Telerehabilitation Dual-Task Training in Temporomandibular Joint Dysfunction

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.

NCT Number	NCT07556510
Lead Sponsor	Ege University
Conditions	Temporomandibular Joint Dysfunction
Enrollment	30 participants
Start Date	2026-06-16
Primary Completion	2026-10-16 (estimated)
Study Completion	2027-02-16 (estimated)
Updated on ClinicalTrials.gov	2026-05-05