OMT vs Exercise in TMD (NCT07534540) | Clinical Trial Compass
CompletedNot Applicable
OMT vs Exercise in TMD
Turkey (Türkiye)50 participantsStarted 2024-04-01
Plain-language summary
The goal of this clinical trial is to evaluate whether different rehabilitation approaches can improve pain, function, and postural control in individuals with temporomandibular disorders (TMD). The study focuses on adults diagnosed with myogenic TMD.
The main questions it aims to answer are:
Does osteopathic manipulative treatment (OMT) reduce pain and improve functional outcomes in individuals with TMD? Does a structured home-based exercise program improve postural control and sensorimotor function in individuals with TMD? Researchers will compare osteopathic manipulative treatment (OMT) and a home-based exercise program to determine their relative effects on pain, function, and postural stability.
Participants will:
Be randomly assigned to either the OMT group or the exercise group Receive the assigned intervention over the study period Undergo assessments before and after treatment, including pain intensity, pressure pain threshold, mandibular movements, cervical range of motion, postural stability, and quality of life
Who can participate
Age range
18 Years – 50 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
TMD Group:
* Diagnosis of temporomandibular disorder (TMD) confirmed by a dentist
* Pain intensity ≥ 3.5 cm on the Visual Analog Scale (VAS)
* Presence of TMD-related pain for at least 3 months
* Aged between 18 and 50 years
* Willingness to participate in the study
Control Group:
* No history or clinical signs of temporomandibular disorder (TMD)
* Aged between 18 and 50 years
* Willingness to participate in the study
Exclusion Criteria:
TMD Group:
* Presence of any condition other than TMD that may affect the assessment outcomes
* Presence of musculoskeletal pain in any other body region
* Any orthopedic or neurological condition that may interfere with assessments
* Diagnosed psychiatric disorder
* Conditions impairing communication or ability to complete assessments
* Illiteracy
* History of orthopedic surgery in any body region
* Presence of systemic pathological conditions such as fractures, rheumatoid arthritis, or suspected malingering
* Receipt of physiotherapy or other treatment targeting the temporomandibular joint or spinal region within the last 6 months
Control Group:
* History of chronic musculoskeletal disorders within the past year
* Any orthopedic or neurological condition that may interfere with assessments
* Diagnosed psychiatric disorder
* Conditions impairing communication or ability to complete assessments
* Illiteracy
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Pain Intensity (Visual Analog Scale, VAS)
Timeframe: Before intervention and immediately after the intervention period