The Effect of Bruxism on Balance
The Effect of Bruxism on Dynamic Balance in Desk Workers
1 other identifier
observational
54
1 country
1
Brief Summary
This study will investigate the effect of bruxism on dynamic balance in desk-bound individuals. Participants will be divided into two groups based on whether they are diagnosed with bruxism or not. Dynamic balance and proprioception will be compared between individuals from each group.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Dec 2025
Shorter than P25 for all trials
1 active site
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
First Submitted
Initial submission to the registry
December 15, 2025
CompletedFirst Posted
Study publicly available on registry
December 29, 2025
CompletedStudy Start
First participant enrolled
December 31, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 27, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
March 30, 2026
CompletedJanuary 15, 2026
December 1, 2025
2 months
December 15, 2025
January 13, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (9)
Short Form 36 (SF-36)
Quality of Life Scale/Short Form-36 (SF-36): SF-36 was developed by the Rand Corporation to obtain information about the health status of the individual. It was translated into Turkish by Koçyiğit and his colleagues, who conducted a validity and reliability study. It consists of eight sub-dimensions and 36 items. The sub-dimensions consist of physical function, social function, physical role difficulty, emotional state difficulty, mental health, energy/vitality, pain, and general perception of health. A score of "0" represents the worst health status, while "100" represents the best health status. Each sub-dimension is evaluated individually without calculating the total score.
Single assessment during study visit (1 day)
Pittsburgh Sleep Quality Index
Pittsburgh Sleep Quality Index (PSQI): It is a 24-question scale developed by Buysse et al. in 1989 that evaluates sleep quality in the last month. A Turkish validity and reliability study was performed in 1996. The sum of the scores of seven components, subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbance, sleep medication use, and daytime dysfunction, gives the total score index. The total PSQI score ranges from 0 to 21; a score above 5 points indicates poor sleep quality; a score of 5 points or less indicates good sleep quality. The PSQI is one of the most commonly used scales for evaluating sleep quality. The validity of the use of this index in sleep disorders has been tested before, and it has been frequently used in studies on bruxism.
Single assessment during study visit (1 day)
Beck Anxiety Inventory (BAI)
This scale's 21 items describe the most typical symptoms of anxiety disorders. It was developed to measure the intensity of anxiety symptoms in clinical populations. It asks respondents to indicate how much they have been affected by each symptom during the last week, on a scale from 0 (Not at all) to 3 (Severely - I could barely stand it). Total scores are the sum of all item scores, and range from 0 to 63; higher scores indicate higher anxiety. When this instrument was developed, the goal was to more easily discriminate between anxiety disorders and depressive disorders, whose symptoms frequently overlap on other assessment tools.
Single assessment during study visit (1 day)
Fonseca Anamnestic Index
Fonseca Anamnestic Index (FAI): It was developed in 1994 by Fonseca et al. and consists of 10 questions investigating pain in the head and TMJ. Turkish validity and reliability of the test was performed by Kaynak et al. The questionnaire includes various questions about joint, head, and neck pain; joint movements; parafunctional habits; impaired occlusion; and emotional stress. Participants were asked to answer "Yes" , "Sometimes" , or "No" to each question, and TMD was classified as none, mild, moderate, or severe according to the total score.
Single assessment during study visit (1 day)
Pain level-Visual Analog Scale (VAS)
Pain level-Visual Analog Scale: A visual analog scale (VAS) was used to assess the severity of pain related to bruxism. A VAS line was drawn on a 10 cm long horizontal line (0 = no pain and 10 = most intense pain), and the patient was asked to mark the pain intensity they perceived at rest, active use, and at night on this VAS line.
Single assessment during study visit (1 day)
Trigger Point Evaluation
Trigger points in trapezius, masseter and temporalis muscles will be evaluated by algometre. Sudden reaction or vocal response of the patient with light pressure applied to this point and the presence of reflected pain in a region distant from this region indicated the presence of a trigger point (the minimum and maximum pressure sensitivity range varies from person to person, as it differs in sensitivity).
Single assessment during study visit (1 day)
Perceived Stress Scale
Perceived Stress Scale: It was developed by Cohen, Kamarck, and Mermelstein in 1983 and consists of 14 items. Its Turkish validity and reliability was performed by Eskin et al., and this scale has been used in many studies on bruxism. The scale consists of two subdimensions: stress/discomfort perception and self-efficacy perception. Participants rate the stress they perceive on the scale as "0" never, "1" almost never, "2" sometimes, "3" often, and "4" very often. The stress level perceived by individuals is determined by summing the scores obtained from the items. A score between 0-56 points is obtained from the scale, and the higher the score, the higher the perceived stress level.
Single assessment during study visit (1 day)
Measurement of dynamic balance
Balance assessments will be performed using Computerized Posturography (ProKin 252, Tecnobody, Dalmine, Italy), this device provides objectively measurable data for balance measurements. TecnoBody Prokin 252 will be used to measure and evaluate the patient's dinamik balance and proprioception levels in detail.
Single assessment during study visit (1 day)
Evaluation of the Masseter's muscle stiffness
Masseter's muscle stiffness will be assessed with MyotonPRO. MyotonPRO (Muomeetria Ltd., Tallinn, Estonia) is a hand-held device used to quantify muscle stiffness. This device operates by generating a mechanical impulse on the skin overlying the muscle being assessed, followed by MyotonPRO measurements of the mechanical oscillations of muscles produced by the mechanical impulse. This method can determine the resistance of the muscle to deforming forces or muscle stiffness.
Single assessment during study visit (1 day)
Study Arms (2)
Bruxism group
Bruxism group: Adults aged 18-50 years who have bruxism symptoms. Participants will undergo assessments of Masseter muscle stiffness, trigger points, quality of life, sleep quality, and dynamic balance. No experimental interventions are assigned.
Non-bruxism group
Non-bruxism group: Adults aged 18-50 years those who do not have bruxism symptoms. Participants will undergo assessments of Masseter muscle stiffness, trigger points, quality of life, sleep quality, and dynamic balance. No experimental interventions are assigned.
Eligibility Criteria
This study will include adults aged 18-50 years old, Participants will be divided into two groups based on whether they're diagnosed with bruxism or not. Each group will contain 27 individuals. All participants must be able to follow instructions clearly and complete the study assessments.
You may qualify if:
- Age between 18 and 50 years,
- Participants must be diagnosed with bruxism by a dentist,
- Voluntary participation and signing the informed consent form,
- The participant must have the cognitive capacity to communicate and understand instructions,
- Desk work hours must be at least 4 hours.
You may not qualify if:
- Unable to cooperate,
- Having active inflammatory arthritis,
- Having had hip or knee surgery within the last 3 months,
- Having a diagnosed psychiatric illness,
- Having dentofacial anomalies,
- Being pregnant,
- Having a physical or cognitive condition that would prevent completion of the given test protocols,
- Inability to comply with or cooperate with test procedures during the measurement period.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
İstinye University
Istanbul, 34522, Turkey (Türkiye)
Related Publications (17)
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PMID: 26055653BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 15, 2025
First Posted
December 29, 2025
Study Start
December 31, 2025
Primary Completion
February 27, 2026
Study Completion
March 30, 2026
Last Updated
January 15, 2026
Record last verified: 2025-12