NCT07170813

Brief Summary

This project aims to investigate the effects of different hyperextension braces (Jewett and Spinomed) on spinal mobility and posture. Hyperextension braces are commonly prescribed to limit spinal flexion and regulate load distribution, especially in cases of spinal injuries and postural disorders. However, their objective impact on spinal biomechanics remains unclear. Purpose and Scope The study will be conducted on 30 healthy participants aged 18-35. Spinal mobility, posture, and movement analysis will be assessed using a dual inclinometer and the PostureScreen mobile application. Evaluations will be performed under three conditions:

  • Without a brace
  • With a Jewett brace
  • With a Spinomed brace (applied in randomized order) Assessments will include four-direction spinal mobility and postural analysis during daily life activities such as standing, squatting, and single-leg stance. Hypotheses H0: Hyperextension braces do not restrict spinal mobility. H1: Hyperextension braces restrict spinal mobility. H2: Hyperextension braces do not alter body alignment during movements. H3: Hyperextension braces alter body alignment during movements. Methodology The study is designed as a cross-sectional trial. Each measurement will be repeated three times. Data will be analyzed statistically using ANOVA or Kruskal-Wallis tests depending on distribution. Ethical approval has been obtained (Yalova University, Protocol No: 2024/4). Expected Contributions Academic: Results are expected to be presented at the Congress of the International Society of Biomechanics (2025) and published in a high-impact Q1 journal such as Spine. Clinical: Findings will provide objective data on the effectiveness of hyperextension braces, guiding clinicians and physiotherapists in brace selection. Educational: The project will also contribute to the training of young researchers, offering hands-on experience in research design and execution

Trial Health

75
On Track

Trial Health Score

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

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
4mo left

Started Oct 2025

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

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 Progress66%
Oct 2025Aug 2026

First Submitted

Initial submission to the registry

August 11, 2025

Completed
1 month until next milestone

First Posted

Study publicly available on registry

September 12, 2025

Completed
19 days until next milestone

Study Start

First participant enrolled

October 1, 2025

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2025

Completed
11 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 30, 2026

Expected
Last Updated

September 12, 2025

Status Verified

September 1, 2025

Enrollment Period

Same day

First QC Date

August 11, 2025

Last Update Submit

September 6, 2025

Conditions

Keywords

Posturemovementbiomechanicscorsetspine

Outcome Measures

Primary Outcomes (1)

  • Spinal Mobility (Range of Motion)

    Sppinal ROM in flexion, extension, and lateral flexions will be measured using dual inclinometers to assess the impact of each brace.

    11 months

Secondary Outcomes (1)

  • Postural Alignment Scores via PostureScreen App

    11 months

Study Arms (2)

Spinomed

EXPERIMENTAL

In this study, the effects of the Spinomed brace on spinal mobility will be evaluated. Participants will be fitted with the Spinomed brace for a defined period, and spinal range of motion will subsequently be assessed. Measurements will be performed using the dual inclinometer method, which provides an objective and reliable evaluation of spinal movements, including flexion, extension, lateral flexion, and rotation. The data obtained will be analyzed to determine the impact of the Spinomed brace on spinal mobility and to contribute to evidence-based clinical practice.

Other: Spinal hyperextension brace

Jewett

EXPERIMENTAL

In this study, the effects of the Jewett brace on spinal mobility will be evaluated. Participants will be fitted with the Jewett brace for a defined period, and spinal range of motion will subsequently be assessed. Measurements will be performed using the dual inclinometer method, which provides an objective and reliable evaluation of spinal movements, including flexion, extension, lateral flexion, and rotation. The data obtained will be analyzed to determine the impact of the Jewett brace on spinal mobility and to contribute to evidence-based clinical practice.

Other: Spinal hyperextension brace

Interventions

The Jewett brace is a hyperextension spinal orthosis designed to limit spinal flexion and promote proper posture by applying anterior and posterior forces to the thoracolumbar spine. It is commonly used for spinal fractures, postural disorders, and to reduce spinal load. Participants will wear the Jewett brace during the intervention phase, and spinal mobility and posture will be assessed.

JewettSpinomed

Eligibility Criteria

Age18 Years - 35 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Healthy young adults aged 18-35.
  • Body mass index (BMI) between 18.5 and 24.9 kg/m2

You may not qualify if:

  • Having experienced pain, discomfort, or discomfort in the upper back, waist, or lower extremities in the last 4 weeks on the Nordic Musculoskeletal System Questionnaire.
  • A score above 20 on the Oswestry Disability Questionnaire.
  • Having a condition related to spinal malalignment identified by a specialist physician (such as scoliosis, hyperkyphosis, hypokyphosis, Schuerman's kyphosis).
  • Having a history of congenital hip dislocation.
  • Having had surgery on the lower extremities or spine.
  • Having a neurological disease or medication use that could cause balance loss.
  • Having engaged in regular exercise in the last 6 months.
  • Having a history of regular brace use in the last 6 months.
  • Having a rheumatic disease affecting the axial skeleton.
  • Having a diagnosis of a disease related to the axial skeleton, such as spondylosis, spondylolisthesis, spinal stenosis, or disc herniation.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Yalova

Yalova, Turkey (Türkiye)

Location

Study Officials

  • Zeynep İclal Sag

    University of Yalova

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Research assisstant

Study Record Dates

First Submitted

August 11, 2025

First Posted

September 12, 2025

Study Start

October 1, 2025

Primary Completion

October 1, 2025

Study Completion (Estimated)

August 30, 2026

Last Updated

September 12, 2025

Record last verified: 2025-09

Data Sharing

IPD Sharing
Will not share

Locations