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Telerehabilitation for TMD

University of Minnesota (UMN) logo

University of Minnesota (UMN)

Status

Completed

Conditions

TMD Headache
Masticatory Myofascial Pain
Temporomandibular Disorder
TMJ Disc Displacement Without Reduction
TMJ Disc Displacement With Reduction
TMJ Arthralgia

Treatments

Other: Telerehabilitation

Study type

Observational

Funder types

Other

Identifiers

NCT05318313
DENT-2022-30141

Details and patient eligibility

About

This study will compare after physical therapy for Temporomandibular Disorders (TMD) performed either in-person or virtually using telerehabilitation. Comparing diagnostic reliability and quality-of-life outcomes in each group will determine (based on a 10% margin) whether delivering physical therapy via telerehabilitation is as good as standard in-person care for these individuals. Long term outcomes including patient satisfaction, cost-effectiveness analysis, and functional status will describe the feasibility of telerehabilitation as a management intervention for this population.

Enrollment

207 patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18-70 years old
  • Referred to PT with ≥1 TMD subtype diagnosis
  • PI has no previous knowledge of the participant's diagnosis
  • Email access
  • Possession of any device that can be positioned for hands-free TR visits (TR group only)
  • Willingness and ability to comply with all study requirements and PT program
  • Able to provide informed consent

Exclusion criteria

  • Non-English speakers

  • Permanent residence outside of the state of Minnesota (TR group only)

  • Women in the last trimester of pregnancy

  • Referred for post-surgical rehabilitation

  • Severe chronic pain as identified by level 4 classification on the GCPS

  • Current diagnosis or existence of the following conditions that can limit response to PT and participation in study activities:

    1. Neuropathic pain
    2. Fibromyalgia and/or generalized widespread pain on both sides of the body in ≥3 areas above and below the waist
    3. Rheumatoid arthritis or juvenile idiopathic arthritis
    4. Dystonia or other movement disorder
    5. Fractures and/or recent jaw or facial trauma
    6. Malignancies
    7. Current substance abuse

Trial design

207 participants in 4 patient groups

Telerehabilitation only
Description:
Participants choose to have all of their physical therapy provided virtually throughout the length of the study
Treatment:
Other: Telerehabilitation
In-person only
Description:
Participants choose to have all of their physical therapy provided in-person throughout the length of the study
Hybrid 1
Description:
The TR PT evaluation and follow-up visits in the initial 6 weeks will be performed via Zoom software and subsequent follow-up visits will switch to in person after 6 weeks
Treatment:
Other: Telerehabilitation
Hybrid 2
Description:
The PT evaluation and follow-up visits in the initial 6 weeks will be performed in person and will switch to TR via Zoom software after 6 weeks
Treatment:
Other: Telerehabilitation

Trial contacts and locations

1

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Central trial contact

Tom Keeler

Data sourced from clinicaltrials.gov

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