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The Value of Traction in the Treatment of Cervical Radiculopathy

The Value of Mechanical Traction in the Treatment of Cervical Radiculopathy

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00979108
Enrollment
86
Registered
2009-09-17
Start date
2009-07-31
Completion date
2013-01-31
Last updated
2014-11-17

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, Neck Pain, Neuromuscular Diseases, Radiculopathy, Spinal Diseases

Keywords

Radiculopathy, Neck pain, 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 neck and arm pain.

Detailed description

Cervical traction is an intervention frequently recommended for the treatment of patients with neck pain. Systematic reviews have not endorsed the use of mechanical traction for patients with neck pain, however these reviews note the poor methodological quality of available research. Trials that have been performed have examined heterogeneous samples of patients with neck pain. It may be that cervical traction has not shown to be effective because only a specific subgroup may benefit from it. Most experts believe that traction is most beneficial for individuals with neck pain extending into the upper extremity who have signs of nerve root compression. Randomized clinical trials examining the effectiveness of traction for patients with these specific characteristics have not been performed. Preliminary studies support the hypothesis that there exists a specific subgroup of patients with neck pain likely to benefit from traction The current study will address 3 important questions: 1. Will the existence of a more specific subgroup of patients who benefit from traction along with a standard exercise program be validated in a second sample of patients? 2. Is cervical traction a critical component of the treatment necessary to maximize outcomes for patients in this subgroup? 3. Do two commonly used traction protocols differ in their effectiveness for patients in this subgroup? (Specifically, we study will compare supine mechanical traction to over-the-door traction.)

Interventions

Mechanical cervical traction will be applied at a moderate force and adjusted based on symptom relief. In addition, subjects will be trained in cervical and postural exercises.

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 70 Years
Healthy volunteers
No

Inclusion criteria

1. Primary complaint of neck pain with symptoms (pain and/or numbness) extending distal to the acromioclavicular joint or caudal to the superior border of the scapula (may be unilateral or bilateral). 2. Age between 18-70 years old 3. Neck Disability Score score \>10 points

Exclusion criteria

1. Red flags indicative of a serious or non-musculoskeletal condition (i.e. tumor, fracture, metabolic diseases, RA, osteoporosis, prolonged history of steroid use, etc.) 2. Diagnosis of cervical spinal stenosis based on CT or MRI imaging 3. Evidence of cervical myelopathy or central nervous system involvement, (e.g., hyperreflexia, intrinsic muscle wasting of the hands, unsteadiness during gait, nystagmus, loss of visual acuity, impaired sensation of the face, altered taste, presence of pathologic reflexes (i.e. positive Hoffman's or Babinski reflex). 4. Prior surgery to the neck or thoracic spine 5. Inability to comply with treatment and follow-up schedule

Design outcomes

Primary

MeasureTime frame
Neck Disability QuestionnaireBaseline, 4 weeks, 6 months, 1year

Secondary

MeasureTime frame
Global Rating of ChangeBaseline, 4 weeks, 6 months, 1 year

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 8, 2026