Actively Recruiting

Phase Not Applicable
Age: 18Years - 55Years
All Genders
NCT06602375

The Effect of Manual Physical Therapy and Exercise in Addition to Routine Dental Care in Individuals With Temporomandibular Disorders

Led by Brooke Army Medical Center · Updated on 2025-02-05

60

Participants Needed

1

Research Sites

93 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this randomized clinical trial among US military active-duty service-members with temporomandibular disorders (TMD) is to determine whether standard care plus 6-weeks of tailored, individualized physical therapy (PT) treatment provides greater benefit than standard care alone in patient-reported outcomes, and maximal mouth opening. The aims of the study are to compare outcomes in individuals with TMD that receive standard care treatment versus standard care plus PT interventions at 0-, 6-, and 12-weeks. The investigators anticipate that subjects in the standard care plus PT group will exhibit improved patient-reported outcomes, and maximal mouth opening compared to those who received standard care alone. Additionally, the investigators will compare the amount and type of healthcare utilization between the two groups (Standard Care and Standard Care + PT) in the 12-month period following enrollment in the study. All participants will be managed by their primary dental provider and receive care as deemed appropriate by their provider. All participants will complete patient-reported outcome measures and have their jaw motion measured. Those randomized to the standard care plus PT group will also receive a tailored PT evaluation followed by an individualized plan of care two times per week for up to six weeks.

CONDITIONS

Official Title

The Effect of Manual Physical Therapy and Exercise in Addition to Routine Dental Care in Individuals With Temporomandibular Disorders

Who Can Participate

Age: 18Years - 55Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Active-Duty Service Members
  • Complaint of TMD symptoms
  • Must be able to be followed for twelve weeks after consent
  • TMD Screener score 63 3 45
Not Eligible

You will not qualify if you...

  • Actively in a Trainee status
  • Utilized oral device in past 6 months
  • Facial injection therapy in the prior 6 months
  • Facial surgery in the preceding 6 months
  • Serious spinal pathology (acute fracture, active cancer, instability)
  • Diagnosed neurological or rheumatological disease
  • Currently under litigation related to temporomandibular or cervical spine pain(s)
  • Currently undergoing Medical Evaluation Board (MEB)
  • Retiring or separating from the military within a year

AI-Screening

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Trial Site Locations

Total: 1 location

1

Brooke Army Medical Center

Fort Sam Houston, Texas, United States, 78234

Actively Recruiting

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Research Team

M

Mason A Frank, DPT

CONTACT

B

Benjamin R Hando, PhD, DPT

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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