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Somatosensory Training Versus Exercise Therapy in Awake Bruxism: A Randomized Controlled Trial

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Awake bruxism (daytime teeth clenching or jaw tension) is a common condition that can cause jaw pain, facial pain, muscle fatigue, and reduced quality of life. Although current treatments often focus on the jaw muscles and posture, recent research suggests that changes in the brain's sensory processing may also play an important role in bruxism-related pain. This randomized controlled trial aims to compare two physiotherapy-based treatment approaches with a wait-list control group in adults with awake bruxism. Participants will be randomly assigned to one of three groups: (1) somatosensory awareness-based training, (2) jaw and posture exercise therapy, or (3) a wait-list control group. The somatosensory training program focuses on improving body awareness and sensory perception of the face and jaw, while the exercise program includes jaw mobility, postural alignment, and cervical exercises. Both active interventions will be delivered over a 4-week period. Participants will be assessed at baseline, immediately after treatment, and during follow-up to evaluate changes over time. The main outcome of this study is orofacial pain intensity. Secondary outcomes include jaw function, sensory processing, muscle structure, oral parafunctional behaviors, and oral health-related quality of life. The results of this study may help improve physiotherapy-based treatment strategies for people with awake bruxism by addressing both physical and sensory aspects of the condition.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 45
Healthy Volunteers: f
View:

• Adults aged 18 to 45 years

• Clinical diagnosis of awake bruxism confirmed using standardized diagnostic criteria (STAB and DC/TMD Axis I)

• Presence of at least one measurable somatosensory alteration confirmed at baseline using digital and clinical assessments

• Self-reported daytime jaw clenching or parafunctional activity

• Baseline orofacial pain intensity of ≥5/10 on a Visual Analog Scale (VAS)

• Chronic pain graded as GCPS Grades I-III according to DC/TMD Axis II (Turkish validated version)

• Willingness to comply with the study protocol and attend scheduled treatment sessions

• Ability to understand the study procedures and provide written informed consent

Locations
Other Locations
Turkey
Aydin Adnan Menderes University, Faculty of Health Sciences, Physiotherapy and Rehabilitation Unit
RECRUITING
Aydin
Aydin Adnan Menderes University, Faculty of Health Sciences, Physiotherapy and Rehabilitation Unit
RECRUITING
Aydin
Contact Information
Primary
Gul Oznur Karabicak, Phd
guloznur@gmail.com
+905053569409
Time Frame
Start Date: 2025-12-16
Estimated Completion Date: 2026-12
Participants
Target number of participants: 20
Treatments
Experimental: Somatosensory Awareness Training Group
Participants assigned to this group will receive a somatosensory retraining and patient education program based on CRAFTA principles. The intervention focuses on tactile and proprioceptive stimulation, body awareness, and body schema-oriented techniques, including tasks such as two-point discrimination training, light touch awareness, mirror-based posture observation, and self-monitoring of parafunctional behaviors. No conventional strengthening or mobility exercises will be provided. Participants will complete daily awareness-based home tasks, and adherence will be monitored weekly through brief structured follow-ups conducted by a research assistant.
Active_comparator: Jaw and Posture Exercise Group
Participants in this group will receive a structured physiotherapy program based on previously published protocols. The intervention includes jaw mobility and relaxation exercises, postural alignment and scapular stabilization exercises, and cervical stretching and strengthening exercises. Participants will attend supervised face-to-face sessions twice weekly for four weeks and will also receive a home exercise booklet.
Other: Wait-List Control Group
Participants in the wait-list group will not receive any active intervention during the first four weeks but will continue their usual daily routines. They will be assessed at the same time points as the intervention groups to allow comparison of natural symptom progression. After completion of the primary endpoint assessment, participants in this group will be offered an active intervention according to clinical need.
Related Therapeutic Areas
Sponsors
Leads: Aydin Adnan Menderes University

This content was sourced from clinicaltrials.gov