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The Value of Traction in Treatment of Lumbar Radiculopathy

The Value of Traction in Treatment of Lumbar Radiculopathy.

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00942227
Enrollment
120
Registered
2009-07-20
Start date
2009-07-31
Completion date
2012-12-31
Last updated
2013-01-14

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

Conditions

Intervertebral Disk Displacement, Musculoskeletal Diseases, Neuromuscular Diseases, Radiculopathy, Sciatica, Spinal Diseases

Keywords

Sciatica, Radiculopathy, Physical therapy modalities, Rehabilitation

Brief summary

The purpose of this study is to determine the effectiveness of adding mechanical traction to standard physical therapy treatments for patients with low back pain.

Detailed description

Despite the opinions of clinical experts that patients who might benefit from traction may represent distinct sub-groups of patients, most studies have not attempted to narrow their inclusion criteria beyond loose definitions of 'acute' or 'chronic' symptoms. While these studies seem to indicate that traction interventions will be of little benefit when administered to large groups of patients without a prior attempt to select which patients are most likely to benefit, they are not sufficient to preclude the possibility that a subgroup of patients may benefit substantially from the intervention. Recent preliminary studies suggest a there exists a subgroup of patients with LBP that is likely to benefit from traction. The two primary aims of this study are: 1. Determine the validity of the previously-identified prediction criteria to identify patients highly likely to benefit from the addition of traction to a standard physical therapy intervention. 2. Compare the overall effectiveness of addition of a traction component to a standard physical therapy intervention.

Interventions

Extension oriented exercises. Subjects will be instructed in a progression of extension oriented exercises for the lumbar spine

Sponsors

University of Utah
CollaboratorOTHER
59th Medical Wing
CollaboratorFED
Empi, A DJO Company
CollaboratorINDUSTRY
Intermountain Health Care, Inc.
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Chief complaint of pain and/or paresthesia in the lumbar spine with a distribution of symptoms that has extended distal to the gluteal fold on at least one lower extremity within the past 24 hours based on the patient's self-report. * Oswestry disability score of at least 20% * Age at least 18 years and less than 60 years * At least one of the following signs of nerve root compression: 1. Positive ipsilateral or contralateral straight leg raise test (reproduction of leg symptoms with straight leg raise \< 70 degrees) 2. Sensory deficit to pinprick on the ipsilateral lower extremity 3. Diminished strength of a myotome (hip flexion, knee extension, ankle dorsiflexion, great toe extension, or ankle eversion) of the ipsilateral lower extremity 4. Diminished lower extremity reflex (Quadriceps or Achilles) of the symptomatic lower extremity

Exclusion criteria

* Red flags noted in the patient's general medical screening questionnaire (i.e., tumor, metabolic diseases, RA, osteoporosis, spinal compression fracture, prolonged history of steroid use, etc.) * Evidence of central nervous system involvement, to include symptoms of cauda equina syndrome (i.e., loss of bowel/bladder control or saddle region paresthesia) or the presence of pathological reflexes (i.e., positive Babinski) * Patient reports the complete absence of low back and leg symptoms when seated * Recent surgery (\< 6 months) to the lumbar spine or buttocks, or any fusion surgery of the lumbar spine or pelvis * Recent (\< 2 weeks) epidural steroid injection for low back and/or leg pain * Current pregnancy * Inability to comply with the treatment schedule

Design outcomes

Primary

MeasureTime frame
Oswestry Disability IndexBaseline, 6 weeks, 6 months, 1year

Secondary

MeasureTime frame
Global Rating of ChangeBaseline, 6 weeks, 6 months, 1 year

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 31, 2026