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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02444702
Other study ID # 0006-15-MMC
Secondary ID
Status Recruiting
Phase
First received May 12, 2015
Last updated March 21, 2018
Start date June 15, 2015
Est. completion date December 2018

Study information

Verified date March 2018
Source Meir Medical Center
Contact Shay Shabat, Prof.
Phone 972-9-7471153
Email Shay.Shabat@clalit.org.il
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The long term goal of this project is dual fold. First, the investigators wish to derive, validate and then test the impact of a clinical prediction rule to determine which patients who suffer from CLBP with degenerative changes of the lumbar spine and referred pain to the legs are likely to require surgery and have successful outcomes in the long term. Second, the investigators would like to establish robust methodology and statistical analysis guidelines for creating clinical prediction rules in physical therapy research. This observational cohort project is a first step towards those goals. Here the investigators specifically aim to identify personal, behavioral, psychological, morphological, and physical factors that can predict the need for surgery as well as level of participation restriction in patients who suffer from CLBP with degenerative conditions of the lumbar spine and referred pain to the legs. The investigators will also explore which parameters can predict success after 1 month, 6 and 12 months in patients who underwent decompression/fusion surgery.


Description:

A classification-based approach to identify specific characteristics of patients who seriously suffer from chronic low back pain (CLBP) with referred pain to the legs who are likely to respond to certain interventions has become a research priority in the medical milieu in general and in physical therapy in particularly.While several classifications have been developed to predict success following physical therapy interventions, some have methodological flaws and no clinical prediction rules have been created for patients with CLBP with degenerative changes of the lumbar spine and referred pain to the legs who are likely to require surgery and have successful outcome post-surgery. CLBP is multifactorial and morphological findings such as degenerative changes of the lumbar spine may not explain the phenomenon in full. The international classification of functioning, disability and health allows for a comprehensive description of the patient as a whole and can be used to classify patients according to their anatomy, pathology, impairments and capacity One-hundred and fifty patients who suffer from CLBP with degenerative conditions of the lumbar spine and referred pain to the legs and are candidates for lumbar decompression/fusion surgery will be recruited from a physician office at the Meir medical center, department of orthopaedic surgery, "Kfar-Saba", Israel. The structure and pathology of their lumbar spine will be analyzed in detail from CT and MRI imaging (morphological measurements of their vertebra and the intervertebral discs). Another one-hundred and fifty CT and MRI imaging of non symptomatic low back group will be taken from the "Meir medical center" in order to characterize the symptomatic group and their degenerative changes.


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date December 2018
Est. primary completion date May 2018
Accepts healthy volunteers No
Gender All
Age group 40 Years to 80 Years
Eligibility Inclusion Criteria:

- Participants' diagnosis may include unstable degenerative spondylolisthesis, radicular pain, or documented stenosis with referred pain

Exclusion Criteria:

- Psychiatric illness

- Previous spine surgery

- Painful arthritic hip

- Hospitalization or surgery in the previous 6 months

- Alcohol consumption > 10 drinks/week

- Diabetes or other causes for poly neuropathy

- Metabolic bone disease, tumor, spinal deformity or contraindications to MRI

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Assuta hospital Tel Aviv

Sponsors (1)

Lead Sponsor Collaborator
Meir Medical Center

Country where clinical trial is conducted

Israel, 

References & Publications (11)

Abbas J, Hamoud K, May H, Hay O, Medlej B, Masharawi Y, Peled N, Hershkovitz I. Degenerative lumbar spinal stenosis and lumbar spine configuration. Eur Spine J. 2010 Nov;19(11):1865-73. doi: 10.1007/s00586-010-1516-5. Epub 2010 Jul 21. — View Citation

Ammendolia C, Chow N. Clinical outcomes for neurogenic claudication using a multimodal program for lumbar spinal stenosis: a retrospective study. J Manipulative Physiol Ther. 2015 Mar-Apr;38(3):188-94. doi: 10.1016/j.jmpt.2014.12.006. Epub 2015 Jan 22. — View Citation

Dankaerts W, O'Sullivan PB, Burnett AF, Straker LM. The use of a mechanism-based classification system to evaluate and direct management of a patient with non-specific chronic low back pain and motor control impairment--a case report. Man Ther. 2007 May;12(2):181-91. Epub 2006 Jul 31. — View Citation

Delitto A, Erhard RE, Bowling RW. A treatment-based classification approach to low back syndrome: identifying and staging patients for conservative treatment. Phys Ther. 1995 Jun;75(6):470-85; discussion 485-9. — View Citation

Lubetzky-Vilnai A, Ciol M, McCoy SW. Statistical analysis of clinical prediction rules for rehabilitation interventions: current state of the literature. Arch Phys Med Rehabil. 2014 Jan;95(1):188-96. doi: 10.1016/j.apmr.2013.08.242. Epub 2013 Sep 10. Review. — View Citation

Lundon K, Bolton K. Structure and function of the lumbar intervertebral disk in health, aging, and pathologic conditions. J Orthop Sports Phys Ther. 2001 Jun;31(6):291-303; discussion 304-6. Review. — View Citation

Luoma K, Riihimäki H, Luukkonen R, Raininko R, Viikari-Juntura E, Lamminen A. Low back pain in relation to lumbar disc degeneration. Spine (Phila Pa 1976). 2000 Feb 15;25(4):487-92. — View Citation

Maniadakis N, Gray A. The economic burden of back pain in the UK. Pain. 2000 Jan;84(1):95-103. — View Citation

Masharawi YM, Peleg S, Albert HB, Dar G, Steingberg N, Medlej B, Abbas J, Salame K, Mirovski Y, Peled N, Hershkovitz I. Facet asymmetry in normal vertebral growth: characterization and etiologic theory of scoliosis. Spine (Phila Pa 1976). 2008 Apr 15;33(8):898-902. doi: 10.1097/BRS.0b013e31816b1f83. — View Citation

Matsui H, Maeda A, Tsuji H, Naruse Y. Risk indicators of low back pain among workers in Japan. Association of familial and physical factors with low back pain. Spine (Phila Pa 1976). 1997 Jun 1;22(11):1242-7; discussion 1248. — View Citation

Singh K, Samartzis D, Vaccaro AR, Nassr A, Andersson GB, Yoon ST, Phillips FM, Goldberg EJ, An HS. Congenital lumbar spinal stenosis: a prospective, control-matched, cohort radiographic analysis. Spine J. 2005 Nov-Dec;5(6):615-22. — View Citation

* Note: There are 11 references in allClick here to view all references

Outcome

Type Measure Description Time frame Safety issue
Other Morphological parameters morphological parameters in the lumbar spine will be analyzed from the CT imaging : a) Lumbar lordosis b) Sacral angle orientation, c) Pelvic tilt , d) Pelvis width e) Lumbar vertebral body and disc shape- the vertebral body and inter-vertebral disc lengths, widths, heights and wedging ,Lumbar vertebral arch shape 6 weeks pre-op
Primary The change in Oswestry Disability Index (ODI) score which is equal to or greater than 50% has been used consistently in Physical Therapy literature as the definition of success following an intervention 6 weeks pre-op, 1 month post op, 6 months post op and 1 year post op
Primary The Roland Morris Disability Questionnaire (RMQ) Commonly used in CLBP research as measures of patients' participation restrictions up to 1 year
Secondary The Fear Avoidance Beliefs questionnaire (FABQ) The FABQ was found to be an important prognostic factor for work-related outcomes in patients with sub-acute LBP and a component of clinical predictors rules predicting changes in ODI following physical therapy interventions for patients with LBP 6 weeks pre-op, 1 month post op, 6 months post op and 1 year post op
Secondary The International Physical Activity Questionnaire (IPAQ) The IPAQ was designed to provide a set of well-developed instruments that can be used internationally to obtain comparable estimates of physical activity 6 weeks pre-op, 1 month post op, 6 months post op and 1 year post op
Secondary The Visual Analog Scale (VAS) The VAS is one of the most commonly used pain measures in CLBP research and has been shown to be reliable in this population 6 weeks pre-op, 1 month post op, 6 months post op and 1 year post op
Secondary Lumbar myotomes function Will be taken by the Hand-held dynamometry (HHD) in order to assess the lower extremity muscle force output 6 weeks pre-op, 6 months post op and 1 year post op
Secondary The Long Distance Corridor Walk (LDCW) comprised of a 2 minute warm up and a 400 meter walk as fast as possible 6 weeks pre-op, 6 months post op and 1 year
Secondary The 8 foot up and go The 8-foot version of the Time-up-and-go test is part of the reliable and valid senior fitness test. Performance on the test indicates on sensory, motor, strength and balance function 6 weeks pre-op, 6 months post op and 1 year
Secondary The 30-seconds chair stand test for lower body strength 6 weeks pre-op, 6 months post op and 1 year
Secondary Grip strength Hand grip strength was found to be associated with changes in disability and pain following aquatic therapy in patients with CLBP 6 weeks pre-op, 6 months post op and 1 year
Secondary single leg stance test measures static balance 6 weeks pre-op, 6 months post op and 1 year
Secondary The four square step test measures dynamic balance 6 weeks pre-op, 6 months post op and 1 year
Secondary Passive straight leg raise (PSLR) Passive straight leg raise (PSLR) up to first sensation of pain will be measured with an inclinometer 6 weeks pre-op, 6 months post op and 1 year
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