Actively Recruiting
Somatosensory Training Versus Exercise Therapy in Awake Bruxism
Led by Aydin Adnan Menderes University · Updated on 2026-01-13
20
Participants Needed
2
Research Sites
50 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Somatosensory Training Versus Exercise Therapy in Awake Bruxism
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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 65/10 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
You will not qualify if you...
- GCPS Grade IV (high disability level)
- Presence of systemic inflammatory, neurological, or rheumatological disorders
- Diagnosis of severe chronic pain conditions unrelated to bruxism
- Use of occlusal splints or participation in jaw, neck, or facial therapy within the past 3 months
- Psychiatric disorders or cognitive impairment that could interfere with study participation
- Pregnancy, due to potential effects on joint laxity and postural parameters
AI-Screening
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Trial Site Locations
Total: 2 locations
1
Aydin Adnan Menderes University, Faculty of Health Sciences, Physiotherapy and Rehabilitation Unit
Aydin, Turkey (Türkiye), 09100
Actively Recruiting
2
Aydin Adnan Menderes University, Faculty of Health Sciences, Physiotherapy and Rehabilitation Unit
Aydin, Turkey (Türkiye), 09100
Actively Recruiting
Research Team
G
Gul Oznur Karabicak, Phd
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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