Effectiveness of Fascial Manipulation for Chronic Low Back Pain
Recruitment status was Recruiting
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Purpose
The purpose is to evaluate the effectiveness of a physiotherapy program for chronic low back pain. We'll randomize more about 35 patients in two groups. Both groups will receive an 8 physioterapy intervention in 4 weeks, in particular the first group (study) will receive 4 Fascial Manipulation treatment combined with 4 session of a standard approach (mobilization and stretching exercises); whereas the second (control) will receive only the standard approach.
| Condition | Intervention |
|---|---|
|
Low Back Pain |
Other: Fascial Manipulation |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Single Blind (Outcomes Assessor) Primary Purpose: Treatment |
| Official Title: | Effectiveness of Fascial Manipulation for Chronic Low Back Pain. A Randomized Controlled Trial |
- disabilty level, evaluated with the Roland and Morris Disability Questionnaire [ Time Frame: from the first evaluation, at the end of the treatment ] [ Designated as safety issue: No ]we'll compare the baseline data (the first evaluation), with data at the end of the treatment, and with at every fullow up (30 and 90 days from the end of the treatment)
- pain and social activity level evaluated with Brief Pain Inventory. [ Time Frame: from the first evaluation, at the end of the treatment ] [ Designated as safety issue: No ]we'll compare the baseline data (the first evaluation), with data at the end of the treatment, and with at every fullow up (30 and 90 days from the end of the treatment)
- quality of life, evaluated with SF-36 [ Time Frame: from the first evaluation, at the end of the treatment ] [ Designated as safety issue: No ]we'll compare the baseline data (the first evaluation), with data at the end of the treatment, and with at every fullow up (30 and 90 days from the end of the treatment)
- pain, assessed with visual analogical scale [ Time Frame: at the first evaluation, at the end of the treatment ] [ Designated as safety issue: No ]we'll compare the baseline data (the first evaluation), with data at the end of the treatment, and with at every fullow up (30 and 90 days from the end of the treatment)
| Estimated Enrollment: | 50 |
| Study Start Date: | April 2009 |
| Estimated Study Completion Date: | December 2010 |
| Estimated Primary Completion Date: | December 2009 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: fascial manipolation
8 treatment sessions: 4 of fascial manipulation treatment, and 4 of standard physiotherapy (rexing exercise, stretching, abdominal and paravertebral isometric muscular recruiting)
|
Other: Fascial Manipulation
8 treatment session in 4 weeks: every week both fascial manipulation and standard physiotherapy
Other Names:
|
|
Active Comparator: physiotherapy
8 treatment sessions of standard physiotherapy (rexing exercise, stretching, abdominal and paravertebral isometric muscular recruiting)
|
Other: Fascial Manipulation
8 treatment session in 4 weeks: every week both fascial manipulation and standard physiotherapy
Other Names:
|
Detailed Description:
All patients were assessed and randomised by a physician. The control group intervention concerned of: relaxation of lumbar and respiration muscles, stretching for posterior muscular chain and hip flexors, assisted/active mobilization of lumbar region in sagittal plane and rotation, exercises to improve proprioception of lumbar spine, active and progressive movement of lumbar spine in anterior flexion, extension, lateroflexion and rotation, active exercise for lumbar stabilizers muscles, occupational training for activity of daily living, indications and recommendations for correct postures. The study group intervention received 4 manual intervention on deep fascial tissues, according to fascial manipulation tecnique, providing a specific motor and manual assessment, and a deep manual intervention over specific fascial alteration.
Eligibility| Ages Eligible for Study: | 20 Years to 60 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- patients with a chronic low back pain (more than 7 weeks)
- age between 20 to 60 years old
Exclusion Criteria:
- presence of neurological red flags
- continuative assumption of drugs for low back pain
- no positive imaging for spine lesions (fractures, spondilolistesi,
- vascular desease (aneurism abdominal aorta)
- secondary lesions (oncological desease)
- rheumatic systemic desease
- any other neurological desease which could compromise the partecipation to the program exercise
Contacts and Locations| Contact: Mirco Branchini | +393394458374 | mirco.branchini@gmail.com |
| Contact: Francesca Lopopolo | +393494373497 | francesca.lopopolo@gmail.com |
| Italy | |
| Universitary Hospital of Bologna - S.Orsola Malpighi | Recruiting |
| Bologna, Italy, 40138 | |
| Contact: mirco branchini, Ph. +393394458374 mirco.branchini@gmail.com | |
| Contact: francesca lopopolo, ph. francesca.lopopolo@gmail.com | |
| Principal Investigator: Mirco Branchini, Ph. | |
| Study Director: | Mirco Branchini, Ph. | University of Bologna - Degree course in Physioterapy |
More Information
Additional Information:
Publications:
| Responsible Party: | Mirco Branchini - Dr. Physioterapist, Degree Course in Physiotherapy - University of Bologna |
| ClinicalTrials.gov Identifier: | NCT01269983 History of Changes |
| Other Study ID Numbers: | CdL_Ft_lombalgia_09 |
| Study First Received: | January 3, 2011 |
| Last Updated: | January 4, 2011 |
| Health Authority: | Italy: Ethics Committee |
Keywords provided by University of Bologna:
|
low back pain fascial manipulation physioterapy physical activity |
Additional relevant MeSH terms:
|
Back Pain Low Back Pain Pain |
Neurologic Manifestations Nervous System Diseases Signs and Symptoms |
ClinicalTrials.gov processed this record on June 17, 2013