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Clinical Trials/NCT03901365
NCT03901365
Completed
Not Applicable

The Effect of Neuroplastic Pain Education on Quality of Life in Patients with Chronic Low Back Pain Who Treated Via Manual Therapy: a Single Blind Randomized Controlled Study

Kutahya Health Sciences University1 site in 1 country35 target enrollmentApril 1, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Low Back Pain
Sponsor
Kutahya Health Sciences University
Enrollment
35
Locations
1
Primary Endpoint
Quality of Life (QOL): Turkish Short form-36 (SF-36) questionnaire
Status
Completed
Last Updated
last year

Overview

Brief Summary

Manual therapy are among the therapeutic approaches frequently used in chronic low back pain (CLBP). Although most clinicians conduct patient education according biomedical model of pain, a relatively new approach which is referred to as neuroscience pain education (NPE) is promising in patients with CLBP. Therefore the aim of this study was to investigate whether NPE in patients with CLBP who treated via manual therapy technique will produce different outcomes in terms of pain severity and QoL compared to traditional patient education.

Registry
clinicaltrials.gov
Start Date
April 1, 2018
End Date
November 30, 2018
Last Updated
last year
Study Type
Interventional
Study Design
Factorial
Sex
All

Investigators

Sponsor
Kutahya Health Sciences University
Responsible Party
Principal Investigator
Principal Investigator

Ismail Saracoglu

Principal Investigator,

Kutahya Health Sciences University

Eligibility Criteria

Inclusion Criteria

  • Volunteered to participate in the study.
  • Patients with 18-65 years
  • Had low back pain for at least 6 months,
  • Reported pain severity of 5 or greater according to the numeric pain rating scale

Exclusion Criteria

  • Previous spine or lower extremity surgery
  • Severe osteoporosis
  • Spondyloarthropathy
  • Spondylolisthesis
  • Lumbar stenosis
  • Lumbar fractures
  • Malign tumor

Outcomes

Primary Outcomes

Quality of Life (QOL): Turkish Short form-36 (SF-36) questionnaire

Time Frame: Change from Baseline SF-36 at 4th weeks.

All patients additionally completed Turkish Short form-36 (SF-36) questionnaire, 36-item generic self-administered instrument that consists of eight subscales relating to various aspects of the QoL: physical functioning, physical role, bodily pain, general health, vitality, social functioning, emotional role and mental health. The eight subscales are scored from 0 to 100, with higher scores indicating better health status

Secondary Outcomes

  • Numeric Pain Rating Scale (NPRS)(Change from Baseline NPRS at 4th weeks.)

Study Sites (1)

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