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Clinical, Morphological and Functional Success Predictors Following Lumbar Spinal Surgery in Patients With Chronic Low Back Pain and Degenerative Disorders.

Clinical, Morphological and Functional Success Predictors Following Lumbar Spinal Surgery in Patients With Chronic Low Back Pain and Degenerative Disorders.

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02444702
Enrollment
200
Registered
2015-05-14
Start date
2015-06-15
Completion date
2018-12-31
Last updated
2018-03-22

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

Conditions

Low Back Pain

Keywords

spinal stenosis, clinical predictors rules, MRI, fusion, low back pain

Brief 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.

Detailed 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.

Interventions

None listed

Sponsors

Meir Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
40 Years to 80 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
The Roland Morris Disability Questionnaire (RMQ)up to 1 yearCommonly used in CLBP research as measures of patients' participation restrictions
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 intervention6 weeks pre-op, 1 month post op, 6 months post op and 1 year post op

Secondary

MeasureTime frameDescription
The International Physical Activity Questionnaire (IPAQ)6 weeks pre-op, 1 month post op, 6 months post op and 1 year post opThe IPAQ was designed to provide a set of well-developed instruments that can be used internationally to obtain comparable estimates of physical activity
The Visual Analog Scale (VAS)6 weeks pre-op, 1 month post op, 6 months post op and 1 year post opThe VAS is one of the most commonly used pain measures in CLBP research and has been shown to be reliable in this population
Lumbar myotomes function6 weeks pre-op, 6 months post op and 1 year post opWill be taken by the Hand-held dynamometry (HHD) in order to assess the lower extremity muscle force output
The Long Distance Corridor Walk (LDCW)6 weeks pre-op, 6 months post op and 1 yearcomprised of a 2 minute warm up and a 400 meter walk as fast as possible
The 8 foot up and go6 weeks pre-op, 6 months post op and 1 yearThe 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
Grip strength6 weeks pre-op, 6 months post op and 1 yearHand grip strength was found to be associated with changes in disability and pain following aquatic therapy in patients with CLBP
single leg stance test6 weeks pre-op, 6 months post op and 1 yearmeasures static balance
The four square step test6 weeks pre-op, 6 months post op and 1 yearmeasures dynamic balance
Passive straight leg raise (PSLR)6 weeks pre-op, 6 months post op and 1 yearPassive straight leg raise (PSLR) up to first sensation of pain will be measured with an inclinometer
The 30-seconds chair stand test6 weeks pre-op, 6 months post op and 1 yearfor lower body strength
The Fear Avoidance Beliefs questionnaire (FABQ)6 weeks pre-op, 1 month post op, 6 months post op and 1 year post opThe 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

Other

MeasureTime frameDescription
Morphological parameters6 weeks pre-opmorphological 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

Countries

Israel

Contacts

Primary ContactShay Shabat, Prof.
Shay.Shabat@clalit.org.il972-9-7471153
Backup ContactAvihai Soroka, MscPT
yossefm@post.tau.ac.il972-522982802

Outcome results

None listed

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