Conservative Treatment of Patients With Temporomandibular Disorders

Not Applicable

Completed

Conditions: Temporomandibular Disorders

Interventions: Other: Sham AMCT
Device: Chiropractic w/Activator & Self Care
Device: Dental Care & Self Care
Other: Self-Care Only Group

Registration Number: NCT01021306

Lead Sponsor: Palmer College of Chiropractic

Brief Summary: At any given time, 10 million Americans suffer from temporomandibular disorders (TMD), with a lifetime prevalence of 45% and costs for direct care exceeding $2 billion/year. Little evidence exists regarding the efficacy of specific conservative interventions used to treat TMD and currently there is no "gold standard" of care that is widely accepted by the dental or medical community. This study is a prospective, randomized 4 arm parallel observer-masked pilot study comparing: 1) Activator Methods Chiropractic Technique (AMCT), 2) a conservative dental approach with reversible interocclusal splint therapy, 3) a sham AMCT, and 4) a self-care only group, which includes a standard checklist of self-care jaw relaxation techniques, for a total of 80 patients with chronic myofascial TMD.

Detailed Description: All patients will be offered the self-care checklist of homecare approaches at baseline. Patients will be treated for two months with follow up at 3 and 6 months after enrollment. The primary outcome measure will be an 11 point Numerical Rating Scale for average TMD pain during the past week. Secondary outcomes will include the Oral Health Impact Profile (OHIP-14), believability of the sham AMCT compared to active AMCT, expectations of and satisfaction with care, medication use, bothersomeness of symptoms and health care utilization. Our project is a collaborative effort between the Palmer Center for Chiropractic Research (PCCR) and the University of Iowa (UI) through the College of Dentistry and the General Clinical Research Center (GCRC) Oral and Craniofacial Unit. The PCCR Clinic and Data Core will serve as the data coordinating center and will develop a web-based data collection system for this project. Patient eligibility will be assessed by dental examiners at the UI College of Dentistry using the Research Diagnostic Criteria for Temporomandibular Disorders to diagnose chronic, Axis I myofascial TMD. Dental care will be provided by a dentist at UI GCRC and chiropractic care will be provided by a private practitioner in close proximity to UI. The aims of this project are to assess the feasibility of conducting a full-scale randomized clinical trial to evaluate the effectiveness of AMCT for patients with chronic myofascial TMD; determine the most appropriate control group(s) for a full-scale randomized controlled trial; and to estimate the sample size needed for an adequately-powered trial and the recruitment period that would be required. In general, there is a lack of evidence for the efficacy of non-surgical treatment for patients with TMD, including chiropractic interventions. If the beneficial effects of the AMCT are supported in this pilot study, the logistical information gained will allow us to plan a full scale trial for patients suffering pain and disability due to TMD. It is anticipated that such a trial will allow clinicians to make more informed recommendations for treatment of patients with TMD. At the conclusion of this project, we will be well-positioned to prepare an R01 level grant application.

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 80

Inclusion Criteria

Age 21 years or older
TMD symptoms for at least 6 months
Must have 7-8 teeth per dental arch that are in occlusion (can be restored teeth or dental implants with crowns or fixed dental bridgework)
Typical TMD pain during the past week > = 3 on an 11 point Numerical Rating Scale
RDC/TMD Axis I diagnosis of myofascial pain (Group Ia or Ib) with or without a concurrent diagnosis of arthralgia (Group IIIa) or disk displacement with reduction (Group IIa)
Stable prescription medication plan: no changes in prescription medication for pain during the past month

Exclusion Criteria

Current or pending litigation for a personal injury case, worker's compensation, or disability
Participants with unstable periodontitis and/or a dental condition with untreated disease (e.g., caries). Participants may elect to have her/his dental care provided to stabilize their dental condition prior to randomization.
Subjects with Canine Class II malocclusion that would prohibit fabrication of RIST appliance
Cases that need further diagnostic procedures to rule in or rule out the condition (i.e., MRI or CT scan)
Systemic arthritis or other serious medical condition necessitating maximum daily dosing of COX-2 inhibitor or NSAIDs, (All NSAID use will be recorded in the daily diary as a part of the Self-Care data recording).
Participants presenting with complete dentures
Any treatment for TMD during the previous month, except for non-prescription medications or a stable prescription medication regimen for TMD.
Inability to read or verbally comprehend English
Unwillingness to be enrolled in any of the four intervention groups.
Unwillingness to postpone other forms of treatment for TMD during the two month active care phase (except for non-prescription medications or continuation of a stable prescription medication regimen).
Unwillingness to postpone any chiropractic care during the two month active care phase.
Intention to move from the area during the next seven months
Ever had active chiropractor care for TMD pain
Drug or alcohol abuse
Pregnant or planning to be pregnant during next seven months
MVA or other trauma in the last six months
Facial pain/TMD not worst pain
General poor health
Extensive dental work in past 6 months including orthodontics
Serious co-morbid conditions, including: Lupus Erythematosus, Sjogren's Syndrome, Multiple Sclerosis, Symptomatic Trigeminal Neuralgia (tic/tic douloureux) or any other neuralgia of the face, Thyroid problem not controlled by medication, Uncontrolled diabetes, Rheumatoid arthritis, Fibromyalgia, Polymyalgia Rheumatic, Giant Cell Arteritis, Psoriatic Arthritis, Reiters Syndrome, Bechets Syndrome, Crohn's Disease, Ulcerative Colitis, Parkinson's Disease, Tardive Dyskinesia, Active seizure disorder, Stroke with head and neck symptoms, Addison's Disease, Cushing's Disease
Have had or ever had any type of head or neck surgery within the last 6 months
Have had or ever had radiation treatment to the head and/or neck
Have had or ever had surgery of your jaw joints, not including arthroscopic surgery
Have had or ever had Herpes Zoster or shingles in the face

Study & Design

Study Type: INTERVENTIONAL

Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Sham AMCT & Self Care	Sham AMCT	This protocol will attempt to follow all of the procedures of the actual AMCT protocol except no thrust will be delivered. Self-care only participants successfully completing the 6 month assessment will be given the option for RIST or AMCT for one month.
Chiropractic w/Activator & Self Care	Chiropractic w/Activator & Self Care	This technique uses a hand held instrument to deliver a quick, shallow thrust in a well defined manner.
Dental Care & Self Care	Dental Care & Self Care	Intraoral splints are removable orthopedic appliances fabricated of hard acrylic resin positioned between the remaining teeth of the patient. They are designed in theory to support the function of the TMJ and relieve associated pain. Stabilization splints are believed to function by stabilizing the intracapsular structure of the TMJ, reducing activity of masticatory muscles, distributing occlusal forces, and reducing bruxism (teeth grinding).
Self-care only group	Self-Care Only Group	All patients will be offered the self-care checklist of homecare approaches at baseline. Self-care only participants successfully completing the 6 months assessment will be given the option for RIST or AMCT for one month.

Primary Outcome Measures

Name	Time	Method
Patient-Rated TMD Pain, an 11 Point Numerical Rating Scale (NRS)	2 months	The Numerical Rating Scale ranges from 0 (no pain) to 10 (pain as bad as it can be).

Secondary Outcome Measures

Name	Time	Method
Bothersomeness of Symptoms	2 months	Possible ratings range from 1 (not at all bothersome) to 5 (extremely bothersome)
Oral Health Impact Profile (OHIP-14)	2 months	The OHIP-14 contains 2 questions about each of 7 dimensions (14 items), indicating how often the participant had experienced each difficulty in the previous month; possible responses range from 0 (never) to 4 (very often). The OHIP score was obtained by summing the 14 ratings.

Trial Locations

Locations (3): Palmer College of Chirpractic
🇺🇸
Davenport, Iowa, United States
Schaeffer Chiropractic
🇺🇸
Coralville, Iowa, United States
University of Iowa College of Dentistry
🇺🇸
Iowa City, Iowa, United States