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Changes in Thoracolumbar Fascia Stiffness and Pain Parameters in Young Patients With Chronic Low Back Pain

A

Atılım University

Status

Enrolling

Conditions

Fascia
Back Pain
Pain

Treatments

Other: Assessment

Study type

Observational

Funder types

Other

Identifiers

NCT06537219
E-59394181-604.01-79246

Details and patient eligibility

About

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.

Full 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.

Enrollment

50 estimated patients

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

50 participants in 2 patient groups

back pain group
Description:
participants with chronic back pain( pain duration at least 3 months) aged between 18 and 50 years , male and female participanst will be included in the study. Those with orthopaedic, neurological and systemic diseases will be excluded from the study.
Treatment:
Other: Assessment
control group
Description:
healty male and female participants aged between 18 and 50 years
Treatment:
Other: Assessment

Trial contacts and locations

1

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Central trial contact

Süleyman Korkusuz, PT,PhD; Naime Uluğ, PT,PhD

Data sourced from clinicaltrials.gov

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