Recurrent Low Back Pain: Linking Mechanism to Outcomes (RCT)
Primary Purpose
Low Back Pain
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Core Stabilization
Trunk Motion and Fitness
Sponsored by

About this trial
This is an interventional treatment trial for Low Back Pain focused on measuring low back pain, core stabilization, trunk muscle exercises, physical therapy, RCT
Eligibility Criteria
Inclusion Criteria:
- duration of the current episode less than 3 months,
- average pain intensity over past 2 weeks greater than 4 on an 11 point (0 = no pain, 10 = worst pain ever) verbal pain rating scale,
- self-report global function less than 80% (0-100 %, 100% = normal pain free function)
- Oswestry Index > 19%
- no physical therapy or chiropractic treatment for the current episode of low back pain.
- clinical diagnosis of poor trunk control/ clinical lumbar instability needs to be met based upon completion of specific physical therapy examination finding
Exclusion Criteria:
- permanent structural spinal deformity (e.g., scoliosis),
- spinal fracture or history of spinal fracture,
- osteoporosis,
- inflammatory joint disease,
- signs of systemic illness or suspected non-mechanical LBP (spinal tumor or infection),
- previous spinal surgery,
- frank neurological loss, i.e., weakness and sensory loss in a NR distribution,
- pain or paresthesia below the knee,
- leg length discrepancy of greater than 2.5 cm,
- history of neurologic disease that required hospitalization,
- active treatment of another medical illness that would preclude participation in any aspect of the study,
- pregnancy,
- vestibular dysfunction,
- extreme psychosocial involvement
- allergies to medical tape or adhesives
- Body mass index greater than 30 kg/m2
Sites / Locations
- Drexel University Physical Therapy
- Optimum Physical Therapy Associates
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Core Stabilization
Trunk Motion and Fitness
Arm Description
8-week core stabilization program in 3 stage that emphasizes use of specific local trunk stabilizing muscles to restore active control and stability to the trunk. 8-week exercise program, 1-2 sessions/ week, 30-60 minute sessions
8-week exercise program in 3 stages emphasizing spine motion, general trunk flexibility and strengthening and cardiovascular fitness. 8-week exercise program, 1-2 sessions/ week, 30-60 minute sessions
Outcomes
Primary Outcome Measures
Trunk Neuromuscular Control
Using surface EMG, kinematics and force parameters. Trunk neuromuscular control is characterized and compared between groups and pre/post intervention.
Secondary Outcome Measures
Clinical Outcomes
Oswestry Disability Index- measure of self-perceived functional limitations NPRS- numeric pain index
Full Information
NCT ID
NCT01360359
First Posted
May 24, 2011
Last Updated
March 9, 2015
Sponsor
Drexel University
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
1. Study Identification
Unique Protocol Identification Number
NCT01360359
Brief Title
Recurrent Low Back Pain: Linking Mechanism to Outcomes (RCT)
Official Title
Recurrent Low Back Pain: Linking Mechanism to Outcomes (RCT)
Study Type
Interventional
2. Study Status
Record Verification Date
March 2015
Overall Recruitment Status
Completed
Study Start Date
May 2011 (undefined)
Primary Completion Date
March 2015 (Actual)
Study Completion Date
March 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Drexel University
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this randomized clinical trial of low back pain exercise programs is to determine if trunk control can be changed by core stabilization exercises. The proposed mechanism of pain reduction and functional improvement of core stabilization exercises is that it enhances trunk movement and muscle control. This study will provide preliminary evidence of the link between patient outcomes and treatment mechanisms.
The investigators hypothesize that:
both treatment groups will demonstrate significant improvements in pain and function;
only subjects in the core stabilization group will demonstrate significant improvements in trunk movement and muscle control.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Low Back Pain
Keywords
low back pain, core stabilization, trunk muscle exercises, physical therapy, RCT
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
17 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Core Stabilization
Arm Type
Experimental
Arm Description
8-week core stabilization program in 3 stage that emphasizes use of specific local trunk stabilizing muscles to restore active control and stability to the trunk.
8-week exercise program, 1-2 sessions/ week, 30-60 minute sessions
Arm Title
Trunk Motion and Fitness
Arm Type
Active Comparator
Arm Description
8-week exercise program in 3 stages emphasizing spine motion, general trunk flexibility and strengthening and cardiovascular fitness.
8-week exercise program, 1-2 sessions/ week, 30-60 minute sessions
Intervention Type
Other
Intervention Name(s)
Core Stabilization
Intervention Description
3 Stages: Stage 1: emphasis on neutral spine position, co-contraction of stabilizing muscles with performance feedback through observation and palpation for correct muscle activation; patient education
Stage 2: promotes maintenance of co-contraction while performing movements of the arms/legs and trunk progressing to preformance of these exercises on unstable surfaces; trunk muscle conditioning also emphasized; feedback gradually reduced.
Stage 3: emphasis on maintenance of co-contraction while performing functional activities; stable and unstable surfaces; use of perturbation and random practice to enhance motor learning.
Intervention Type
Other
Intervention Name(s)
Trunk Motion and Fitness
Intervention Description
3 Stages: Stage 1: reducing pain and restoring spine motion and flexibility; patient education
Stage 2: trunk muscle conditioning exercises
Stage 3: trunk muscle conditioning and cardiovascular conditioning exercises
Primary Outcome Measure Information:
Title
Trunk Neuromuscular Control
Description
Using surface EMG, kinematics and force parameters. Trunk neuromuscular control is characterized and compared between groups and pre/post intervention.
Time Frame
Baseline, 8 weeks
Secondary Outcome Measure Information:
Title
Clinical Outcomes
Description
Oswestry Disability Index- measure of self-perceived functional limitations NPRS- numeric pain index
Time Frame
Baseline, 8-weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
duration of the current episode less than 3 months,
average pain intensity over past 2 weeks greater than 4 on an 11 point (0 = no pain, 10 = worst pain ever) verbal pain rating scale,
self-report global function less than 80% (0-100 %, 100% = normal pain free function)
Oswestry Index > 19%
no physical therapy or chiropractic treatment for the current episode of low back pain.
clinical diagnosis of poor trunk control/ clinical lumbar instability needs to be met based upon completion of specific physical therapy examination finding
Exclusion Criteria:
permanent structural spinal deformity (e.g., scoliosis),
spinal fracture or history of spinal fracture,
osteoporosis,
inflammatory joint disease,
signs of systemic illness or suspected non-mechanical LBP (spinal tumor or infection),
previous spinal surgery,
frank neurological loss, i.e., weakness and sensory loss in a NR distribution,
pain or paresthesia below the knee,
leg length discrepancy of greater than 2.5 cm,
history of neurologic disease that required hospitalization,
active treatment of another medical illness that would preclude participation in any aspect of the study,
pregnancy,
vestibular dysfunction,
extreme psychosocial involvement
allergies to medical tape or adhesives
Body mass index greater than 30 kg/m2
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sheri P. Silfies, PT, PhD
Organizational Affiliation
Drexel University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Drexel University Physical Therapy
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19102
Country
United States
Facility Name
Optimum Physical Therapy Associates
City
West Chester
State/Province
Pennsylvania
ZIP/Postal Code
19380
Country
United States
12. IPD Sharing Statement
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Recurrent Low Back Pain: Linking Mechanism to Outcomes (RCT)
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