic Clock, Bridging, Stanging Roll Down, Swan, Saw, Dart, Swimming, Book Opening. .
Other Names:
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ACTIVE_COMPARATOR: Home Exercise Prescription
Composed by two familiarization sessions, supervised by a Physiotherapist.
The protocol include postural reeducation exercises, stretching and muscle strengthening, stabilization and mobilization of the spine.
Subsequently, participants will receive an educational booklet containing information on low back pain, anatomy of the spine and its relation to the muscular chain, care during daily life activities and the importance of regular physical exercises.
Also, it will include a booklet with the prescription of therapeutic home exercises to be performed during the next 6 weeks.
It will be recommended that the participants perform the exercises 2x/week.
Participants will also be contacted weekly by email and/or telephone, for remote supervision and for checking the prescribed exercises.
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The protocol will be divided into 3 phases, each one composed by the following exercises and structured according to difficulty progression and focus (postural reeducation, muscle strength, balance, joint flexibility): Muscle strength exercises composed by abdominal exercises; back extension exercises; gluteus maximus exercises.
Stretching exercises for the lower back, pelvis, iliopsoas muscle, tensor fascia latae muscle).
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Pain Intensiy
Time Frame: Change from Pre-Intervention (baseline) compared to Post-Intervention (6 weeks) and Follow-up (6 months)
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Pain Intensity measured on a Visual Analog Scale (VAS, in centimeters)
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Change from Pre-Intervention (baseline) compared to Post-Intervention (6 weeks) and Follow-up (6 months)
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Disability
Time Frame: Change from Pre-Intervention (baseline) compared to Post-Intervention (6 weeks) and Follow-up (6 months)
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Quebec Back Pain Disability Scale, scores ranging from 0 to 100
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Change from Pre-Intervention (baseline) compared to Post-Intervention (6 weeks) and Follow-up (6 months)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Health status
Time Frame: Change from Pre-Intervention (baseline) compared to Post-Intervention (6 weeks) and Follow-up (6 months)
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Measure of health status by the EQ-5D-3L questionnaire, consisting of five dimensions (mobility, self-care, usual activities, pain/discomfort, anxiety/depression) each of which can take one of five responses.
The responses record five levels of severity (no problems/slight problems/moderate problems/severe problems/extreme problems).
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Change from Pre-Intervention (baseline) compared to Post-Intervention (6 weeks) and Follow-up (6 months)
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Balance
Time Frame: Change from Pre-Intervention (baseline) compared to Post-Intervention (6 weeks) and Follow-up (6 months)
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Balance Platform, variation of the platform displacement
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Change from Pre-Intervention (baseline) compared to Post-Intervention (6 weeks) and Follow-up (6 months)
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Perception of Recovery
Time Frame: Change from Pre-Intervention (baseline) compared to Post-Intervention (6 weeks) and Follow-up (6 months)
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Perception of Recovery measured by a Global Perceived Effect Scale (11-point scale), ranging from -5 ("much worse"), 0 ("no change"), to 5 ("completely recovered")
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Change from Pre-Intervention (baseline) compared to Post-Intervention (6 weeks) and Follow-up (6 months)
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Rodrigo L Carregaro, PhD, University of Brasilia, School of Physical Therapy
Publications and helpful links
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- COmEBACK Trial
- CAAE68870317.0.0000.8093 (OTHER: Ethics Commitee FCE/UnB)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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