Actively Recruiting
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
Eligibility Criteria
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
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
AI-Powered 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
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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