Dynamic Posture and Head Position in Kyphotic Female and Male (DPHP)

July 23, 2024 updated by: Gönül Elpeze, Gaziantep Islam Science and Technology University

Comparison of Dynamic Posture and Head Position in Kyphotic Individuals According to Gender

This study examined the comparison of dynamic posture and head position in kyphotic ındividuals according to gender.

Methods: A total of 54 female and male adolescents (between the ages of 12 and 18) with a thoracic kyphosis (TK) angle of ≥ 50° were divided into two groups according to gender.

The kyphosis angle, dynamic postural performance, and forward head position were measured using a flexible ruler, Mathiass test, and occiput wall distance.

Study Overview

Detailed Description

This study examined the comparison of dynamic posture and head position in kyphotic ındividuals according to gender.

Methods: This observational cross-sectional study was conducted with 54 subjects. Subjects aged 12 to 18 years with a kyphosis angle of ≥50º and the children and their parents who agreed to participate in the study were included. Individuals with Scheurmann kyphosis, scoliosis (Cobb angle >10°), and other congenital spine abnormalities were excluded.

The kyphosis angle was measured using a smartphone inclinometer. Dynamic posture was assessed using the Matthias test. Head position was obtained using occiput-wall distance.

Study Type

Observational

Enrollment (Actual)

54

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Gaziantep, Turkey
        • Gaziantep Islam Science and Technology University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

ADOLESCENT

Description

Inclusion Criteria:

  • Subjects with a kyphosis angle of ≥50º and the children and their parents who agreed to participate in the study were included.

Exclusion Criteria:

  • Individuals with Scheurmann kyphosis, scoliosis (Cobb angle >10°), and other congenital spine abnormalities were excluded.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Female
Thoracic kyphosis (TK) angle of ≥ 50° The kyphosis angle, dynamic postural performance, forward head position
The subject was positioned in a neutral standing position. the short side of the phone was placed on the T1-3 spinous process and the protractor was set to 0°. Subsequently, the phone was placed on the T12, and the angular value displayed on the screen was recorded as the kyphotic angle.
Other Names:
  • Thorasic kyphosis
The test measures spinal alignment deviations during static loading in the 90° shoulder flexion position. The test measurements are made in a standing position with arms 90° flexed, without weight, and after 30 seconds with weight.
Other Names:
  • Matthias Test
The individual stands with his heels and pelvis in contact with the wall. The severity of kyphosis is interpreted by measuring the distance between the occiput and the wall in cm with the head facing forward. The intensity of kyphosis is classified as mild (≤5 cm), moderate (5.1-8 cm) and severe (>8 cm)
Other Names:
  • Occiput-Wall Distance
Male
Thoracic kyphosis (TK) angle of ≥ 50° The kyphosis angle, dynamic postural performance, forward head position
The subject was positioned in a neutral standing position. the short side of the phone was placed on the T1-3 spinous process and the protractor was set to 0°. Subsequently, the phone was placed on the T12, and the angular value displayed on the screen was recorded as the kyphotic angle.
Other Names:
  • Thorasic kyphosis
The test measures spinal alignment deviations during static loading in the 90° shoulder flexion position. The test measurements are made in a standing position with arms 90° flexed, without weight, and after 30 seconds with weight.
Other Names:
  • Matthias Test
The individual stands with his heels and pelvis in contact with the wall. The severity of kyphosis is interpreted by measuring the distance between the occiput and the wall in cm with the head facing forward. The intensity of kyphosis is classified as mild (≤5 cm), moderate (5.1-8 cm) and severe (>8 cm)
Other Names:
  • Occiput-Wall Distance

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Matthias test
Time Frame: 1 year
Matthias test assesses dynamic postural performance
1 year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Occiput wall distance
Time Frame: 1 year
Occiput wall distance is an assessment method to determine forward head posture in clinical settings.
1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Gonul Elpeze, Asst. Prof., Gaziantep Islam Science and Technology University Physical Therapy and Rehabilitation Department

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 16, 2023

Primary Completion (Actual)

January 20, 2024

Study Completion (Actual)

June 5, 2024

Study Registration Dates

First Submitted

July 9, 2024

First Submitted That Met QC Criteria

July 23, 2024

First Posted (Actual)

July 26, 2024

Study Record Updates

Last Update Posted (Actual)

July 26, 2024

Last Update Submitted That Met QC Criteria

July 23, 2024

Last Verified

July 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • GIBSTU

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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