Skip to main content
Clinical Trials/NCT00916734
NCT00916734
Completed
Phase 3

Assessing Patient Response to Therapeutic Exercise Based on the Clinical Prediction Rule for Spinal Manipulation

Daemen College1 site in 1 country31 target enrollmentNovember 2007
ConditionsLow Back Pain

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Low Back Pain
Sponsor
Daemen College
Enrollment
31
Locations
1
Primary Endpoint
Pain level as measured on numerical pain rating scale
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

The purpose of this study is to determine whether patients who meet the criteria of the clinical prediction rule for spinal manipulation may respond more favorably to repeated exercises according to a direction of preference (what makes the symptoms decrease). The investigators do not know which of these two commonly-used treatments (manipulation or specific exercise) is better to treat low back pain.

Detailed Description

With the trends in health care focusing on treatment effectiveness, it is important for physical therapists to select the most appropriate intervention according to patient classification. Physical therapy interventions for management of LBP include therapeutic exercises and spinal manipulation. The purpose of this study is to determine whether patients who fit the Clinical Prediction Rule (CPR) for spinal manipulation may respond instead to exercise according to repeated lumbar movements in the direction of preference. The subjects for this study will be comprised of individuals referred for treatment of low back pain and data will be collected by physical therapists with certification in MDT who had experience treating patients through the use of spinal manipulation. Patient functional questionnaires and impairment measures will be used to analyze the patient's perceived level of function and outcome. Following the completion of an informed consent, subjects will undergo a physical therapy examination by a licensed physical therapist. Patients will be included in the study if they meet the CPR for spinal manipulation as describe in earlier research 6,11. Following the examination, all qualified subjects will be randomly assigned to either the (1) spinal manipulation group or (2) the McKenzie (MDT) group and will receive treatment in accordance with their assigned group. The assessment tools administered at the initial examination will be readministered for follow-up analysis.

Registry
clinicaltrials.gov
Start Date
November 2007
End Date
December 2009
Last Updated
14 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
Daemen College
Responsible Party
Principal Investigator
Principal Investigator

Ronald J. Schenk

Associate Professor Physical Therapy

Daemen College

Eligibility Criteria

Inclusion Criteria

  • people who meet the clinical prediction rule for spinal manipulation

Exclusion Criteria

  • people receiving worker's compensation
  • those who have had spinal surgery

Outcomes

Primary Outcomes

Pain level as measured on numerical pain rating scale

Time Frame: 1 year

Secondary Outcomes

  • Oswestry score(1 year)

Study Sites (1)

Loading locations...

Similar Trials