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TerminatedNCT03065894Updated Sep 7, 2018

Risk Stratification in Primary Care Combined With Stratified-specific Physical Therapy Care for Low Back Pain

An interventional study of Matched Physical Therapy Intervention and Current Care in Family Medicine in Low Back Pain, sponsored by University of Vermont Medical Center. Terminated at 1 site in United States. Open to participants aged 21 Years to 60 Years. Per ClinicalTrials.gov, last updated 2018-09-07.

Sponsored by University of Vermont Medical Center · Not applicable, Interventional, and Treatment

Why this study was terminated
Lack of subject enrollment
Phase
Not applicable
Study type
Interventional
Enrollment
90
Allocation
Non-randomized
Ages
21 Years to 60 Years
Sex
All
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Study summary

This study aims to examine patient outcomes following risk stratification for low back pain in Family Medicine combined with either matched physical therapy (PT - i.e., stratified-specific PT) treatments or current treatment in primary care across The University of Vermont Health Network.

Read the detailed description

The University of Vermont Health Network is a five hospital network that serves primarily a rural population of approximately 1 million people in Vermont and upstate New York. The primary aim of this prospective, longitudinal, pragmatic, non-randomized clustered, non-blinded, controlled trial is to examine whether PT treatment stratified to match the patient's risk factors based on the STarT Back Tool is more effective than the current treatment in primary care for non-specific low back pain (LBP) in improving short- (6 months) and long-term (12-month) patient outcomes (disability).

To do the risk stratification, investigators will use the STarT Back Tool which is designed for primary care settings and is validated for non-specific LBP (acute flare-ups or chronic pain). The tool is designed to identify the prognostic risk (low, medium, high) for progression to chronic LBP. In addition, the tool assists clinicians in decision making to ensure that low risk patients are not over treated or medicalized, that 'at risk' patients get access to the right provider early on and that enhanced care is given for complex cases. Thus, the tool assists in matching the 'right patient to the right treatment' at the 'right time' which is critical given the high prevalence and cost of LBP.

Patients with a primary diagnosis of LBP (acute flare-up or chronic) who are seen in any of the six Family Medicine sites will complete the STarT Back Tool and the Modified Low Back Pain Disability Questionnaire (mODI). With the non-randomized, cluster design, three of the Family Medicine sites are identified as "Participating Sites" and three are identified as "Comparator Sites." Patients with low back pain from "Participating Sites" who are stratified as medium- or high-risk patients will be referred to physical therapy (PT) for a matched (i.e., stratified-specific treatment). Those patients who are identified as low-risk will be retained in Family Medicine for management using advice, reassurance, patient education, NSAIDs (no imaging or specialist referral is encouraged). Patients with low back pain from "Comparator Sites" will be managed according to current care practices in Family Medicine. Using the mODI, the investigators will compare the two study arms at short- (6 months) and long-term points (12 months).

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Conditions studied

  • Low Back Pain

Keywords

  • stratified care
  • psychologically informed practice
  • matched care
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In context

Back Pain

2,373 studies on the registry are indexed under Back Pain; 284 are open to participants now.

This study's enrollment of 90 is above the median of 60 across 1,941 interventional studies indexed under Back Pain.

Browse Back Pain studies →

Lead sponsor

University of Vermont Medical Center is the lead sponsor of 41 studies on the registry; 19 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
21 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. diagnosis of acute, chronic or non-specific LBP,
  2. between 21 - 60 years of age,
  3. able to stand and walk without assistance,
  4. able to understand and read English,
  5. able to understand and sign a consent form.

Exclusion criteria

Exclusion Criteria:

  1. active serious spinal complications such as tumor or infection,
  2. active treatment for metastatic or bone cancer of the spine,
  3. pregnancy or less than 6 months post-partum or less than 6 months post weaning.
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
90 participants (actual)

Study arms

  • Experimental
    Stratified Care

    In three "Participating Sites" from Family Medicine sites, the Keele STarT Back Screening Tool will be administered to patients with acute and chronic low back pain and based on patients' responses, patients will be stratified into one of three risk groups: low, medium or high-risk. Patients in the medium- and high-risk groups will be referred to physical therapy for a matched physical therapy (PT) intervention based on the risk strata. Patients in the low-risk group will be managed in Family Medicine with an intervention that includes advice, reassurance, patient education, and NSAIDs (with no referral for imaging or specialist care).

    Other: Matched Physical Therapy Intervention

  • Active comparator
    Current Care

    In three "Comparator Sites" from Family Medicine, providers will give the current care at The University of Vermont Medical Center for patients with acute and chronic low back pain.

    Other: Current Care in Family Medicine

Interventions

  • OtherMatched Physical Therapy Intervention

    Patients who are medium-risk will receive up to 6-8 physical therapy (PT) visits over a 3 month period that is guided by published evidence based practice guidelines. The PT treatment will be tailored to the physical findings and specific patient needs, and appropriate exercises, spinal mobilization/manipulation, strengthening/stretching as well as a home program will be given to improve patient pain and function and reduce disability. Patients who are high-risk will receive the evidence based PT treatment as deemed necessary. In addition, the PT treatment will incorporate principles of psychologically informed practice to address psychosocial barriers (e.g., fear avoidance, anxiety, etc) that may be impeding disability reduction. This may include instruction on chronic pain rehabilitation techniques such as the use of: pacing in order to maintain or increase activity; graded activity principles in order to increase function; and pain education and understanding responses to pain.

  • OtherCurrent Care in Family Medicine

    Patient education, medication management

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What researchers measure

Primary outcomes

  1. Modified Low Back Pain Disability Questionnaire

    Low back pain disability measure

    Time frame: 6 months

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Study locations

1 site
  • University of Vermont Medical Center
    Burlington, Vermont 05401, United States
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 7, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03065894
Lead sponsor
University of Vermont Medical Center
Responsible party
Sharon Henry (Therapy Research Educator, University of Vermont Medical Center) — Principal investigator
First posted
Feb 28, 2017
Start date
Mar 29, 2017
Primary completion
Aug 31, 2018
Completion
Aug 31, 2018
Last update
Sep 7, 2018

Study contacts

Sharon M Henry, PT, PhD
principal investigator · The University of Vermont Medical Center

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Sep 2018. You cannot join it, but the record below documents what was studied.

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