Actively Recruiting
Behavioral Interventions for Controlling Oral Behaviors
Led by University of Toronto · Updated on 2025-06-15
32
Participants Needed
1
Research Sites
85 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Ecological momentary assessment (EMA) interventions via mobile devices can be implemented to monitor an individual's negative health behaviors in real-time, increase awareness, and assist patients in overting those behaviors. In recent years, EMA interventions have been used to improve patients' awareness of specific oral behaviors, such as tooth clenching or awake bruxism, which can produce excessive forces on the muscles of mastication and lead to or exacerbate symptoms of temporomandibular disorders (TMD). Yet, whether EMA interventions are effective in reducing oral behaviors and masticatory muscle activity in the short- and long-term, or whether they are more effective than patient education remains unclear. In this randomized clinical trial, we aim to test the effects of a 1-week EMA intervention combined with structured information on masticatory muscle activity and determine whether a combined approach including an EMA intervention and structured information is more effective in reducing masticatory muscle activity than structured information alone. Our study will have a significant impact on orofacial pain clinical research as it will provide clinically relevant measures which could inform multimodal approaches for the management of painful TMD.
CONDITIONS
Official Title
Behavioral Interventions for Controlling Oral Behaviors
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Individuals aged 18 years or older
- Report a score of 25 or higher on the oral behavior checklist (OBC)
- Experience frequent daytime and sleep-related oral behaviors such as teeth clenching, grinding, or jaw tension
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
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Trial Site Locations
Total: 1 location
1
Faculty of Dentistry
Toronto, Ontario, Canada, M5G1G6
Actively Recruiting
Research Team
I
Iacopo Cioffi Associate Professor, Principal investigator, DDS, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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