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Clinical Trials/NCT06537219
NCT06537219
Recruiting
Not Applicable

Thoracolumbar Fascia Stiffness and Pain Parameters

Atılım University1 site in 1 country50 target enrollmentJuly 15, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pain
Sponsor
Atılım University
Enrollment
50
Locations
1
Primary Endpoint
Numerical Pain Scale(NMS
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

This study aims to investigate the biomechanical parameters of thoracolumbar fascia (TLF) and pain-related properties including pain intensity, pressure pain threshold (ppt) and pain sensitivity in young adults with non-specific chronic low back pain (LBP), both those experiencing chronic low back pain (LBP) and without LBP.

Detailed Description

Non-specific low back pain has become a serious public health problem in latest years. The prevalence of low back pain is reported to be 84% in lifetime (1). Recently, an increasing number of studies have reported that fascia, due to its rich nociceptive innervations, may play a role in chronic pain, especially in some non-specific low back pain conditions . This study will conducted with a total of 50 participant, including those with chronic lower back pain in the experimental group and the control group. Both groups underwent assessments related to pain properties. Specifically, the Numerical Pain Scale(NMS) will be used to assess subjective pain intensity(4), the Digital Algometer for assessing pressure pain treshold(5), the Pain Sensitivity Scale(PSS) pain sensitivity(6) and the Myotonometer MyotonPRO biomechanical parameters, including stiffness(s), elasticity(d) and tonus (f) of the TFL at the level of Lumbal 1,3 vertebrae(L1,L3) and under 12th costa (7-10). SPSS 23.0 will be used for statistical analysis. p\<0.05 is considered statistically significant.

Registry
clinicaltrials.gov
Start Date
July 15, 2024
End Date
September 15, 2024
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
Atılım University
Responsible Party
Principal Investigator
Principal Investigator

NAİME ULUG

Assistant Professor

Atılım University

Eligibility Criteria

Inclusion Criteria

  • chronic back pain participants more than 3 months

Exclusion Criteria

  • Those with orthopaedic, neurological and systemic diseases will be excluded from the study.

Outcomes

Primary Outcomes

Numerical Pain Scale(NMS

Time Frame: 1 month

pain assessment

the Pain Sensitivity Scale(PSS)

Time Frame: month

Pain sensitivity assessment

Fascia stiffness

Time Frame: 1month

thoracolumbar fascia stiffness assessment

Study Sites (1)

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