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Completed

NCT Number: NCT07827495

Synchronous vs Asynchronous Telerehabilitation for Bruxism

The goal of this clinical trial was to learn if online exercise and self-massage programs could lower pain and improve jaw movement in adults with bruxism (teeth grinding or clenching). The main questions it aimed to answer were:

Did live video exercise guided by a physical therapist lower jaw pain more than an independent video exercise program? Did live video exercise guided by a physical therapist improve mouth opening more than an independent video exercise program? Researchers compared live video sessions to independent video exercises to see which approach worked better for improving jaw function, sleep quality, and daily life.

Participants:

Completed an 8-session exercise and self-massage program over 4 weeks (2 times each week).

Either practiced live with a physical therapist over video calls or followed recorded video exercises on their own at home.

Answered surveys about pain, sleep quality, and oral health before and after the 4-week program.

Had their mouth opening, jaw muscle sensitivity, and muscle activity tested before and after the program.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Ankara University, Faculty of Dentistry

Ankara, Turkey (Türkiye)

About this study

Bruxism is characterized by repetitive masticatory muscle activity leading to masticatory muscle pain, restricted mandibular range of motion, and impaired oral health-related quality of life. Telerehabilitation represents a promising alternative to conventional face-to-face physiotherapy to overcome accessibility barriers.

In this prospective, randomized, two-arm parallel-group controlled trial, individuals diagnosed with clinically-based bruxism were randomly assigned to either the Synchronous Telerehabilitation Group (S-TRG) or the Asynchronous Telerehabilitation Group (A-TRG).

Both groups completed an 8-session intervention protocol over 4 weeks (2 sessions per week). The intervention protocol comprised:

Breathing training protocol (deep diaphragmatic breathing), Cervical region stretching and chin-tuck exercises, Temporomandibular joint range of motion and stretching exercises, Bilateral self-massage techniques (sliding, kneading, friction, and ischemic compression to masseter and temporalis muscles), Scapular stabilization exercises (W, T, and Y exercises).

In the S-TRG, sessions were conducted in real time under the direct supervision of a physiotherapist via live video calls. In the A-TRG, participants were taught the exercises in an initial recorded live video session and subsequently performed the protocol independently using their personalized instructional video recordings, with weekly phone/text check-ins to monitor adherence and screen for adverse events. Additionally, all participants received a standardized patient education brochure on TMJ care and behavioral modifications.

Outcome assessments were conducted at baseline and immediately following the 4-week intervention period. Evaluated parameters included:

Pain intensity assessed using the 0-10 Numeric Rating Scale (NRS) at rest, during the night, in the morning, and during activity, Maximum mouth opening (MMO) measured with a caliper, Pressure pain threshold (PPT) and pressure pain tolerance (PPTol) of the masseter and temporalis anterior muscles assessed using a digital algometer, Masticatory muscle activation during maximum voluntary isometric contraction and clenching tasks assessed via surface electromyography (sEMG), Oral health-related quality of life evaluated using the 14-item Oral Health Impact Profile (OHIP-14), Subjective sleep quality assessed using the Pittsburgh Sleep Quality Index (PSQI).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosed with clinically-based bruxism
  • Aged 18 years or older
  • Voluntarily agreed to participate and provided written informed consent

Exclusion criteria

  • Prior or concurrent neurological, psychiatric, or systemic diseases
  • Ongoing dental treatment
  • Currently receiving physical therapy
  • Regular use of medications such as analgesics or muscle relaxants
  • History of surgery or trauma involving the temporomandibular joint (TMJ) or neck region
  • Pregnancy
  • Active cancer
  • Planned surgical procedures
  • Visual, auditory, or cognitive impairments that could potentially confound the study outcomes
  • History of receiving treatment for the TMJ within the preceding 3 months

Treatment and study plan

Synchronous Telerehabilitation Protocol

Behavioral

Real-time video-supervised protocol consisting of diaphragmatic breathing, cervical stretching, TMJ range of motion and self-stretching, bilateral masseter/temporalis self-massage, scapular stabilization exercises, and TMJ education brochure (8 sessions over 4 weeks).

Asynchronous Telerehabilitation Protocol

Behavioral

Video-recorded home protocol consisting of identical diaphragmatic breathing, cervical stretching, TMJ range of motion/self-stretching, bilateral self-massage, scapular exercises, and TMJ education brochure performed independently with weekly check-ins (8 sessions over 4 weeks).

Primary outcomes

  1. Change in Pain Intensity

    Time frame: Baseline and post-intervention (Week 4)

    Assessed using the Numeric Rating Scale (NRS), an 11-point scale ranging from 0 (no pain) to 10 (worst possible pain). Pain intensity is evaluated at rest, during the night, in the morning upon waking, and during jaw activity/function.

Secondary outcomes

  1. Change in Maximum Mouth Opening (MMO)

    Time frame: Baseline and post-intervention (Week 4)

    Maximum active mouth opening without pain measured in centimeters (cm) using a caliper between the incisal edges of the maxillary and mandibular central incisors.

  2. Change in Pressure Pain Threshold (PPT)

    Time frame: Baseline and post-intervention (Week 4)

    Assessed in pounds (lb) using a digital algometer (1 cm² probe) over the bilateral masseter and anterior temporalis muscles to determine the minimum force at which pressure sensation transitions into pain.

  3. Change in Pressure Pain Tolerance (PPTol)

    Time frame: Baseline and post-intervention (Week 4)

    Assessed in pounds (lb) using a digital algometer (1 cm² probe) over the bilateral masseter and anterior temporalis muscles to determine the maximum level of pressure pain tolerated.

  4. Change in Masticatory Muscle Activity (sEMG)

    Time frame: Baseline and post-intervention (Week 4)

    Assessed via surface electromyography (sEMG) to evaluate muscle activation of the masseter and temporalis anterior muscles during maximum voluntary isometric contraction (MVIC) and clenching tasks.

  5. Change in Oral Health-Related Quality of Life (OHIP-14)

    Time frame: Baseline and post-intervention (Week 4)

    Evaluated using the Oral Health Impact Profile-14 (OHIP-14). Total scores range from 0 to 56, with higher scores indicating poorer oral health-related quality of life.

  6. Change in Subjective Sleep Quality (PSQI)

    Time frame: Baseline and post-intervention (Week 4)

    Assessed using the Pittsburgh Sleep Quality Index (PSQI). The global score ranges from 0 to 21, with scores greater than 5 indicating poor sleep quality.

Sponsors and collaborators

Lead sponsor

Gazi University

Other

Registry information

Official study title

Synchronous vs Asynchronous Telerehabilitation for Bruxism: A Randomized Controlled Trial

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Sep 18, 2026
Registry last updated
Sep 18, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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