Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID07022795

Effectiveness of an Ecological Momentary Assessment Intervention to Reduce Masticatory Muscle Activity in Individuals at Risk for Temporomandibular Disorders

Led by University of Toronto · Updated on 2025-06-15

32

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the use of ecological momentary assessment (EMA) interventions combined with structured information to reduce masticatory muscle activity in individuals at risk for temporomandibular disorders (TMD). TMD, a common cause of orofacial pain affecting the muscles of mastication and jaw joints, often leads to chronic pain and disability. This randomized clinical trial aims to determine if EMA interventions, delivered via mobile devices, can effectively decrease harmful oral behaviors such as tooth clenching and awake bruxism, compared to structured information alone. The study compares two groups: one receiving an educational video about oral behaviors and jaw muscle management, and another receiving the same video plus a 1-week EMA intervention involving multiple daily prompts on mobile phones to report real-time oral behaviors. The EMA approach intends to raise awareness and support behavior change by encouraging participants to reflect on their habits throughout the day. The trial is randomized and single-blinded, assessing short- and long-term effects on muscle activity. Participants will be monitored for changes in the frequency and duration of oral behaviors using portable electromyography and self-report questionnaires. Assessments focus on behavior frequency after the 1-week intervention and follow-up at one month. The study involves baseline education, daily EMA prompts for one week in the experimental group, and outcome measurements to evaluate effectiveness. The total study duration and follow-up periods are designed to observe both immediate and lasting impacts on masticatory muscle activity and related symptoms.

CONDITIONS

Brief Title

Behavioral Interventions for Controlling Oral Behaviors

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years or older
  • Individuals reporting a score of 25 or higher on the oral behavior checklist (OBC), assessing frequency of oral behaviors like teeth clenching and grinding
  • Ability to use a mobile phone or similar device for daily surveys
Not Eligible

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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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Behavioral Treatment

Duration - 1 week

Participants receive behavioral interventions aimed at reducing oral behaviors. One group watches an educational video only, while the other group watches the video and undergoes an ecological momentary assessment (EMA) involving multiple daily surveys to increase awareness of oral behaviors.

Multiple daily survey prompts via mobile phone during the intervention week

Follow-up

Duration - Up to 1 month after intervention

Participants are monitored after the intervention period to assess changes in the frequency and duration of oral behaviors.

1 to 2 follow-up visits depending on group assignment

Trial Site Locations

Total: 1 location

1

Faculty of Dentistry

Toronto, Ontario, Canada, M5G1G6

Actively Recruiting

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Research Team

I

Iacopo Cioffi Associate Professor, Principal investigator, DDS, PhD

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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