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RecruitingNCT07203456Updated Oct 2, 2025

Testing Educational Modalities for Temporomandibular Disorders Curriculum

An interventional study of Virtual Patient Based Learning (VPBL) and Clinical exposure to patients with TMD in Confidence and Diagnostic Ability, sponsored by Midwestern University. Recruiting at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-10-02.

Sponsored by Midwestern University · Not applicable, Interventional, and Other

From the registry’s dates

  • Started Jun 2025; still recruiting 1 year 4 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
90
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
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Study summary

This study is done to assess the change in confidence level, knowledge, and diagnostic ability in TMD-related aspects through the exposure to a Virtual Patient-Based Learning (VPBL) platform featuring temporomandibular disorder (TMD) cases among 3rd and 4th year predoctoral dental students at a larger predoctoral school.

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Conditions studied

  • Confidence
  • Diagnostic Ability
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In context

Lead sponsor

Midwestern University is the lead sponsor of 20 studies on the registry; 5 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Third or Fourth year dental students at the College of Dental Medicine at Midwestern University (Illinois)

Exclusion criteria

Exclusion Criteria:

  • Dental students not enrolled at the third and/or fourth year of the College of Dental Medicine at Midwestern University (Illinois)
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Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
90 participants (estimated)

Study arms

  • Active comparator
    Clinical exposure to patients with TMD

    Participants will be exposed to clinical patients with TMD

    Other: Clinical exposure to patients with TMD

  • Active comparator
    Clinical exposure to patients with TMD and virtual patient based learning (VPBL)

    Participants will be exposed to clinical patients with TMD and to the corresponding virtual patient with the same TMD diagnosis featured on the VPBL

    Other: Clinical exposure to TMD + VPBL

  • Experimental
    Virtual Patient Based Learning (VPBL)

    Participants will be exposed to review virtual patients featured on the VPBL

    Other: Virtual Patient Based Learning (VPBL)

Interventions

  • OtherVirtual Patient Based Learning (VPBL)

    A digital platform featuring 20 virtual patients has been built to increase predoctoral student clinical exposure to patients with TMD signs and symptoms

  • OtherClinical exposure to patients with TMD

    Participants in this arm will be exposed to patients with TMD signs and symptoms, to the history taking, interview, clinical examination, diagnostic process, and treatment plan under the supervision of an orofacial pain specialist

  • OtherClinical exposure to TMD + VPBL

    Participants will be exposed to patients with TMD signs and symptoms (including history taking, interview, clinical exam, diagnostic process, and treatment plan) under the supervision of an orofacial pain specialist, and then will be exposed to the corresponding TMD patient on the VPBL, featuring virtual patients with TMD

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What researchers measure

Primary outcomes

  1. Self-perceived Confidence Level

    Change in confidence level between baseline and after the educational intervention. The self-perceived confidence level will be measured with a 12-item confidence level scale (previously developed and validated by the research group), where answer options range from 0 to 10 on a numerical rating scale (with 0 = "not confident at all" and 10 = "extremely confident"). The 12 items refer to TMD-related skills, including but not limited to providing a treatment plan for patients with TMD, screening of TMD patients, education on the TMD condition, performing diagnostic injections, referring to healthcare providers, among others.

    Time frame: Immediately after the educational intervention

Secondary outcomes

  1. Diagnostic ability in diagnosing TMD cases

    Change in diagnostic ability in TMD. The diagnostic ability in TMD will be assessed by providing case scenarios featuring signs and symptoms of various TMD conditions. The user will be asked to indicate the TMD diagnosis of the described case. Diagnostic ability will be evaluated based on the accuracy of identifying the correct TMD condition based on the Diagnostic Criteria for TMD (DC/TMD). Answers will be given a score of 1 in case of accurate diagnosis and 0 in case of inaccurate diagnosis.

    Time frame: Immediately after the educational intervention

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Study locations

1 of 1 sites recruiting
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References and documents

Publications

  • Sangalli L, Manning E, Abdykarimova A, Gao O, Lok B, Hawkins J, Miller CS. Integrating virtual patient-based learning into temporomandibular disorder education improves educational and behavioral outcomes. BMC Med Educ. 2026 May 9;26(1):1063. doi: 10.1186/s12909-026-09388-0. PubMed 42106674 ↗

Individual participant data

Plan to share: No

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 2, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07203456
Lead sponsor
Midwestern University
Responsible party
Sponsor
First posted
Oct 2, 2025
Start date
Jun 13, 2025
Primary completion
Oct 1, 2026 (estimated)
Completion
Oct 1, 2026 (estimated)
Last update
Oct 2, 2025

Study contacts

Linda Sangalli, DDS, MS, PhD
Contact
lsanga@midwestern.edu
630-515-4617

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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