Skip to main content
Clinical Trials/NCT05802953
NCT05802953RecruitingNot Applicable

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

Afyonkarahisar Health Sciences University1 site in 1 country67 target enrollmentStarted: November 2, 2022Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
67
Locations
1
Primary Endpoint
Quality of life scores

Study Overview

Brief 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.

Detailed 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.

Study Design

Study Type
Observational
Observational Model
Other
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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

Outcomes

Primary Outcomes

Quality of life scores

Time Frame: 10 minutes

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.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Afyonkarahisar Health Sciences University
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Emel Taşvuran Horata

PhD; Assistant Professor

Afyonkarahisar Health Sciences University

Study Sites (1)

Loading locations...

Similar Trials