About this trial
This randomized controlled trial will be conducted among 18-25-year-old participants who present with temporomandibular joint dysfunction symptoms, including pain, limited range of motion, and joint crepitation. Participants will be randomly allocated into control and intervention groups using block randomization. The control group will receive a standard physiotherapy program, while the intervention group will additionally perform telerehabilitation-based dual-task exercises. The intervention will last for six weeks, with progressive increases in exercise and cognitive task difficulty. Outcomes will be assessed at baseline and at the end of the 6th week. Primary and secondary outcome measures include pain intensity (Visual Analog Scale), jaw functional limitation (Jaw Functional Limitation Scale-20), oral habits, static balance (Tetrax system), and dynamic balance (Timed Up and Go Test). Within-group and between-group comparisons will be performed. The sample size was calculated using power analysis, resulting in 30 participants in total (15 per group), accounting for potential dropouts.
Eligibility criteria
Qualifiers
Diagnosis of temporomandibular joint dysfunction according to the
Temporomandibular Disorders Research Diagnostic Criteria and Diagnostic
Criteria for Temporomandibular Disorders
No neurological, orthopedic, or systemic condition that may affect balance
Disqualifiers
Inability to participate in regular exercise or telerehabilitation programs
Presence of severe systemic diseases (cardiac, rheumatologic, neurological) or other severe chronic conditions
Presence of psychiatric disorders or cognitive impairment
Use of medications that may affect balance (such as sedatives)
Trial design
Treatments tested in this trial
- Standard Physiotherapy Program
- Dual-Task Training