Manual Physical Therapy and Exercise for Mechanical Neck Disorders
NCT ID: NCT00416117
Last Updated: 2006-12-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE2/PHASE3
100 participants
INTERVENTIONAL
2001-07-31
2004-06-30
Brief Summary
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Detailed Description
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Participants meeting all inclusion criteria were randomized into one of two treatment groups: 1) manual physical therapy and exercise (MTE) or 2) minimal intervention (MI).
Patients in the MTE group received manual physical therapy interventions specifically targeted to impairments identified during the physical examination. Physical therapists chose manual interventions consisting of thrust and non-thrust joint manipulation/mobilization, muscle energy, and soft-tissue mobilization/stretching techniques that are commonly referenced and used in clinical practice. We provided all patients in the MTE group with a standard home exercise program of cervical retraction, deep neck flexor strengthening, and cervical rotation range of motion exercises.
Patients in the MI group received a basic treatment plan consistent with general practitioner care. We provided all patients with a basic regimen of postural advice, encouragement to maintain neck motion and daily activity levels, cervical rotation range of motion exercise, and instructions to continue any prescribed medication use. Minimalist physical therapy treatments consisted of sub-therapeutic pulsed (10%) ultrasound at 0.1w/cm2 for 10 minutes applied to the cervical spine and cervical rotation range of motion exercises. We provided these treatments to maintain the patients' expectations for physical therapy treatment and subsequent improvement, and to standardize the therapist-patient interaction time
The intervention period lasted 3 weeks with both groups receiving treatment twice weekly for up to 6 sessions. We standardized treatment time for both groups by using a one-hour initial evaluation and treatment session and thirty-minute follow-up treatment sessions. Patients did not have to complete all six visits if their symptoms had fully resolved. The treating therapist instructed and supervised all exercises to ensure proper patient technique and understanding.
We collected outcome measure data at baseline and at the patient's 3-week, 6-week and 1-year follow-ups. All outcome measures were collected by physical therapists that were blinded to treatment group allocation.
Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Interventions
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Manual Physical Therapy and Exercise
Minimal Intervention
Eligibility Criteria
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Inclusion Criteria
* age greater than 18
* Neck Disability Index (NDI) score greater than or equal to 10 points
* Composite Visual Analog Scale (VAS) score greater than or equal to 30mm
* Eligible for military health care
* Reside within one hour of the military treatment facilities
* Possess sufficient English language skills to complete all questionnaires
Exclusion Criteria
* history of spinal tumors, spinal infection, cervical spine fracture, or previous neck surgery
* pending legal action regarding their neck pain
* diagnosis of central cervical spinal stenosis
* bilateral upper extremity symptoms
* two positive neurological findings at the same nerve root level
18 Years
ALL
No
Sponsors
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59th Medical Wing
FED
Brooke Army Medical Center
FED
Principal Investigators
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Michael J Walker, PT, DSc
Role: PRINCIPAL_INVESTIGATOR
Brooke Army Medical Center
Locations
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Brooke Army Medical Center
Fort Sam Houston, Texas, United States
Wilford Hall Medical Center
Lackland Air Force Base, Texas, United States
Countries
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References
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Walker MJ, Boyles RE, Young BA, Strunce JB, Garber MB, Whitman JM, Deyle G, Wainner RS. The effectiveness of manual physical therapy and exercise for mechanical neck pain: a randomized clinical trial. Spine (Phila Pa 1976). 2008 Oct 15;33(22):2371-8. doi: 10.1097/BRS.0b013e318183391e.
Other Identifiers
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C.2001.123
Identifier Type: -
Identifier Source: org_study_id