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Low Back PainNCT02060617

A Comparison of Two Different Methods of Physical Therapy to Treat Acute and Subacute Low Back Pain

A study testing Patient Education, Manual therapy of the thoracolumbosacral spine and hips and Treatment-Based Classification intervention in people with Low Back Pain, run by Hendricks Regional Health at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Recent research has shown that classifying patients with low back pain into treatment subgroups results in better improvements than treating all patients with low back pain the same. However, physical therapists may use different types of information to determine how to classify their patients. Read more about this study

Who is it for?
Ages 18 to 80 years
Conditions the study is for
Low Back Pain
What is being tested?
Patient Education, Manual therapy of the thoracolumbosacral spine and hips and Treatment-Based Classification intervention
Could I receive a placebo?
No, everyone receives an active treatment
How many people
23 participants
Where
1 siteUnited States
Study dates
Apr 2014to Sep 2016
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • primary complaint of low back pain with or without leg symptoms
  • duration of symptoms 24 hours to 90 days
  • modified Oswestry score of 20 or greater
  • able to read and speak English.

Who cannot join

  • current pregnancy
  • spinal steroid injections within the past month
  • spinal surgery in the past 6 months
  • current worker's compensation or motor vehicle accident claim
  • presence of any red flag symptoms indicating possible serious pathology or non-musculoskeletal pain

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Hendricks Regional Health

    Plainfield, Indiana, 46168

Other trials in United States

About this study

Official title: Impairment-Based Versus Classification-Based Physical Therapy for Acute and Subacute Low Back Pain: a Randomized Controlled Trial

Recent research has shown that classifying patients with low back pain into treatment subgroups results in better improvements than treating all patients with low back pain the same. However, physical therapists may use different types of information to determine how to classify their patients. One method uses patient characteristics that have been shown by research to predict good results from a certain type of treatment. Another method uses specific impairments that the physical therapist identifies in a clinical exam to determine which treatment to provide. It is not currently known if one of these methods is better than the other. The purpose of this study is to determine if research-based classification or impairment-based treatment is more effective for treating patients with low back pain that has lasted less than 90 days in terms of improvements in pain and disability. The results of this study may help reduce the high financial cost associated with low back pain.

Read the detailed description

PURPOSE: The purpose of this study is to describe a multimodal impairment-based clinical model for the treatment of low back pain utilizing the concept of Regional Interdependence (Wainner et al 2007) and to determine the relative effectiveness of this model versus classification-based therapy using the Treatment-Based Classification System for acute and subacute low back pain (Delitto et al 1995, Fritz et al 2006, Fritz et al 2007) in terms of improvements in pain and disability at 4 weeks and 6 months.

BACKGROUND: Recent studies have shown that subclassifying patients with low back pain into treatment groups results in better outcomes than treating all patients with low back pain as homogenous groups. (Fritz et al 2003) However, no studies have directly compared the efficacy of impairment-based versus classification-based physical therapy for patients with acute and subacute low back pain.

HYPOTHESIS: We suspect that both methods of treatment will be effective, but we are uncertain if one will be more effective than the other. Therefore, our null hypothesis will be that both methods will be equally effective.

METHODS:

  1. Patients referred to physical therapy at Hendricks Regional Health in Plainfield, IN will be screened for eligibility. Eligible participants will be offered the opportunity to voluntarily participate in the research study. Those patients who are both eligible and interested will receive an informed consent form approved by the Hendricks Regional Health Institutional Review Board.
  2. All subjects will complete a standard intake form and self-report measures. The principal investigator will obtain a subjective history from the patient and perform a standardized baseline physical examination.
  3. After the baseline examination, subjects will be randomized in blocks of 4, 6, or 8 using a concealed, computer-generated randomization sequence accessed electronically through a Microsoft Excel spreadsheet using the VLOOKUP function to return the group assignment when the subject number is entered.
  4. All subjects in both groups will be treated by the principal investigator two times per week for two weeks followed by once per week for two weeks (total of 6 visits) regardless of treatment group assignment. All subjects will receive standardized education as well as additional individualized education as deemed appropriate by the treating clinician. Subjects will be given a home exercise program consisting of the same exercises they performed in physical therapy and asked to perform their exercises twice per day.
  5. Patients in the impairment-based group will be treated using a multi-modal treatment approach utilizing manual therapy of the thoracolumbosacral spine and hip as well as motor control exercises. Patients in the classification-based group will be categorized into subgroups according to the previously described Treatment-Based Classification (TBC) Algorithm and treated accordingly.
  6. After completion of the 6 visits, we intend to discharge most patients to a home exercise program. However, patients who require more or fewer visits than this will still be included in the intention-to-treat analysis. Patients will be encouraged to perform their home exercises at least 3 times per week until the 6 month follow up.
  7. Primary and secondary outcome measures will be collected at 4 weeks and 6 months from baseline.

DATA ANALYSIS:

Study data will be analyzed using SPSS Statistical Software (IBM, Armonk, NY).

  1. Baseline characteristics will be examined for between group differences.
  2. Primary outcomes will be analyzed using a repeated measures analysis of co-variance (ANCOVA) to examine a group x time interaction for pain and disability at baseline, 4 weeks, and 6 months controlling for baseline covariates of Fear Avoidance Behavior Questionnaire physical activity subscale score (FABQpa), duration of symptoms, and prior history of low back pain. Median and range values will be calculated for Global Rating of Change at 4 weeks and 6 month. Primary outcome measures will also be dichotomized and combined in order to determine overall treatment success for the 4 week and 6 month follow ups.
  3. Intention-to-treat analysis using multiple imputation to account for missing values will be used in all analyses. A secondary per-protocol analysis will be performed for patients who completed exactly 6 visits, performed their home exercise program at least 6 times per week, and completed all outcomes at all time points.
Conditions
Low Back Pain
Being tested
Patient Education, Manual therapy of the thoracolumbosacral spine and hips, Motor control exercises, Treatment-Based Classification intervention
Keywords
low back pain, physical therapy, manual therapy, manipulation, exercise, motor control, regional interdependence
Medical subject headings
Low Back Pain, Motor Activity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Patient EducationBehavioural

    All subjects will receive education that back pain is common but rarely harmful in nature, that pain does not necessarily mean that there is structural damage to their back, and that they should try to remain as active as they are able within the limits of their pain. In addition, individualized education regarding posture, body mechanics, sleeping positions, or other concerns of the patient will be provided on a pragmatic basis as deemed appropriate by the treating clinician.

  • Manual therapy of the thoracolumbosacral spine and hipsProcedure or surgery

    Thrust and/or non-thrust manipulation and soft tissue mobilization as determined by mobility impairments identified on clinical examination.

  • Motor control exercisesProcedure or surgery

    Motor control exercises as determined by motor control impairments identified on clinical examination.

  • Treatment-Based Classification interventionProcedure or surgery

    Lumbopelvic manipulation and range of motion exercise, spinal stabilization exercises, direction specific exercises, and/or traction will be applied as determined by the Treatment-Based Classification (TBC) Algorithm.

Study groups in NCT02060617
Study groupRoleWhat they receive
Impairment-Based GroupExperimentalThe impairment-based intervention will be a multi-modal treatment approach utilizing manual therapy of the thoracolumbosacral spine and hips as well as motor control exercises. Patient education will also be provided.
Receives: Behavioral: Patient Education; Procedure: Manual therapy of the thoracolumbosacral spine and hips; Procedure: Motor control exercises
Classification-Based GroupActive comparatorPatients in this group will be categorized into subgroups according to the Treatment-Based Classification (TBC) Algorithm and treated accordingly. Patient education will also be provided.
Receives: Behavioral: Patient Education; Procedure: Treatment-Based Classification intervention

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in Modified Oswestry Disability Questionnaire (ODQ) score

    A measure of self-reported disability with scores ranging from 0% to 100% disability.

    Measured: Baseline, 4 weeks, 6 months

Secondary outcomes (3)
  1. Change in Numeric Pain Rating Scale (NPRS) score

    An 11 point scale in which patients rate their pain numerically with "0" representing no pain and "10" representing excruciating pain.

    Measured: Baseline, 4 weeks, 6 months

  2. Global Rating of Change (GRC)

    A self-report measure that asks subjects to rate the change in their symptoms from baseline. Scores range from +7 ("a very great deal better") to -7 ("a very great deal worse") with 0 representing no change.

    Measured: 4 weeks, 6 months

  3. Overall Treatment Success

    Success will be defined as a 50% or greater improvement in modified Oswestry Disability Questionnaire score, a decrease in Numeric Pain Rating Scale score of 3.5 points or greater, and Global Rating of Change score of +5 ("quite a bit better") or greater. If all three of these criteria are met, the overall outcome will be considered "successful". If one or more of these criteria is not met, overall outcome will be considered "unsuccessful".

    Measured: 4 weeks, 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted12 Feb 2014 (estimated)
  2. Study startApr 2014
  3. Primary completionApr 2016
  4. Study completionSep 2016

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
23 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02060617
Sponsor's protocol ID
13-7
Status last verified
Sep 2016
First submitted
1 Dec 2013
Last updated
29 Sep 2016
Results posted
No
Data monitoring committee
No

Publications

  • Delitto A, Erhard RE, Bowling RW. A treatment-based classification approach to low back syndrome: identifying and staging patients for conservative treatment. Phys Ther. 1995 Jun;75(6):470-85; discussion 485-9. doi: 10.1093/ptj/75.6.470.

    PubMed 7770494
  • Fritz JM, Brennan GP, Clifford SN, Hunter SJ, Thackeray A. An examination of the reliability of a classification algorithm for subgrouping patients with low back pain. Spine (Phila Pa 1976). 2006 Jan 1;31(1):77-82. doi: 10.1097/01.brs.0000193898.14803.8a.

    PubMed 16395181
  • Fritz JM, Cleland JA, Childs JD. Subgrouping patients with low back pain: evolution of a classification approach to physical therapy. J Orthop Sports Phys Ther. 2007 Jun;37(6):290-302. doi: 10.2519/jospt.2007.2498.

    PubMed 17612355
  • Wainner RS, Whitman JM, Cleland JA, Flynn TW. Regional interdependence: a musculoskeletal examination model whose time has come. J Orthop Sports Phys Ther. 2007 Nov;37(11):658-60. doi: 10.2519/jospt.2007.0110. No abstract available.

    PubMed 18057674
  • Fritz JM, Delitto A, Erhard RE. Comparison of classification-based physical therapy with therapy based on clinical practice guidelines for patients with acute low back pain: a randomized clinical trial. Spine (Phila Pa 1976). 2003 Jul 1;28(13):1363-71; discussion 1372. doi: 10.1097/01.BRS.0000067115.61673.FF.

    PubMed 12838091

Questions about this trial

What is this clinical trial studying?

A study testing Patient Education, Manual therapy of the thoracolumbosacral spine and hips and Treatment-Based Classification intervention in people with Low Back Pain, run by Hendricks Regional Health at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 29 Sep 2016. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in Modified Oswestry Disability Questionnaire (ODQ) score (time frame: Baseline, 4 weeks, 6 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02060617, which also lists 5 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Sep 2016.

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