- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04394494
RCT of Motor Imagery of Extension for LBP vs. Exercise
A Randomized Clinical Trial of Extension for Low Back Pain: Motor Imagery of Extension Versus Physical Extension Exercises
Low back pain (LBP) is the most common musculoskeletal condition treated in physical therapy, accounting for an estimated 25-40% of outpatient physical therapy visits. One strategy commonly used for treating LBP is directional preference. Directional preference is the process of examining a patient with LBP's response to a movement direction, i.e., extension, and if it coincides with improvement, the test becomes part of the treatment. Various studies have shown evidence for, and use of directional preference by physical therapists. Specifically for LBP, directional preference usually involves either an extension-bias or flexion-bias, with various studies indication an extension protocol being the most common (estimated > 80% of patients). With extension exercises, a favorable therapeutic effect result in centralization of symptoms (leg pain migrates proximal), improved range of motion (ROM), decreased pain and decreased fear of movement.
In recent years there has been an increased interest in various pain neuroscience strategies to help people in pain, including LBP. It is well established that the physical body of a person is represented in the brain by a network of neurons, often referred to as a representation of that particular body part in the brain. This representation refers to the pattern of activity that is evoked when a particular body part is stimulated. The most famous area of the brain associated with representation is the primary somatosensory cortex (S1). These neuronal representations of body parts are dynamically maintained. It has been shown that patients with pain display different S1 representations than people with no pain. The interesting phenomenon associated with cortical restructuring is the fact that the body maps expand or contract, in essence increasing or decreasing the body map representation in the brain. Furthermore, these changes in shape and size of body maps seem to correlate to increased pain and disability. Various studies have shown that physical movement is associated with restoring the cortical maps, which in turn may be associated with a decreased pain experience.
In patients with high levels of pain, sensitization of the nervous system and fear of movement, physical movement itself may increase a pain experience. An added therapeutic ability to help restore these cortical maps is motor imagery (visualization). Various studies have shown that motor imagery activate the same areas of the brain as when actually physically moving, thus restoring the altered maps "without moving."
Study Overview
Status
Conditions
Detailed Description
- Patient arrive to physical therapy with low back pain (physician referral or self-referral)
- Patient complete standard clinic medical and insurance intake forms
- Based on the intake forms, patients are screened by the physical therapists against the inclusion criteria and if met, asked to participate in the study
- Upon agreement, a written consent is signed
Patients complete research intake forms:
- Demographic information
- Age
- Gender
- Duration of LBP
Location of LBP (body chart with grid allocation)
- Pain rating (NPRS): Numeric Pain Rating Scale
- Fear-Avoidance (Physical and Work Subscales) (FABQ)
- Pain Catastrophization Scale (PCS)
- Patients undergo a standard physical therapy interview
- Patients undergo a standard physical therapy examination
- Patients undergo a directional preference test to determine if they are potentially responsive to extension exercises
- Once patients are shown to be responsive to extension, they are alternately allocated to receive motor imagery of extension exercises (experimental group; [EG]) or physical extension exercises (control group, [CG]).
- Prior to the treatment lumbar extension ROM will be measured via a standardized procedure
- Upon completion of the tests, patients will receive one of two allocated treatments
Following the treatment, patients will undergo repeat measures of:
- Spinal extension ROM
- Pain rating
- Fear of movement
- Pain catastrophization Patients will be asked to return to physical therapy in 2 to 3 days (standard care)
Upon return, measurements will be repeated of:
- Pain rating
- Fear of movement
- Pain catastrophization
- Spinal extension ROM This marks the end of data collection (and study) of the individual patient - Following the tests the patient is treated per the discretion of the therapist as the data collection has been completed
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Illinois
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Naperville, Illinois, United States, 60517
- Edward Elmhurst Health Physical Therapy
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Iowa
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Davenport, Iowa, United States, 52807
- Genesis Physical Therapy - 53rd St
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Davenport, Iowa, United States, 52803
- Kevin Farrell
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Davenport, Iowa, United States, 52806
- Rock Valley Physical Therapy
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- LBP of less than 3 months duration
- Age 18-65
- Able to read and understand English
- Fit directional preference of extension
Exclusion Criteria:
- Any red flags for therapy
- Prior spinal surgery
- Directional preference of flexsion
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: Motor Imagery
Patients are instructed in a motor imagery protocol of imaging extension exercises (similar to the CG), without doing the actual extension exercises.
Patients will be instructed in visualizing them moving into extension and back as well as common sensations they may experience (as if doing the actual exercise).
They will repeat the visualization process 10 times while in the clinic, after which they will be instructed in a home program containing the same treatment - every 2 hours, perform 10 visualization exercises.
|
This study will compare imagining doing specific extension based exercises for LBP vs. actually performing the exercises.
This intervention will be just imaging doing the exercises.
|
ACTIVE_COMPARATOR: Control
Patients are instructed in extension exercises and actually, physically doing the actual extension exercises.
Patients will physically repeat the extension exercises 10 times while in the clinic, after which they will be instructed in a home program containing the same treatment - every 2 hours, perform 10 exercises.
|
This study will compare imagining doing specific extension based exercises for LBP vs. actually doing them.
This intervention will be actually, physically performing the exercises.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Spine ROM
Time Frame: within a single, 90 minute session
|
range patient is able to bend backward
|
within a single, 90 minute session
|
Pain rating
Time Frame: within a single, 90 minute session
|
Numeric pain rating Scale 0 - 10 (0 = no pain and 10 = worst pain).
The minimal detectable change (MDC) for the NPRS for low back pain is reported to be 2.0.
|
within a single, 90 minute session
|
Fear of Movement
Time Frame: within a single, 90 minute session
|
Fear Avoidance Belief Questionnaire (FABQ): The FABQ is a self-report of patients feelings about their fear to move.
|
within a single, 90 minute session
|
Pain Catastrophization
Time Frame: within a single, 90 minute session
|
Pain Catastrophization Scale: The PCS is a self-report questionnaire assessing inappropriate coping strategies and catastrophic thinking about pain and injury.
on a 13-item, 5-point Likert scale with higher scores indicating elevated levels of catastrophizing.
|
within a single, 90 minute session
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SAU McKenzie MI
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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