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Effects of Occlusal Imbalance and Clenching on Balance in Stroke Patients

Effects of Stimulated Occlusal Imbalance and Jaw Clenching on Balance and Fall Risk in Stroke Patients

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07007429
Enrollment
60
Registered
2025-06-05
Start date
2025-05-15
Completion date
2025-07-22
Last updated
2026-02-11

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

Conditions

Stroke

Keywords

Balance

Brief summary

The aim of the study is to investigate the effects of stimulated occlusal imbalance and jaw clenching on balance and fall risk in patients with stroke.

Detailed description

This randomized controlled study will be conducted on a minimum of 42 stroke patients who meet the inclusion and exclusion criteria. Patients included in the study will be randomly assigned to one of three groups: the ipsilateral side stimulated occlusal imbalance group, the contralateral side stimulated occlusal imbalance group, or the bilateral jaw clenching group.

Interventions

OTHERIpsilesional Side Stimulated Occlusal Imbalance

In this group, a 1 cm thick cotton roll will be placed on the ipsilesional occlusal surfaces of the patients, and they will be instructed to hold it in place without clenching.

OTHERContralesional Side Stimulated Occlusal Imbalance

In this group, a 1 cm thick cotton roll will be placed on the contralesional occlusal surfaces of the patients, and they will be instructed to hold it in place without clenching.

OTHERBilateral Cotton Roll with Jaw Clenching

In this group, a 1 cm thick cotton roll will be placed on both occlusal surfaces, and the patients will then be instructed to clench their teeth.

Sponsors

Bitlis Eren University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

The evaluator and the researcher administering intervention will be different.

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Having chronic stroke, * A Mini-Mental State Examination score of 24 or higher, * Being between 18 and 75 years of age, * Having a Brunnstrom stage of 4 or above, * Ability to stand independently for 20 seconds or more, * Ability to walk independently for 10 meters, using assistive devices or orthoses if necessary, * Having opposing mandibular and maxillary second premolars or first molars

Exclusion criteria

* The presence of severe osteoarthritis in the lower extremity, * The presence of cancer or diabetic neuropathy, * The presence of vestibular disorder, * The presence of lower extremity ulceration or amputation, * Hemodynamic instability, * The presence of other neurological disorders (such as multiple sclerosis, Parkinson's disease), * Having experienced an acute lower extremity injury in the last six weeks, * History of lower extremity surgery, * Alcohol consumption in the last 24 hours * Posterior circulation stroke involving the basilar artery or cerebellum

Design outcomes

Primary

MeasureTime frameDescription
Overall Postural Stability Index MeasurementChange from baseline overall postural stability index immediately after the interventionThis index will be assessed by measuring deviations of the center of gravity in the anteroposterior and mediolateral directions. Lower scores indicate smaller deviations and better postural stability. The test will be performed on a stable platform with two trials of 30 seconds each. The average of the two trials will be automatically calculated by the TechnoBody balance system.
Fall Risk AssessmentChange from baseline fall risk immediately after the interventionFall risk will be assessed by measuring the patient's ability to maintain balance on an unstable platform. Based on their ability to maintain balance, a fall risk score will be generated, with higher scores indicating a greater risk of falling. The test will be performed with two 30-second trials. The average of the two trials will be calculated automatically by the TechnoBody balance system.

Secondary

MeasureTime frameDescription
Anteroposterior Stability Index MeasurementChange from baseline anteroposterior stability index immediately after the interventionThe anteroposterior stability index will be assessed by measuring deviations of the center of gravity in the anteroposterior direction. Lower scores indicate smaller deviations and better anteroposterior postural stability. The test will be performed on a stable platform with two trials of 30 seconds each. The average of the two trials will be automatically calculated by the TechnoBody balance system.
Mediolateral Stability Index MeasurementChange from baseline mediolateral stability index immediately after the interventionThe mediolateral stability index will be assessed by measuring deviations of the center of gravity in the mediolateral direction. Lower scores indicate smaller deviations and better mediolateral postural stability. The test will be performed on a stable platform with two trials of 30 seconds each. The average of the two trials will be automatically calculated by the TechnoBody balance system.
Weight Bearing Distribution AssessmentChange from baseline weight bearing distribution immediately after the interventionWeight-bearing distribution will be assessed by measuring the percentage of body weight borne by each limb during quiet standing. Lower asymmetry values indicate more balanced weight distribution and better postural stability. The test will be performed on a stable platform with two trials of 30 seconds each. The average of the two trials will be automatically calculated by the TechnoBody balance system.

Countries

Turkey (Türkiye)

Contacts

PRINCIPAL_INVESTIGATORömer dursun, Asst. Prof.

Bitlis Eren University

PRINCIPAL_INVESTIGATORburak mavuş, M.Sc.

Bolu Abant İzzet Baysal Physiotherapy and Rehabilitation Training and Research Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026