Quality of Life in Temporomandibular Joint Dysfunction

Temporomandibular Joint Dysfunction Syndrome Clinical Trial

Official title:

Investigation of the Relationship of Individual, Physical and Psychosocial Characteristics With Quality of Life in Temporomandibular Joint Dysfunction

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05802953
• Other study ID #: 2022/5
• Status: Recruiting
• Start date: November 2, 2022
• Est. completion date: December 25, 2024

Study information

• Verified date: December 2023
• Source: Afyonkarahisar Health Sciences University
• Contact: EMEL TASVURAN HORATA, PhD
• Phone: +905547759663
• Email: ethorata[@]gmail.com
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

It is planned to examine the relationship between quality of life in patients with temporomandibular joint dysfunction and the patient's individual, physical and psychosocial characteristics.

Description:

A recent study showed that individuals with TMD have a lower quality of life than healthy controls. In addition, it was determined in the study that investigating the quality of life is insufficient. Future studies should search for psychosocial aspects related to TMD. The aim of this study is to individual the physical and psychosocial characteristics of individuals with Axis I TMD and examine their relationship with quality of life.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 67
• Est. completion date: December 25, 2024
• Est. primary completion date: December 25, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Being between the ages of 18-65,
• Being in group I according to RDC/TMD Axis I,

Exclusion Criteria:

• Any treatment for temporomandibular joint dysfunction (TMD) in the last six months
• Having dental problems
• Having any disorder and/or disease involving structures and/or masticatory muscles associated with TMD
• Having a history of trauma in the head and neck region,
• Having previously undergone temporomandibular joint surgery,
• Using corticosteroid and anticonvulsant drugs
• Patients who have received physiotherapy and rehabilitation related to the temporomandibular joint in the last six months

Related Conditions & MeSH terms

• Joint Diseases
• Temporomandibular Joint Disorders
• Temporomandibular Joint Dysfunction Syndrome

Intervention

Other:
• Physical assessments
Physical assessments include the presence of joint sounds (yes/no), Fonseca Anamnestic Questionnaire, tenderness/pressure pain threshold rating, muscle strengths assessments, temporomandibular joint and cervical region range of motion measurements, and pain.
• Questionnaire
General Health Questionnaire-28 and SF-36 will be apply.

Locations

Country	Name	City	State
Turkey	Emel Tasvuran Horata	Afyonkarahisar

Sponsors (1)

Lead Sponsor	Collaborator
Afyonkarahisar Health Sciences University

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Quality of life scores	The quality of life will be assess using SF-36. This questionnaire has 8 sections and 36 items. The sections evaluate health between 0-100 and the higher the score indicates the better the quality of life.	10 minutes