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Clinical Trials in Turkey / NCT07133035
Active, not recruiting Observational

Investigation of Respiratory Function in Bruxism

NCT07133035 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2024-10-15
Last updated
2025-08-20

Condition(s) studied

BruxismSleep

Investigational drug(s) / intervention(s)

Pulmonary function testFonseca Anamnestic IndexJenkins Sleep ScaleBerlin QuestionnaireHeadache Impact Test-6

Pulmonary function test: Participants' respiratory functions will be assessed in different positions with the Cosmed Pony Fx Digital Spirometer (11). Forced vital capacity (FVC), forced expiratory volume in one second (FEV1), the ratio of forced expiratory volume in one second to forced vital capacity (FEV1/FVC), and peak expiratory flow rate (PEF) will be determined during the pulmonary function test.

Fonseca Anamnestic Index: The questionnaire consists of 10 questions covering headaches, neck pain, temporomandibular joint pain, pain during chewing, parafunctional habits, malocclusion, and stress, and is scored as 10 (yes), 5 (sometimes), and 0 (no). The total score ranges from 0 to 100. A higher total score indicates an increased risk of temporomandibular joint problems.

Jenkins Sleep Scale: The Jennkis Sleep Scale consists of four questions that assess sleep problems over a 4-week period. Each question is scored from 0 to 5. The total score ranges from 0 to 20 and indicates increasing sleep disturbance.

Berlin Questionnaire: Berlin Questionnaire: The Berlin Questionnaire is a three-part assessment tool that assesses individuals' predisposition to sleep apnea. The first part contains five questions investigating snoring, the second part contains four questions investigating daytime sleepiness, and the third part contains two questions investigating hypertension and obesity. Each section is evaluated independently. Individuals who score 2 or higher in the first and second sections, and those who score 1 in the third section, are considered predisposed to sleep apnea. If two or more categories are positive, the participant is considered high risk for obstructive sleep apnea. If the participant scores two or more in the first and second categories, they are considered high risk. If blood pressure is high or BMI is above 30 kg/m2, the participant is considered high risk.

Headache Impact Test-6: Headache Impact Test-6: The Headache Impact Test-6 (HIT-6) is administered to identify activities individuals are unable to perform due to headaches and to determine the extent to which headaches impact daily life. This six-question questionnaire includes columns with increasing scores, from "never" to "always." Participants are asked to mark the box closest to their response. A high total score indicates that headaches negatively impact daily life.

Study summary

The aim of the study was to evaluate the respiratory functions, sleep quality and headache severity of individuals with bruxism and to compare them with the control group without bruxism.

Eligibility

Sex
ALL
Min age
18 Years
Max age
45 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Being between 18-45 years old Exclusion Criteria: * Receiving orthodontic or splint treatment * Having more than two missing teeth * Having undergone jaw, thoracic, or abdominal surgery within the last 6 months * Having a history of cervical and/or thoracic trauma * Having a neurological, systemic, and/or cardiopulmonary disease * Using sleeping pills * Having a diagnosis of psychiatric illness

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Atılım University Ankara Gölbaşı

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07133035 on ClinicalTrials.gov ↗ ← All trials in Turkey