Evaluation of Symptom Improvement through the Use of a Smartphone Application in Patients with Temporomandibular Disorder (TMD).

Not Applicable

Completed

• Conditions: Diseases of the digestive system

• Registration Number: KCT0008889
• Lead Sponsor: Seoul National University Bundang Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2022-06-24
• Last Update Posted: 13 November 2023

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

? Adults aged 19 to 65 years old.
? Patients diagnosed with temporomandibular disorder (TMD) who visited the Seoul National University Dental Hospital.
? Patients diagnosed with muscular disorders, temporomandibular joint internal derangements, and temporomandibular joint arthritis based on clinical and radiological examinations.
? Individuals who voluntarily decided to participate in this clinical trial and provided written consent.

Exclusion Criteria

? Individuals not diagnosed with temporomandibular disorder (TMD) based on clinical and radiological examinations.
? Individuals with intrinsic diseases of the temporomandibular joint: ankylosis, tumors.
? Individuals with traumatic conditions of the temporomandibular joint: mandibular condyle fractures, major facial trauma (e.g., from traffic accidents, assaults, etc.).
? Individuals suffering from rare muscular diseases such as severe myasthenia gravis, Eaton-Lambert syndrome, and amyotrophic lateral sclerosis.
? Individuals with serious metabolic diseases like severe hypertension or diabetes.
? Individuals diagnosed with neurological disorders (e.g., Parkinson's, Alzheimer's) or psychiatric disorders.
? Individuals currently taking medications for sleep disorders (e.g., benzodiazepines, muscle relaxants, tricyclic antidepressants, etc.), or potentially consuming unauthorized drugs, alcohol, or narcotics.
? Individuals undergoing dental orthodontics or wearing other oral devices.
? Cases where the participant withdraws their consent.
? Any other individuals deemed inappropriate for the study by the principal investigator.

Study & Design

• Study Type: Interventional Study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain : Numeric Rating Scale (NRS) ;Mouth opening (mm)

Secondary Outcome Measures

Name	Time	Method
Jaw Functional Limitation Scale (JFLS) -20;Oral Behavior checklist; Patient Health Questionnaire (PHQ) -4