Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID07350681

Evaluation of the Effects of Orthognathic Surgery on Plantar Pressure Distribution and Posture

Led by Ayşenur Dindar · Updated on 2026-01-20

60

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating how orthognathic surgery, which changes the three-dimensional position of the jaws, affects head and neck posture along with overall body posture. The study focuses on how these postural changes influence plantar pressure distribution. By comparing patients who undergo orthognathic surgery with non-operated individuals, the study aims to understand the direction and magnitude of these changes and their implications for postoperative evaluation and rehabilitation. The study includes 60 participants divided into two groups: 30 patients scheduled for orthognathic surgery and 30 control patients who have completed orthodontic treatment without surgery. The surgical group will undergo static and dynamic computerized plantar pressure analyses using specialized pedobarography systems before surgery and at a 6-month postoperative follow-up. Total body posture will be analyzed with a mobile application using four-directional photographs. Body height, weight, and lateral cephalometric radiographs will also be collected preoperatively and at the 6-month follow-up. The control group will receive comparable assessments during routine follow-up visits. Participants will be evaluated through posture and plantar pressure measurements before and after surgery or at corresponding times for controls. Data collected include body measurements, radiographs, and computerized pressure analyses to measure changes over time. Researchers will compare baseline and follow-up results to assess postural and plantar pressure changes. The study will help identify important parameters for patient rehabilitation after orthognathic surgery, with total participation lasting at least six months post-surgery or follow-up.

CONDITIONS

Brief Title

Effect of Orthognathic Surgery on Plantar Pressure and Posture

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Individuals aged 18 years or older at enrollment
  • Scheduled for single-jaw or double-jaw orthognathic surgery with comprehensive orthodontic treatment (study group)
  • Currently receiving orthodontic therapy with clear aligners or fixed appliances
  • Availability of preoperative lateral cephalometric radiographs
  • Completion of at least 6 months of postoperative orthodontic treatment (study group)
  • Body Mass Index (BMI) less than 30 kg/m²
  • Individuals not undergoing orthognathic surgery during the study period (control group)
  • No participation in physical or rehabilitative programs affecting posture or plantar pressure during the study (control group)
Not Eligible

You will not qualify if you...

  • Neuromuscular, musculoskeletal, or postural disorders affecting balance or plantar pressure
  • History of previous orthognathic or maxillofacial surgery
  • Systemic diseases affecting bone metabolism, neuromuscular function, or gait
  • Pregnancy
  • Inability or unwillingness to comply with study procedures or follow-up assessments

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Orthognathic Surgery

Duration - Surgery and postoperative orthodontic treatment period

Participants in the surgery group undergo orthognathic surgery with postoperative orthodontic treatment.

Surgery day plus routine postoperative care visits

Assessment Visits

Duration - Baseline and 6 months post-surgery or follow-up

Participants have static and dynamic computerized plantar pressure analyses, total body posture analysis, body height and weight measurements, and lateral cephalometric radiographs at baseline and 6 months post-surgery or follow-up.

2 visits (baseline and 6-month follow-up, in-person)

Trial Site Locations

Total: 1 location

1

Bezmialem Vakif University Faculty of Dentistry, Department of Orthodontics

Istanbul, Fatih, Turkey (Türkiye), 34093

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Research Team

A

Aysenur Dindar, PhD student

Ş

Şerife Şahin, Assistant Professor

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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