NCT07142538

Brief Summary

The thoracic curvature of the spinal column occurs in the sagittal plane. While the normal thoracic kyphosis angle of the spine is 20-40°, an angle of 45-50° is referred to as postural kyphosis, increased kyphosis, or hyperkyphosis. The strength of the central and deep back muscles of the trunk controls spinal stability and intervertebral movements in dynamic situations. This ensures that thoracic curvature is maintained within normal physiological limits. Increased kyphosis can result from poor postural habits, prolonged computer use, trunk asymmetry, and muscle weakness. Studies have reported an increase in thoracic kyphosis, postural deviations in the trunk, and changes in shoulder and head positions as a result of weakening of the back muscles. Corrective exercise programmes aimed at strengthening the back muscles are frequently used in the treatment of thoracic kyphosis. The effects of exercise programmes on muscle strength, endurance, and kyphosis angle have been investigated. However, there are few studies examining the effects of corrective exercise programmes on muscle tone and viscoelastic properties in the back muscles. In our study, we aim to investigate the effects of an 8-week corrective exercise programme on the tone and viscoelastic properties of the back muscles in individuals with thoracic kyphosis and to propose its inclusion as a contemporary approach in clinical treatment protocols.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
44

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Feb 2024

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2024

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2024

Completed
9 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 15, 2024

Completed
8 months until next milestone

First Submitted

Initial submission to the registry

August 19, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

August 26, 2025

Completed
Last Updated

August 26, 2025

Status Verified

August 1, 2025

Enrollment Period

2 months

First QC Date

August 19, 2025

Last Update Submit

August 25, 2025

Conditions

Outcome Measures

Primary Outcomes (3)

  • 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, stiffness, and elasticity, and it also offers high test-retest reliability and reproducibility .

    8 weeks

  • 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

    8 weeks

  • 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

    8 weeks

Study Arms (2)

corrective exercise group

ACTIVE COMPARATOR

8 weeks, 3 days a week, 45 minutes shoulder, neck and back exercises postur exercises

Other: exercises

control group

ACTIVE COMPARATOR

Shoulder and neck posture exercises Home exercises 8 weeks 3 days a week

Other: exercises

Interventions

Exercise training was provided to both groups.

control groupcorrective exercise group

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • having a kyphosis degree of ≥50° in individuals with thoracic kyphosis and voluntarily participating in the study.

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

SANKO University

Gaziantep, 27090, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Motor ActivityKyphosis

Interventions

Exercise

Condition Hierarchy (Ancestors)

BehaviorSpinal CurvaturesSpinal DiseasesBone DiseasesMusculoskeletal Diseases

Intervention Hierarchy (Ancestors)

Motor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
director

Study Record Dates

First Submitted

August 19, 2025

First Posted

August 26, 2025

Study Start

February 1, 2024

Primary Completion

April 1, 2024

Study Completion

December 15, 2024

Last Updated

August 26, 2025

Record last verified: 2025-08

Data Sharing

IPD Sharing
Will not share

Locations