BruxismMOD-SPNCT07364552
Patient-Specific Occlusal Splints Using MODJAW Kinematics
A study testing MODJAW-Based Patient-Specific Occlusal Splint and Standard Occlusal Splint in people with Bruxism, run by Istanbul University at 1 site in Turkey (Türkiye).
Trial summary
This clinical study is designed to evaluate the effectiveness of patient-specific occlusal splints created using MODJAW, a jaw-tracking device that records 3D mandibular movements. Read more about this study
- Who is it for?
- Ages 18 to 50 years
- Conditions the study is for
- Bruxism
- What is being tested?
- MODJAW-Based Patient-Specific Occlusal Splint and Standard Occlusal Splint
- Type of treatment
- Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 40 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 15 Oct 2025to 25 Dec 2025
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 50 years
- All sexes
- No healthy volunteers
- Adult
Who may be able to join
- Age 18-50 years
- Diagnosed with mild-to-moderate bruxism or temporomandibular joint (TMJ) dysfunction
- Willingness and ability to comply with splint use and study visits
- Signed informed consent
Who cannot join
- Severe dental loss or existing prosthetic devices interfering with splint placement
- Systemic medical conditions affecting jaw function
- History of TMJ trauma or surgery
- Pregnancy or breastfeeding
- Allergy to splint materials
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Patient-Specific Occlusal Splints Designed Using MODJAW Kinematic Data: A Prospective Clinical Study
This clinical study is designed to evaluate the effectiveness of patient-specific occlusal splints created using MODJAW, a jaw-tracking device that records 3D mandibular movements. Occlusal splints are commonly used to treat bruxism (teeth grinding) and temporomandibular joint (TMJ) disorders, which can cause jaw pain, headaches, and worn teeth. Traditional splints are made using standard designs that do not consider each patient's unique jaw movements.
In this study, 40 participants with mild-to-moderate bruxism or TMJ dysfunction will be randomly assigned to two groups. One group will receive custom splints designed using MODJAW kinematic data, while the other group will receive standard occlusal splints. Participants will use their assigned splint for 8 weeks.
Read more
The study will measure:
Jaw movement patterns using MODJAW
TMJ pain levels
Patient comfort and satisfaction
The main goal is to determine whether MODJAW-based, patient-specific splints provide better jaw function, reduced pain, decreased teeth grinding, and higher patient satisfaction compared to standard splints.
Participants will be monitored throughout the study to ensure safety, comfort, and proper splint use. This study is expected to help dentists design more effective, personalized splints in the future and improve treatment outcomes for people with jaw disorders or bruxism.
Read the detailed description
Detailed Description:
Background and Rationale:
Bruxism and temporomandibular joint (TMJ) disorders are common conditions that can lead to jaw pain, headaches, tooth wear, and impaired quality of life. Occlusal splints are commonly prescribed to manage these conditions by stabilizing the jaw and distributing occlusal forces. Standard splints, however, are typically fabricated using uniform designs that do not account for the individual jaw movement patterns of each patient. Recent advances in digital dentistry, including the use of jaw-tracking devices such as MODJAW, allow clinicians to capture three-dimensional mandibular kinematics in real time. By using this information, occlusal splints can be designed to match the specific movement patterns of each patient, potentially improving comfort, jaw function, and clinical outcomes.
This study aims to evaluate whether patient-specific occlusal splints designed using MODJAW kinematic data provide superior clinical outcomes compared to standard occlusal splints.
Study Objectives:
To compare mandibular movement patterns between MODJAW-based patient-specific splints and standard occlusal splints.
To evaluate the effect of MODJAW-based splints on bruxism frequency and intensity.
To assess TMJ pain reduction in participants using MODJAW-based splints versus standard splints.
To determine patient satisfaction and comfort with patient-specific versus standard splints.
Study Design:
This is a prospective, randomized, controlled interventional study. Forty participants with mild-to-moderate bruxism or TMJ dysfunction will be randomly assigned to one of two groups:
MODJAW group (n=20): Participants will receive a patient-specific occlusal splint designed based on 3D mandibular kinematic data collected with MODJAW.
Standard splint group (n=20): Participants will receive a conventional occlusal splint fabricated using standard methods.
The study duration for each participant is 8 weeks, during which participants will wear their assigned splints according to instructions and attend follow-up assessments.
Inclusion Criteria:
Age 18-50 years
Diagnosed with mild-to-moderate bruxism or TMJ dysfunction
Willingness and ability to comply with splint use and study visits
Signed informed consent
Exclusion Criteria:
Severe dental loss or existing prosthetic devices interfering with splint placement
Systemic medical conditions affecting jaw function
History of TMJ trauma or surgery
Pregnancy or breastfeeding
Allergy to splint materials
Study Procedures:
Screening and Baseline Assessment:
Clinical examination of dentition and TMJ
Recording baseline jaw movements using MODJAW (for both groups)
Baseline assessment of bruxism frequency, TMJ pain (VAS score), and patient-reported comfort
Splint Fabrication:
MODJAW group: CAD/CAM splints designed using mandibular movement data captured by MODJAW
Standard group: Conventional splints fabricated according to standard occlusal design
Splint Use:
Participants instructed to wear splints nightly (or as directed) for 8 weeks
Weekly check-ins to monitor compliance and comfort
Follow-Up Assessments (Week 4 and Week 8):
Repeat MODJAW recordings to evaluate changes in mandibular movement
Assess TMJ pain, bruxism frequency and intensity
Collect patient satisfaction and comfort scores via 5-point Likert scale
Record any adverse events
Outcome Measures:
Primary Outcome: Changes in mandibular movement patterns as measured by MODJAW
Secondary Outcomes:
Reduction in TMJ pain (VAS score)
Patient-reported satisfaction and comfort
Data Analysis:
Within-group comparisons: Paired t-tests or Wilcoxon signed-rank tests
Between-group comparisons: Mann-Whitney U test
Categorical outcomes: Chi-square or Fisher's exact test
Statistical significance set at p < 0.05
Safety Considerations:
Participants monitored for adverse events related to splint use, including discomfort, tissue irritation, or allergic reactions
Participants may withdraw at any time
All data handled according to confidentiality and privacy guidelines
Significance:
This study will provide evidence on the effectiveness of patient-specific, MODJAW-guided occlusal splints in improving jaw function, reducing bruxism, and increasing patient satisfaction. The results may support the adoption of kinematic data in routine occlusal splint design and contribute to personalized dentistry approaches.
- Conditions
- Bruxism
- Being tested
- MODJAW-Based Patient-Specific Occlusal Splint, Standard Occlusal Splint
- Keywords
- Occlusal splint
- Medical subject headings
- Bruxism
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
MODJAW-Based Patient-Specific Occlusal SplintDevice
A custom occlusal splint designed using MODJAW-recorded 3D mandibular movement data. Fabricated via CAD/CAM to fit the patient's unique jaw movements. Worn nightly (or per instructions) for 8 weeks.
Standard Occlusal SplintDevice
A conventional occlusal splint made using standard methods without patient-specific mandibular movement data. Worn nightly (or per instructions) for 8 weeks.
| Study group | Role | What they receive |
|---|---|---|
| MODJAW-Based Patient-Specific Splint | Experimental | Participants receive a patient-specific occlusal splint designed using MODJAW 3D mandibular kinematic data. The splint is fabricated via CAD/CAM and worn according to study instructions for 8 weeks. Receives: Device: MODJAW-Based Patient-Specific Occlusal Splint |
| Standard Occlusal Splint | Experimental | Participants receive a conventional occlusal splint fabricated using standard methods. The splint is worn according to study instructions for 8 weeks. Receives: Device: Standard Occlusal Splint |
What is being measured
The primary outcome is the main question the study is designed to answer.
Improvement in mandibular movement patterns
Mandibular movements will be recorded using MODJAW 3D jaw-tracking system.
Parameters include opening, lateral, and protrusive excursions, as well as path stability and range of motion.
The primary analysis will compare baseline mandibular kinematics to post-intervention measurements between the MODJAW-based splint group and the standard splint group.
Measured: Baseline and after 8 weeks of splint use
Secondary outcomes (2)
TMJ pain levels
Patients pain levels will be assessed using a Visual Analog Scale (VAS).
Measured: Baseline and after 8 weeks of splint use
Comfort and satisfaction
Patient comfort and satisfaction will be assessed using a patient-reported questionnaire and 5-point Likert scale.
Measured: Baseline and after 8 weeks of splint use
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted23 Jan 2026
- Study start15 Oct 2025
- Primary completion15 Dec 2025
- Study completion25 Dec 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for BruxismStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Participants are randomly assigned to one of two groups: (1) MODJAW-based patient-specific splint group, or (2) standard occlusal splint group. Each participant follows their assigned intervention for 8 weeks. Outcomes are compared between the groups at baseline and post-intervention.
- Masking
- None (open label)
- Enrolment
- 40 participants (actual)
Sponsor and investigators
- Lead sponsor
- Istanbul University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Dr. Merve Benli, Istanbul University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07364552
- Sponsor's protocol ID
- U-116S697
- Acronym
- MOD-SP
- Status last verified
- Jan 2026
- First submitted
- 12 Jan 2026
- Last updated
- 23 Jan 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided: Individual participant data (IPD) from this study will not be shared. The study involves patient-specific dental records and intraoral imaging that are considered sensitive and personally identifiable. To protect participant privacy and comply with ethical standards, raw data containing personal identifiers will remain confidential and will not be made publicly available. Aggregate or de-identified summary data may be shared upon reasonable request with qualified researchers following approval from the study team and institutional review board.
Study at a glance
From the registry record, last updated by the sponsor on 23 Jan 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Patient-Specific Occlusal Splints Designed Using MODJAW Kinematic Data: A Prospective Clinical Study
- ClinicalTrials.gov ID
- NCT07364552
- Acronym / sponsor ID
- MOD-SP / U-116S697
- Conditions
- Bruxism
- Keywords
- Occlusal splint
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 40 participants (actual)
- Lead sponsor
- Istanbul UniversityUniversity, hospital or other
- Study start
- 15 Oct 2025 (actual)
- Primary completion
- 15 Dec 2025 (actual)
- Study completion
- 25 Dec 2025 (actual)
- First posted
- 23 Jan 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This clinical study is designed to evaluate the effectiveness of patient-specific occlusal splints created using MODJAW, a jaw-tracking device that records 3D mandibular movements. Occlusal splints are commonly used to treat bruxism (teeth grinding) and temporomandibular joint (TMJ) disorders, which can cause jaw pain, headaches, and worn teeth. Traditional splints are made using standard designs that do not consider each patient's unique jaw movements.
In this study, 40 participants with mild-to-moderate bruxism or TMJ dysfunction will be randomly assigned to two groups. One group will receive custom splints designed using MODJAW kinematic data, while the other group will receive standard occlusal splints. Participants will use their assigned splint for 8 weeks.
The study will measure:
Jaw movement patterns using MODJAW
TMJ pain levels
Patient comfort and satisfaction
The main goal is to determine whether MODJAW-based, patient-specific splints provide better jaw function, reduced pain, decreased teeth grinding, and higher patient satisfaction compared to standard splints.
Participants will be monitored throughout the study to ensure safety, comfort, and proper splint use. This study is expected to help dentists design more effective, personalized splints in the future and improve treatment outcomes for people with jaw disorders or bruxism.
Detailed description
Detailed Description:
Background and Rationale:
Bruxism and temporomandibular joint (TMJ) disorders are common conditions that can lead to jaw pain, headaches, tooth wear, and impaired quality of life. Occlusal splints are commonly prescribed to manage these conditions by stabilizing the jaw and distributing occlusal forces. Standard splints, however, are typically fabricated using uniform designs that do not account for the individual jaw movement patterns of each patient. Recent advances in digital dentistry, including the use of jaw-tracking devices such as MODJAW, allow clinicians to capture three-dimensional mandibular kinematics in real time. By using this information, occlusal splints can be designed to match the specific movement patterns of each patient, potentially improving comfort, jaw function, and clinical outcomes.
This study aims to evaluate whether patient-specific occlusal splints designed using MODJAW kinematic data provide superior clinical outcomes compared to standard occlusal splints.
Study Objectives:
To compare mandibular movement patterns between MODJAW-based patient-specific splints and standard occlusal splints.
To evaluate the effect of MODJAW-based splints on bruxism frequency and intensity.
To assess TMJ pain reduction in participants using MODJAW-based splints versus standard splints.
To determine patient satisfaction and comfort with patient-specific versus standard splints.
Study Design:
This is a prospective, randomized, controlled interventional study. Forty participants with mild-to-moderate bruxism or TMJ dysfunction will be randomly assigned to one of two groups:
MODJAW group (n=20): Participants will receive a patient-specific occlusal splint designed based on 3D mandibular kinematic data collected with MODJAW.
Standard splint group (n=20): Participants will receive a conventional occlusal splint fabricated using standard methods.
The study duration for each participant is 8 weeks, during which participants will wear their assigned splints according to instructions and attend follow-up assessments.
Inclusion Criteria:
Age 18-50 years
Diagnosed with mild-to-moderate bruxism or TMJ dysfunction
Willingness and ability to comply with splint use and study visits
Signed informed consent
Exclusion Criteria:
Severe dental loss or existing prosthetic devices interfering with splint placement
Systemic medical conditions affecting jaw function
History of TMJ trauma or surgery
Pregnancy or breastfeeding
Allergy to splint materials
Study Procedures:
Screening and Baseline Assessment:
Clinical examination of dentition and TMJ
Recording baseline jaw movements using MODJAW (for both groups)
Baseline assessment of bruxism frequency, TMJ pain (VAS score), and patient-reported comfort
Splint Fabrication:
MODJAW group: CAD/CAM splints designed using mandibular movement data captured by MODJAW
Standard group: Conventional splints fabricated according to standard occlusal design
Splint Use:
Participants instructed to wear splints nightly (or as directed) for 8 weeks
Weekly check-ins to monitor compliance and comfort
Follow-Up Assessments (Week 4 and Week 8):
Repeat MODJAW recordings to evaluate changes in mandibular movement
Assess TMJ pain, bruxism frequency and intensity
Collect patient satisfaction and comfort scores via 5-point Likert scale
Record any adverse events
Outcome Measures:
Primary Outcome: Changes in mandibular movement patterns as measured by MODJAW
Secondary Outcomes:
Reduction in TMJ pain (VAS score)
Patient-reported satisfaction and comfort
Data Analysis:
Within-group comparisons: Paired t-tests or Wilcoxon signed-rank tests
Between-group comparisons: Mann-Whitney U test
Categorical outcomes: Chi-square or Fisher's exact test
Statistical significance set at p < 0.05
Safety Considerations:
Participants monitored for adverse events related to splint use, including discomfort, tissue irritation, or allergic reactions
Participants may withdraw at any time
All data handled according to confidentiality and privacy guidelines
Significance:
This study will provide evidence on the effectiveness of patient-specific, MODJAW-guided occlusal splints in improving jaw function, reducing bruxism, and increasing patient satisfaction. The results may support the adoption of kinematic data in routine occlusal splint design and contribute to personalized dentistry approaches.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- Participants are randomly assigned to one of two groups: (1) MODJAW-based patient-specific splint group, or (2) standard occlusal splint group. Each participant follows their assigned intervention for 8 weeks. Outcomes are compared between the groups at baseline and post-intervention.
| Arm | Type | Receives |
|---|---|---|
| MODJAW-Based Patient-Specific Splint | Experimental | Device: MODJAW-Based Patient-Specific Occlusal SplintParticipants receive a patient-specific occlusal splint designed using MODJAW 3D mandibular kinematic data. The splint is fabricated via CAD/CAM and worn according to study instructions for 8 weeks. |
| Standard Occlusal Splint | Experimental | Device: Standard Occlusal SplintParticipants receive a conventional occlusal splint fabricated using standard methods. The splint is worn according to study instructions for 8 weeks. |
Who may qualify
- Ages
- 18 to 50 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult
Key inclusion criteria (4 listed)
- Age 18-50 years
- Diagnosed with mild-to-moderate bruxism or temporomandibular joint (TMJ) dysfunction
- Willingness and ability to comply with splint use and study visits
- Signed informed consent
Key exclusion criteria (5 listed)
- Severe dental loss or existing prosthetic devices interfering with splint placement
- Systemic medical conditions affecting jaw function
- History of TMJ trauma or surgery
- Pregnancy or breastfeeding
- Allergy to splint materials
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| MODJAW-Based Patient-Specific Occlusal SplintA custom occlusal splint designed using MODJAW-recorded 3D mandibular movement data. Fabricated via CAD/CAM to fit the patient's unique jaw movements. Worn nightly (or per instructions) for 8 weeks. | Device | MODJAW-Based Patient-Specific Splint |
| Standard Occlusal SplintA conventional occlusal splint made using standard methods without patient-specific mandibular movement data. Worn nightly (or per instructions) for 8 weeks. | Device | Standard Occlusal Splint |
Primary outcome
Improvement in mandibular movement patterns
Time frame: Baseline and after 8 weeks of splint use
Mandibular movements will be recorded using MODJAW 3D jaw-tracking system. Parameters include opening, lateral, and protrusive excursions, as well as path stability and range of motion. The primary analysis will compare baseline mandibular kinematics to post-intervention measurements between the MODJAW-based splint group and the standard splint group.
2 secondary outcomes
TMJ pain levels
Time frame: Baseline and after 8 weeks of splint use
Comfort and satisfaction
Time frame: Baseline and after 8 weeks of splint use
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 23 Jan 2026.
- Participants will wear their assigned splints for 8 weeks, following study instructions. Outcomes will be assessed at baseline and at the end of the 8-week period. Primary outcomes include improvement in mandibular movement patterns measured using MODJAWLink provided by the sponsor.
- Individual participant dataSharing planned: Undecided. Individual participant data (IPD) from this study will not be shared. The study involves patient-specific dental records and intraoral imaging that are considered sensitive and personally identifiable. To protect participant privacy and comply with ethical standards, raw data containing personal identifiers will remain confidential and will not be made publicly available. Aggregate or de-identified summary data may be shared upon reasonable request with qualified researchers following approval from the study team and institutional review board.
Related trials for Bruxism
RecruitingObservational study
Movement of Dental Implants During Osseointegration
Dental Implants, Osseointegration
Enrolling by invitationObservational study
The General Aim is to Implement Clinical Assessment of Overload by Voluntary Bite Force Registration to Enable Future Simple But Precise Risk Assessment to Provide Individualized Treatment Plans.
Dental Implant, Bruxism
Not yet recruiting
Influence Of Different Relaxation Techniques On Stress Level For Patients With Bruxism Using Salivary Biomarkers.
Bruxism, Stress (Psychology)
Not yet recruitingEarly Phase 1
Botulinum Toxin-A for Bruxism Using Digital Occlusal Analysis
Bruxism
RecruitingObservational study
Orofacial Pain and Oral Health-Related Quality of Life in Musicians in German Amateur Orchestras
Orofacial Pain, Sleep Bruxism
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing MODJAW-Based Patient-Specific Occlusal Splint and Standard Occlusal Splint in people with Bruxism, run by Istanbul University at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 23 Jan 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Improvement in mandibular movement patterns (time frame: Baseline and after 8 weeks of splint use). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 Jan 2026; AzTrials last refreshed its copy on 28 Oct 2026.