Skip to content

The Influence of a Stabilization Splint on the Body Posture

The Influence of of a Stabilization Splint on the Body Posture in TMD Cases and Controls

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00154128
Enrollment
40
Registered
2005-09-12
Start date
2005-04-30
Completion date
2005-08-31
Last updated
2005-11-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Arthromyalgia, Chronic Disease, Craniomandibular Disorders, Occlusal Appliance, Temporomandibular Disorders

Keywords

temporomandibular disorder, craniomandibular disorder, occlusal appliance, clinical trial

Brief summary

The study was designed to investigate a possible influence of an occlusal stabilization splint on the body posture in TMD cases and controls. Interocclusal appliances or occlusal splints are therapeutic devices that are most frequently used in the treatment of TMD. Changes of the mandibular position and occlusal equilibrations are assumed to have an impact on the general body posture.

Detailed description

Thirty TMD cases and 10 controls were included in the study. All participants were recruited from the School of Dentistry, University of Greifswald. All subjects gave their written consent to participate in the study. They then completed a TMD history questionnaire and underwent a clinical examination. The examination included palpation of the masticatory muscles and the TMJs, range of mandibular motion measurements, and assessment of joint noises. The TMD cases were required to have a diagnoses of myofascial pain and/or arthralgia. Controls had to be free of pain symptoms in their masticatory muscles and TMJs. Body posture was measured during five minutes of walking using an ultrasound-distance measuring device (sonoSens® Monitor) with small sensors placed on the skin that continually record changes in the distance between them. A static posture evaluation was performed with a contactless, and radiation-free static measurement of the back surface and spine using a 3D measurement system (formetric II). A second measurement was performed after insertion of the occlusal appliance and a third one after 7 days of treatment. The occlusal appliances were inserted after the first examination and all participants were instructed to use it at night and during examinations.

Interventions

Sponsors

University Medicine Greifswald
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* TMD cases: diagnoses of myofascial pain and/or arthralgia

Exclusion criteria

* TMD cases: chronic systemic diseases, cardiac pacemakers

Design outcomes

Primary

MeasureTime frame
changes in body posture

Secondary

MeasureTime frame
score of compliants
number of tender muscles and TMJs

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026