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Completed

NCT Number: NCT03722394

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

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).

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Nevada Las Vegas

Las Vegas, Nevada, 89178, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

pain neuroscience education

Behavioral

15 minute verbal one-on-one education session

Primary outcomes

  1. NPRS - LBP

    Time frame: Immediate change from baseline after assigned intervention

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

  2. NPRS - Leg pain

    Time frame: Immediate change from baseline after assigned intervention

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

Secondary outcomes

  1. Active trunk flexion

    Time frame: Immediate change from baseline in centimeters after assigned intervention

    Active trunk flexion measured in centimeters from fingertips to floor

  2. Passive Straight Leg Raise

    Time frame: Immediate change from baseline in angular degrees after assigned intervention

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

Sponsors and collaborators

Lead sponsor

University of Nevada, Las Vegas

Other

Collaborators

  • St. Ambrose University

Registry information

Official study title

Pain Neuroscience Education for Acute and Sub-Acute Low Back Pain: An Exploratory Case Series

Important dates

Study start
2018
Primary completion
2018
Study completion
2018
First posted
Oct 26, 2018
Registry last updated
Oct 26, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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