Examining quality of life in patients with temporomandibular joint dysfunction
Investigation of the Relationship of Individual, Physical and Psychosocial Characteristics With Quality of Life in Temporomandibular Joint Dysfunction
Afyonkarahisar Health Sciences University · NCT05802953
This study looks at how temporomandibular joint dysfunction affects the daily lives and well-being of people dealing with this condition.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 67 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Afyonkarahisar Health Sciences University (other) |
| Locations | 1 site (Afyonkarahisar) |
| Trial ID | NCT05802953 on ClinicalTrials.gov |
What this trial studies
This observational study aims to explore the relationship between quality of life and the individual physical and psychosocial characteristics of patients suffering from temporomandibular joint dysfunction (TMD). It builds on previous findings that indicate individuals with TMD experience a significantly lower quality of life compared to healthy individuals. The study will involve physical assessments and questionnaires to gather comprehensive data on the participants' experiences and challenges related to TMD. By identifying these characteristics, the study seeks to enhance understanding of how TMD impacts patients' lives.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18-65 who are classified as group I according to the RDC/TMD Axis I criteria.
Not a fit: Patients who have received treatment for TMD in the last six months or have other dental or related disorders may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved management strategies for TMD that enhance patients' quality of life.
How similar studies have performed: While there have been studies on TMD and quality of life, this specific focus on psychosocial aspects is relatively novel and may provide new insights.
Eligibility criteria
Show full inclusion / exclusion criteria
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
Where this trial is running
Afyonkarahisar
- Emel Taşvuran Horata — Afyonkarahisar, Turkey (RECRUITING)
Study contacts
- Principal investigator: EMEL TAŞVURAN HORATA, PhD — Afyonkarahisar Health Sciences University
- Study coordinator: EMEL TAŞVURAN HORATA, PhD
- Email: ethorata@gmail.com
- Phone: +905547759663
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Temporomandibular Joint Dysfunction Syndrome, Quality of Life