ClinicalTrials.Veeva

Menu

Pain Neuroscience Education and Exercise for Chronic Nonspecific Low Back Pain

H

Hacettepe University

Status

Active, not recruiting

Conditions

Chronic Non-specific Low Back Pain

Treatments

Other: Motor Control Exercises
Other: Pain Neuroscience Education

Study type

Interventional

Funder types

Other

Identifiers

NCT07202533
Hacettepe-FTR-AŞ-01

Details and patient eligibility

About

This study aims to evaluate the effects of adding Pain Neuroscience Education (PNE) to motor control exercises in individuals with chronic non-specific low back pain (CNSLBP) who also present with central sensitization. The study focuses on changes in pain intensity, pain-related factors, trunk muscle activation, gait, functionality, kinesiophobia, and quality of life.

Full description

This randomized controlled study aims to investigate the effects of combining PNE with motor control exercises in individuals with CNSLBP who demonstrate central sensitization (≥28 points on the Central Sensitization Inventory). Participants are randomly assigned into two groups: the intervention group (motor control exercises + PNE) and the control group (motor control exercises only). Both groups participate in motor control exercises twice a week for 8 weeks, under the supervision of a physiotherapist. The intervention group additionally receives six PNE sessions once per week for six weeks. PNE sessions are delivered by a certified physiotherapist using interactive presentations and question-answer discussions.

Assessments are performed pre- and post-intervention using the following tools:

  • Central Sensitization Inventory (CSI) to determine the presence and severity of central sensitization.
  • Numeric Pain Rating Scale (NPRS) for pain intensity.
  • Revised Neurophysiology of Pain Questionnaire (rNPQ) for pain knowledge.
  • Pain Catastrophizing Scale (PCS) for catastrophic thinking.
  • Pressure Pain Threshold (PPT) using a digital algometer.
  • Electromyographic (EMG) evaluation of trunk and lower extremity muscles using surface electrodes.
  • Spatiotemporal gait analysis using OptoGait and Ultium Insole systems.
  • Tampa Scale for Kinesiophobia (TSK) for fear of movement.
  • Roland-Morris Disability Questionnaire (RMDQ) for disability level.
  • Nottingham Health Profile (NHP) for quality of life.

Data will be analyzed using SPSS version 27. Normality of distribution will be tested with the Shapiro-Wilk test. Depending on the distribution, either parametric (paired t-test, independent t-test) or non-parametric tests (Wilcoxon signed-rank, Mann-Whitney U) will be applied. Pearson or Spearman correlation analyses will be used where appropriate.

Enrollment

20 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Volunteers who agree to participate in the study
  • Having a history of non-specific low back pain lasting at least 3 months
  • Having a pain intensity score of 3 or higher on the Numerical Pain Rating Scale (NPRS) within the last week
  • Scoring ≥28 on the Turkish version of the Central Sensitization Inventory.

Exclusion criteria

  • Individuals with radicular symptoms or cauda equina syndrome
  • Severe osteoporosis
  • Spondyloarthropathy
  • Spondylolisthesis
  • Lumbar spinal stenosis
  • Lumbar fractures
  • Malignant tumors
  • Severe comorbidities (neurological, neuromuscular, cardiac, or psychiatric disorders)
  • Individuals who have undergone spinal surgery
  • Individuals who are familiar with motor control exercises or who have previously received pain neuroscience education

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

20 participants in 2 patient groups

Motor Control Exercises
Active Comparator group
Description:
This group will receive motor control exercises only.
Treatment:
Other: Motor Control Exercises
Other: Motor Control Exercises
Motor Control Exercises + Pain Neuroscience Education
Experimental group
Description:
This group will receive the same motor control exercise program as the control group, plus a 6-week PNE program delivered once per week. The PNE program consists of 6 weekly sessions, delivered via slide presentations and interactive discussions, covering topics such as nociception, central sensitization, neuroplasticity, and pain coping strategies. Sessions are delivered by a certified physiotherapist.
Treatment:
Other: Motor Control Exercises
Other: Pain Neuroscience Education
Other: Motor Control Exercises

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems