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Pain Neuroscience Education for Acute and Sub-Acute Low Back Pain

Not Applicable
Completed
Conditions
Low Back Pain
Pain, Back
Pain, Chronic
Interventions
Behavioral: Pain Neuroscience Education
Registration Number
NCT03722394
Lead Sponsor
University of Nevada, Las Vegas
Brief Summary

To determine if Pain Neuroscience Education (PNE) would result in positive clinical changes in patients presenting with acute or sub-acute low back pain (LBP).

Detailed Description

Background: Pain neuroscience education (PNE) has shown efficacy in treating chronic pain. Clinicians may believe PNE is not suitable for acute and sub-acute pain. Subgroupings of low back pain (LBP) imply some patients with LBP may respond favorably to PNE.

Objective: To determine if PNE would result in positive clinical changes in patients presenting with acute or sub-acute LBP.

Methods: Eighty consecutive patients with LBP \< 3 months were enrolled in the study. Patients completed a demographics questionnaire, leg and LBP rating (Numeric Pain Rating Scale - NPRS), disability (Oswestry Disability Index), fear-avoidance (Fear-Avoidance Beliefs Questionnaire), pain catastrophization (Pain Catastrophization Scale), central sensitization (Central Sensitization Inventory), pain knowledge (Revised Neurophysiology of Pain Questionnaire), risk assessment (Keele STarT Back Screening Tool), active trunk flexion and straight leg raise (SLR). Patients received a 15-minute verbal, one-on-one PNE session, followed by repeat measurement of LBP and leg pain (NPRS), trunk flexion and SLR.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
80
Inclusion Criteria
  • a complaint of LBP with or without leg pain less than 3 months, and
  • a willingness to participate
Exclusion Criteria
  • a) were under age 18 (minor);
  • b) had undergone lumbar surgery;
  • c) could not read or understand the English language;
  • d) presented with any cognitive deficits rendering them unsuitable for PNE (i.e., stroke, traumatic brain injury, etc.),
  • e) declined to participate or
  • f) presented with a medical etiology (red flag) associated with their LBP.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Pain Neuroscience EducationPain Neuroscience EducationSubjects received a 15-minute verbal, one-on-one Pain Neuroscience Education (PNE) session
Primary Outcome Measures
NameTimeMethod
NPRS - LBPImmediate change from baseline after assigned intervention

Numeric Pain Rating Scale for Low Back Pain (Range 0 = no pain to 11 = maximum pain)

NPRS - Leg painImmediate change from baseline after assigned intervention

Numeric Pain Rating Scale for leg pain (Range 0 = no pain to 11 = maximum pain)

Secondary Outcome Measures
NameTimeMethod
Passive Straight Leg RaiseImmediate change from baseline in angular degrees after assigned intervention

Range of hip flexion angle during passive straight leg raise test measured in degrees

Active trunk flexionImmediate change from baseline in centimeters after assigned intervention

Active trunk flexion measured in centimeters from fingertips to floor

Trial Locations

Locations (1)

University of Nevada Las Vegas

🇺🇸

Las Vegas, Nevada, United States

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