Mode
Text Size
Log in / Sign up
N/A N=38 Randomized Single-blind Treatment

Effectiveness of Core Stabilization Exercise in Patients With Subacute Non-Specific Low Back Pain

Low Back Pain

Enrolled (actual)
38
Serious AEs
0.0%
Results posted
Oct 2016
Primary outcome: Primary: Change From Baseline in Pain on 11- Point Numerical Rating Scale at Week 7 — 1.32; 3.63 units on a scale — p=<0.001

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Core stabilization exercise (Other); Conventional treatment (Other)
Age
Adult · 18+ yrs
Sex
All
Sponsor
Khon Kaen University
Primary completion
Jun 2016

Outcome Measures

OutcomeResultp-value
PRIMARY
Change From Baseline in Pain on 11- Point Numerical Rating Scale at Week 7
1.32; 3.63 <0.001 sig
SECONDARY
Change From Baseline in Functional Disability on Roland-Morris Disability Questionnaire at Week 7
1.53; 4.89 0.009 sig
SECONDARY
Change From Baseline in Back Range of Motion (Flexion) on Modified-modified Schober's Test at Week 7
5.32; 4.32 0.013 sig
SECONDARY
Change From Baseline in Repositioning Error on Repositioning Test at Week 7
0.43; 0.67 0.012 sig

Summary

The purpose of this study is to examines the effectiveness of Core stabilization exercise on pain intensity at rest, functional disability, lumbar movement and ability to perform repositioning tasks (joint position sense) in patients with subacute non-specific low back pain.

Eligibility Criteria

Inclusion Criteria

  • Onset of back pain within 6 -12 weeks participants had no history of back pain for a period of 6 months prior to the current episode.
  • Pain intensity measure by a numerical rating scale (0-10 NRS) and a score of pain at least 3 out of 10.
  • Never receive the treatment by core stabilization exercise (CSE) during 3 months before participate in this study.

Exclusion Criteria

  • Pregnancy
  • Onset of serious spinal pathology: spinal fracture, spinal tumor or spinal infection.
  • Cauda equina syndrome.
  • Presented at least 2 out of 3 signs of neurological deficit
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02645760). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search