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CompletedNCT07441213Updated Feb 27, 2026

Viscous Elastic Properties of Superficial Back Muscles in Individuals With Hyperkyphosis

An observational study in Hyperkyphosis and Viscoelasticity, sponsored by Sanko University. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-02-27.

Sponsored by Sanko University · Observational

Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
88
Ages
18 Years to 65 Years
Sex
All
01

Study summary

Thoracic hyperkyphosis is a common spinal deformity that may alter the biomechanical and viscoelastic properties of trunk muscles. This comparative study aims to investigate differences in the mechanical properties of selected back and chest muscles between individuals with hyperkyphosis and healthy controls.

A total of 88 participants will be categorized based on thoracic kyphosis angle (≥50° hyperkyphosis; \<50° control). The kyphosis angle will be measured using a flexible ruler method. Muscle tone, stiffness, elasticity, and relaxation properties of the trapezius, erector spinae, and pectoralis major muscles will be assessed using a handheld myotonometer. Spinal appearance perception will be evaluated using a kyphosis-specific questionnaire.

The study is designed to examine whether differences exist in muscle mechanical properties and whether kyphosis severity is associated with asymmetry in viscoelastic muscle characteristics.

Read the detailed description

Thoracic hyperkyphosis is a frequently observed spinal deformity characterized by an excessive posterior curvature of the thoracic spine. Increased kyphotic posture is associated with altered biomechanical loading, postural imbalance, reduced functional capacity, and changes in muscle performance. Although previous studies have largely focused on muscle tightness and postural alignment, limited evidence exists regarding the viscoelastic mechanical properties of trunk muscles in individuals with hyperkyphosis.

The mechanical behavior of skeletal muscle-including tone, stiffness, elasticity, and relaxation properties-reflects neuromuscular adaptation and tissue integrity. Changes in spinal curvature may lead to asymmetrical loading patterns between the anterior and posterior trunk muscles, potentially resulting in measurable differences in muscle viscoelastic characteristics. Understanding these adaptations may provide insight into rehabilitation strategies targeting both anterior and posterior muscle groups.

This comparative study is designed to evaluate and compare the viscoelastic properties of selected trunk muscles in individuals with thoracic hyperkyphosis and healthy controls. Participants are classified into two groups based on thoracic kyphosis angle measurements: individuals with a kyphosis angle of 50 degrees or greater are assigned to the hyperkyphosis group, while those with an angle below 50 degrees form the control group. The thoracic kyphosis angle is assessed using a flexible ruler method.

Muscle mechanical properties of the upper trapezius, erector spinae, and pectoralis major muscles are assessed bilaterally using a handheld myotonometer device. Parameters recorded include muscle tone (frequency), stiffness, elasticity, and relaxation time. In addition, participants' perception of spinal appearance is evaluated using a kyphosis-specific spinal appearance questionnaire.

The primary objective of the study is to determine whether individuals with hyperkyphosis demonstrate altered or asymmetric viscoelastic muscle properties compared to healthy individuals. A secondary objective is to explore the relationship between kyphosis severity and muscle mechanical characteristics.

The results of this study are expected to provide further information regarding muscular adaptations associated with thoracic hyperkyphosis and to support the development of comprehensive rehabilitation approaches targeting anterior chest and posterior trunk musculature.

02

Conditions studied

  • Hyperkyphosis
  • Viscoelasticity

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Keywords

  • viscoelasticity
  • hyperkyphosis
03

In context

Kyphosis

132 studies on the registry are indexed under Kyphosis; 31 are open to participants now.

This study's enrollment of 88 is above the median of 62 across 45 observational studies indexed under Kyphosis.

Browse Kyphosis studies →

Lead sponsor

Sanko University is the lead sponsor of 52 studies on the registry; 11 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

individual with hyperkyphosis

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Individuals with a kyphosis angle of ≥50° and ≤50º were evaluated for eligibility. The inclusion criteria were: having a hyperkyphosis degree of ≥50°, a physiologic curve of the thoracic degree of ≤50º, and voluntarily participating in the study.

Exclusion criteria

Exclusion Criteria:

  • individuals with scoliosis, Scheuermann's kyphosis, and other congenital spinal problems.
05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
88 participants (actual)
Patient registry
No

Groups and cohorts

  • individuals with hyperkyphosis

    thoracic kyphosis angles of ≥ 50◦ hyperkyphosis

06

What researchers measure

Primary outcomes

  1. Flexible Ruler

    Flexible Ruler The flexible ruler method is a reliable method used to measure cervical, thoracic, and lumbar spine curvature. The measurement is taken using a 40 cm long flexible ruler while standing with arms relaxed at the sides, head upright, and eyes looking straight ahead. The C2 and C7 vertebrae are palpated and marked using removable adhesive skin markers. The flexible ruler is then placed over the cervical lordosis between these two points, and markers indicating the location of the C2 and C7 spinous processes are placed on it. The flexible ruler is placed on millimeter paper, and the resulting curve is reflected. A vertical angle is drawn from the peak of the curve to the baseline, and the cervical lordosis deviation angle is determined using an angle-to-angle connection

    Time frame: 3 months

  2. MyotonPro- Tone

    Viscoelastic Properties of Muscles The MyotonPro® device can determine the stiffness, tone, and elasticity properties of muscles. This previously calibrated device creates a mechanical stimulus that induces the damped natural oscillations of the tissues using a 3 mm diameter probe placed perpendicular to the muscle with a non-invasive handheld feature. The resulting oscillations are recorded by an accelerometer. MyotonPro® is a valid and reliable method for determining muscle tone.

    Time frame: 3 months

  3. Kyphosis-Specific Spine Appearance Questionnaire

    Kyphosis-Specific Spine Appearance Questionnaire The Kyphosis-Specific Spine Appearance Questionnaire consisted of 10 items on a Likert scale (1 to 5) regarding patients' perceptions of appearance; higher scores indicated worsening deformity and increased concern about kyphosis-specific appearance. The first item is based on drawings showing varying degrees of severity of hyperkyphosis deformity in the sagittal plane. Questions two through ten are based on textual questions that rate concerns about other aspects of spinal deformity appearance. The total score of the questionnaire is calculated as the average of the ten responses

    Time frame: 3 months

  4. myoton pro- stiffness

    Viscoelastic Properties of Muscles The MyotonPro® device can determine the stiffness, tone, and elasticity properties of muscles. This previously calibrated device creates a mechanical stimulus that induces the damped natural oscillations of the tissues using a 3 mm diameter probe placed perpendicular to the muscle with a non-invasive handheld feature. The resulting oscillations are recorded by an accelerometer. MyotonPro® is a valid and reliable method for determining muscle stiffness.

    Time frame: 3 months

  5. myoton pro - elasticity

    Viscoelastic Properties of Muscles The MyotonPro® device can determine the stiffness, tone, and elasticity properties of muscles. This previously calibrated device creates a mechanical stimulus that induces the damped natural oscillations of the tissues using a 3 mm diameter probe placed perpendicular to the muscle with a non-invasive handheld feature. The resulting oscillations are recorded by an accelerometer. MyotonPro® is a valid and reliable method for determining muscle elasticity.

    Time frame: 3 months

07

Study locations

1 site
  • Sanko Unıversıty
    Gaziantep, Gaziantep 27090, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Nov 2025 to primary completion in Dec 2025, 1 month.

How these figures are worked out, and which studies are left out of them.

Registered
Feb 18, 2026
First posted
Feb 27, 2026
StartActual
Nov 1, 2025
Primary completionActual
Dec 15, 2025
CompletionActual
Jan 15, 2026
Last update
Feb 27, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Feb 27, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07441213
Lead sponsor
Sanko University
Responsible party
Hakan Polat (dırector, Sanko University) — Principal investigator
First posted
Feb 27, 2026
Start date
Nov 1, 2025
Primary completion
Dec 15, 2025
Completion
Jan 15, 2026
Last update
Feb 27, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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