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KyphosisTK-DNS-TSNCT07255794

DNS vs Thoracic Stabilization Exercises in Thoracic Kyphosis

A study testing Dynamic Neuromuscular Stabilization Exercises and Thoracic Stabilization Exercise in people with Kyphosis, run by Esra BECENI at 1 site in Turkey (Türkiye).

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

This randomized controlled trial aims to compare the effects of Dynamic Neuromuscular Stabilization (DNS) exercises and thoracic stabilization exercises on thoracic erector spinae muscle strength, thoracic kyphosis angle, pain and trunk stabilization in individuals with thoracic kyphosis. Read more about this study

Who is it for?
Ages 18 to 40 years
Conditions the study is for
Kyphosis
What is being tested?
Dynamic Neuromuscular Stabilization Exercises and Thoracic Stabilization Exercise
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
1 siteTurkey (Türkiye)
Study dates
1 Dec 2025to 15 Feb 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 40 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Age between 18 and 40 years.
  • Presence of thoracic kyphosis based on clinical and flexible ruler assessment.
  • Able to perform exercise-based interventions.
  • Voluntarily agrees to participate and signs the informed consent form.
  • No neurological, systemic, cardiac or orthopedic condition that would prevent safe participation in the exercise program.

Who cannot join

  • Age outside the range of 18-40 years.
  • Pregnancy.
  • Malignancy.
  • History of spinal surgery within the last year.
  • Currently performing spinal or intensive core stabilization exercises.
  • Visual, auditory or cognitive impairment that would interfere with cooperation during the intervention.
  • Contraindications to exercise participation.
  • Non-adherence to the exercise program (not performing exercises for three consecutive days).

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Esra Beceni, Lecturer contact

+905387358097

esra.beceni@mudanya.edu.tr

Server Erdoğmuş Gülcan, PhD Students contact

+905397829714

server.erdogmus@mudanya.edu.tr

Turkey (Türkiye)1 site
  • Mudanya University

    Bursa, 16940

Other trials in Turkey (Türkiye)

About this study

Official title: Comparison of the Effects of Dynamic Neuromuscular Stabilization and Thoracic Stabilization Exercises on Thoracic Erector Spinae Muscle Strength Using EMG Biofeedback in Individuals With Kyphosis

This randomized controlled trial aims to compare the effects of Dynamic Neuromuscular Stabilization (DNS) exercises and thoracic stabilization exercises on thoracic erector spinae muscle strength, thoracic kyphosis angle, pain and trunk stabilization in individuals with thoracic kyphosis. Thirty participants aged 18-40 years with thoracic kyphosis will be randomly allocated to a DNS exercise group or a thoracic stabilization exercise group. Surface EMG biofeedback will be used to assess thoracic erector spinae muscle activation, while pain, thoracic kyphosis angle and trunk endurance will be evaluated using validated clinical tests. The interventions will be applied for 6 weeks, and outcomes will be assessed before and after the intervention period.

Read the detailed description

Thoracic kyphosis is a frequently observed postural deviation that affects the sagittal alignment of the spine and may lead to alterations in muscular balance, impaired trunk stability, and increased biomechanical stress on the vertebral column. Postural thoracic kyphosis typically results from prolonged sedentary behaviors-such as extended computer and smartphone use-and habitual forward-flexed postures adopted during work or daily activities. Over time, inadequate thoracic extension, weakness of the thoracic erector spinae musculature, and compensatory recruitment of accessory trunk muscles may further contribute to the progression of the deformity. Although postural kyphosis is considered flexible and reversible in early stages, insufficient management may allow gradual transition toward more structural changes.

Conservative physiotherapy interventions represent the primary approach to managing postural thoracic kyphosis. These interventions traditionally include thoracic mobility exercises, strengthening of the spinal extensors, scapular stabilization strategies, and postural retraining. In recent years, neuromuscular re-education methods and biofeedback-supported interventions have become increasingly prominent, reflecting a shift toward approaches that emphasize sensorimotor control and integration of respiratory-postural synergy.

Dynamic Neuromuscular Stabilization (DNS) is a rehabilitation method grounded in developmental kinesiology principles. DNS aims to restore optimal joint stabilization and postural alignment through coordinated activation of the diaphragm, deep spinal stabilizers, and global trunk musculature. By replicating developmental postures, DNS seeks to reintegrate diaphragmatic breathing patterns and promote central stabilization strategies that influence thoracic alignment and motor control.

Thoracic stabilization exercises represent another commonly applied approach and typically include targeted thoracic extension, scapular retraction, and segmental mobilization techniques. These exercises aim to improve local muscle function of the thoracic erector spinae, enhance thoracic mobility, and promote more efficient load transfer across the spine. While both DNS and thoracic stabilization approaches have theoretical and clinical justification, direct comparative evidence regarding their short-term effects on neuromuscular activation and postural correction in adults with thoracic kyphosis remains limited.

This single-center randomized controlled trial will be conducted at Mudanya University and will include 30 adults aged 18 to 40 years with postural thoracic kyphosis confirmed through flexible ruler assessment. Participants will be randomly assigned in a 1:1 ratio to either a Dynamic Neuromuscular Stabilization intervention group or a Thoracic Stabilization Exercise group. Both intervention programs will extend over a 6-week period and will include two supervised sessions per week, complemented by home-based exercises performed twice daily. To ensure adherence, each participant will maintain an exercise diary, and individuals who fail to perform the prescribed exercises for three consecutive days will be withdrawn from the study in accordance with predefined adherence criteria.

Outcome measures will be collected at baseline and after the 6-week intervention. Surface electromyography (EMG) biofeedback will be used to assess thoracic erector spinae muscle activity. Pain intensity will be evaluated using the Visual Analog Scale (VAS). Trunk endurance and stabilization capacity will be measured using standardized plank tests and the Biering-Sørensen back endurance test. Thoracic curvature will be quantified using a flexible ruler, from which a kyphosis index will be calculated. Additional data-such as demographic characteristics, body mass index, and relevant medical history-will be recorded to contextualize findings and ensure appropriate characterization of the study population.

The primary aim of this trial is to compare the effects of DNS and thoracic stabilization exercises on thoracic erector spinae muscle activation measured via EMG. Secondary objectives include comparing the influence of both interventions on thoracic kyphosis angle, pain intensity, and trunk stabilization performance. The study is designed to provide a detailed evaluation of two physiotherapy approaches grounded in distinct theoretical frameworks, thereby offering insight into their mechanisms and potential applicability for individuals presenting with postural thoracic kyphosis. Findings will be reported separately in the Results section once data collection and analysis are completed. The present description outlines the scientific rationale and methodological approach without including results or interpretations.

Conditions
Kyphosis
Being tested
Dynamic Neuromuscular Stabilization Exercises, Thoracic Stabilization Exercise
Keywords
dynamic neuromuscular stabilization(DNS), electromyography, thoracic stabilization exercises
Medical subject headings
Kyphosis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Dynamic Neuromuscular Stabilization ExercisesBehavioural

    Participants in the DNS group will perform Dynamic Neuromuscular Stabilization exercises based on developmental kinesiology. The program includes prone (4.5-month position), modified prone over a Swiss ball, quadruped (9-month position) and prone exercises on a Swiss ball with bilateral hand support. All exercises emphasize proper spinal alignment, diaphragmatic breathing and coordinated activation of the deep stabilizing muscles. Participants will complete two supervised sessions per week and perform home exercises twice daily (10 repetitions per exercise) for 6 weeks. An exercise diary will be used to monitor adherence.

  • Thoracic Stabilization ExerciseBehavioural

    Participants in the thoracic stabilization group will perform a structured thoracic and scapular stabilization program including foam roller thoracic extension in supine, prone thoracic extension, child's pose with thoracic extension and scapular retraction exercises. The exercises are designed to improve thoracic mobility, strengthen the thoracic extensors and enhance postural alignment. Participants will complete two supervised sessions per week and perform home exercises twice daily (10 repetitions per exercise) for 6 weeks. Exercise adherence will be tracked with an exercise diary, and participants who miss the program for three consecutive days will be withdrawn from the study.

Study groups in NCT07255794
Study groupRoleWhat they receive
Dynamic Neuromuscular Stabilization (DNS) Group (DNSG)ExperimentalNot described
Receives: Behavioral: Dynamic Neuromuscular Stabilization Exercises
Thoracic Stabilization Exercise Group (TSG)ExperimentalNot described
Receives: Behavioral: Thoracic Stabilization Exercise

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Thoracic Kyphosis Index (Flexible Ruler Measurement)

    Thoracic kyphosis will be measured using a flexible ruler placed from C7 to T12 in standing posture. The curve will be transferred to paper and the kyphosis index will be calculated using the formula (H/U) × 100, where H is the height and U is the length of the curve. Higher scores indicate greater kyphosis.

    Analysis Metric:

    Change from baseline to Week 6 in kyphosis index.

    Measured: Baseline and Week 6

Secondary outcomes (5)
  1. Thoracic Erector Spinae Muscle Activity (Surface EMG, µV)

    Thoracic erector spinae muscle activity will be evaluated using surface EMG biofeedback. Surface electrodes will be placed along the thoracic erector spinae musculature. Participants will perform standardized isometric contractions, and mean microvolt (µV) amplitudes will be recorded at baseline and after 6 weeks of intervention.

    Analysis Metric:

    Change from baseline to Week 6 in mean EMG amplitude (µV).

    Measured: Baseline and Week 6

  2. Pain Intensity - Visual Analog Scale (VAS)

    Pain intensity will be assessed using a 10-cm Visual Analog Scale, where 0 indicates no pain and 10 indicates worst imaginable pain. Participants will rate their pain at baseline and after 6 weeks.

    Analysis Metric:

    Change from baseline to Week 6 in VAS score.

    Measured: Baseline and Week 6

  3. Plank Test (Core Endurance, seconds)

    Core muscle endurance will be assessed using the prone plank test. Participants will maintain a standardized prone plank position supported on forearms and toes for as long as possible. Time to fatigue (seconds) will be recorded.

    Analysis Metric:

    Change from baseline to Week 6 in plank hold time (seconds).

    Measured: Baseline and Week 6

  4. Lateral Plank Test (Oblique Endurance, seconds)

    Lateral plank tests will be used to assess lateral trunk endurance. Participants will support their body on one elbow and the side of the foot, maintaining a straight alignment. Time to fatigue will be recorded separately for both sides.

    Analysis Metric:

    Change from baseline to Week 6 in side plank hold time (seconds).

    Measured: Baseline and Week 6

  5. Sorensen Back Extensor Endurance Test (seconds)

    Back extensor endurance will be evaluated using the Biering-Sørensen test. With the lower body fixed to the examination table at the level of the iliac crests, participants will maintain the upper body in a horizontal position unsupported as long as possible. Time to fatigue (seconds) will be recorded.

    Analysis Metric:

    Change from baseline to Week 6 in endurance time (seconds).

    Measured: Baseline and Week 6

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted1 Dec 2025
  2. Study start1 Dec 2025 (estimated)
  3. Primary completion30 Jan 2026 (estimated)
  4. Study completion15 Feb 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
a randomized, controlled, assessor-blind, prospective study
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
30 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07255794
Sponsor's protocol ID
MU-FHP-DNS-TS-2025-02
Acronym
TK-DNS-TS
Status last verified
Nov 2025
First submitted
20 Nov 2025
Last updated
1 Dec 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Dynamic Neuromuscular Stabilization Exercises and Thoracic Stabilization Exercise in people with Kyphosis, run by Esra BECENI at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 1 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Esra Beceni, Lecturer (+905387358097, esra.beceni@mudanya.edu.tr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Thoracic Kyphosis Index (Flexible Ruler Measurement) (time frame: Baseline and Week 6). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Dec 2025.

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