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Thrust Manipulation Versus Non-Thrust Manipulation

Phase 2
Completed
Conditions
Mechanical Low Back Pain
Interventions
Procedure: Non-thrust manipulation
Procedure: Thrust manipulation
Registration Number
NCT01438203
Lead Sponsor
Walsh University
Brief Summary

The objective of this study is to investigate the comparative benefit of thrust and non-thrust manipulation on a population of patients with low back pain. The investigators hypothesize that there will be no difference in 4 week outcomes or greater, between the two groups.

Detailed Description

Thrust manipulation is considered traditional spinal manipulation. Nonthrust manipulation is considered mobilization. The mobilization will be used in a similar manner as in clinical practice and this differs from past studies.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
149
Inclusion Criteria
  • Patients, age 18 and older, with mechanically producible low back pain, who attend care at a physical therapy outpatient setting, will be screened for eligibility for the study.
  • For patients to meet inclusion requirements, they had to display a within session change in pain and/or range of motion during the assessment phase of the clinical examination. In other words, as the clinician performed their assessment and applied a passive accessory assessment technique, the pain and/or range of motion improved during that session, which suggests a favorable outcome using a comparable treatment technique. This is hallmark clinical finding in the patient response model and has been proposed as both a predictor of a positive outcome and as a prognostic variable toward long-term improvements in impairments.
Exclusion Criteria
  • The presence of any red flags (i.e., tumor, metabolic diseases, RA, osteoporosis, prolonged history of steroid use, etc.)
  • Signs consistent with nerve root compression (reproduction of low back or leg pain with straight leg raise at less than 45°
  • Muscle weakness involving a major muscle group of the lower extremity,
  • Diminished lower extremity muscle stretch reflex
  • Diminished or absent sensation to pinprick in any lower extremity dermatome)
  • Other exclusion criteria included prior surgery to the lumbar spine and current pregnancy

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Non-thrust manipulationNon-thrust manipulationClinicians will apply non-thrust manipulation (targeted) as performed in a clinical manner for treatment for included individuals
Thrust manipulationThrust manipulationClinicians will use thrust manipulation at a targeted level to provide the treatment on selected individuals
Primary Outcome Measures
NameTimeMethod
Oswestry disability indexBaseline to discharge from therapy services (up to 4 months). An expected average is 4 weeks.

Change score

Secondary Outcome Measures
NameTimeMethod
Numeric Pain Rating Scale (NPRS)Baseline to discharge from therapy services (up to 4 months). An expected average is 4 weeks.

Change score

Trial Locations

Locations (1)

Walsh University

🇺🇸

North Canton, Ohio, United States

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