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Not yet recruiting NCT07226505

Effects of Core Strengthening Exercises for Treating TMD

No phase Interventional Temporomandibular Joint Dysfunction TMD TMJ Internal Derangement Myofascial Pain

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Experimental: Group 1: Core Strengthening, Group 2: Standard TMD PT.
Who it may be relevant to
Registry conditions: Temporomandibular Joint Dysfunction, TMD, TMJ Internal Derangement, Myofascial Pain. Basic parameters: 18 years — 80 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

A Randomized Trial Analyzing the Effects of Core Strengthening Exercises in Physical Therapy for Treating Temporomandibular Joint Dysfunction

Overview

Temporomandibular disorders (TMD) are commonly managed with non-invasive interventions such as manual therapy, therapeutic exercise, relaxation techniques, and patient education. Core strengthening (also known as abdominal strengthening) is a fundamental element of physical therapy that engages deep and superficial trunk musculature to enhance postural control and functional performance. Protocols such as the Shirley Sahrmann progression have demonstrated increased activation of key core stabilizing muscles. Emerging evidence suggests a potential relationship between core stability training and reductions in TMD-related pain, though improvements in functional outcomes remain inconclusive. Biomechanical links between the pelvic floor, spine, and temporomandibular joint further support the rationale for core-focused interventions. Nevertheless, few studies have isolated the effects of core strengthening on TMD symptomatology. This study seeks to determine whether the integration of core stability exercises into TMD management can reduce pain, improve function, and enhance quality of life.

Detailed description

This single-blinded randomized controlled trial will evaluate the effects of core strengthening exercises in addition to standard physical therapy for patients with Temporomandibular Joint Dysfunction (TMD). The study aims to determine whether integrating core stability exercises can reduce TMD-related pain, improve function, and enhance quality of life compared to standard physical therapy alone.

A total of 50 participants, aged 18-70, who have a primary complaint of TMD within the last 30 days and are willing to complete at least six physical therapy visits over a three-month period will be enrolled. Participants must speak English or have access to a verified interpreter and be able to safely participate in exercise.

Participants will be randomly assigned to one of two groups:

Group 1: Core strengthening exercises (Shirley Sahrmann progression) combined with standard TMD physical therapy, including therapeutic exercises, manual interventions, soft tissue mobilization, neuromuscular re-education, and education. Home exercise programs will support adherence.

Group 2: Standard TMD physical therapy alone, including the same therapeutic exercises, manual interventions, soft tissue mobilization, neuromuscular re-education, and education.

Key exclusion criteria include recent TMJ or spinal surgery, recent head/neck trauma or neurologic symptoms, pregnancy, concurrent physical therapy for other movement disorders, low back or pelvic health dysfunction in the past three months, use of dentures, or current chemotherapy/radiation involving the head, neck, pelvis, spine, or hip.

Participants will undergo initial evaluation, intervention sessions, and post-treatment assessment by blinded evaluating therapists to measure pain, function, and core strength outcomes. Safety will be continuously monitored throughout the study.

Interventions

  • Behavioral Experimental: Group 1: Core Strengthening
    Participants perform Shirley Sahrmann core exercises (5 progressive levels maintaining neutral spine and deep core activation), possibly adding upper extremity movements. Standard TMD PT includes jaw exercises, manual therapy, soft tissue mobilization, neuromuscular re-education, and patient education. A home exercise program (\~20 min/day) is provided with printed and video instructions.
  • Behavioral Group 2: Standard TMD PT
    Participants receive standard TMD PT including jaw exercises (Rocabado 6x6), manual therapy for TMJ and cervical spine, soft tissue mobilization, neuromuscular re-education to improve jaw mechanics, and education on jaw positioning, diet/chewing modifications, and parafunctional habits. A home exercise program is provided as part of treatment.

Primary outcome measures

  • TMD Pain (e.g., Visual Analog Scale/Numeric Pain Rating) [Time frame: Baseline and post-intervention (6 PT sessions), assessed up to 6 weeks]
Secondary outcome measures (3)
  • Neck Disability Index (NDI) [Time frame: Baseline and post-intervention (6 PT sessions), assessed up to 6 weeks]
  • Compliance with Home Exercise Program (HEP) [Time frame: Throughout the 6-week intervention period (daily tracking, summarized at post-intervention)]
  • Functional Measures from TMJ Scale [Time frame: Baseline and post-intervention (6 PT sessions), assessed up to 6 weeks]

Eligibility criteria

Who Can Participate (Inclusion Criteria):

Adults between 18 and 70 years old.

Have had jaw pain or problems with the jaw joint (TMD) in the last 30 days.

Able and willing to attend at least six physical therapy sessions over three months.

Speak English or have access to a qualified interpreter.

Able to safely do physical exercises.

Who Cannot Participate (Exclusion Criteria):

Recently had surgery on the jaw, teeth, or spine (within the last 3 months).

Recently had head or neck injuries or certain neurological problems (such as dizziness, double vision, trouble swallowing, or sudden falls).

Are pregnant or become pregnant during the study.

Currently doing physical therapy for other movement problems that could affect the study.

Have had lower back or pelvic health issues in the last 3 months.

Currently receiving chemotherapy or radiation for cancer in the head, neck, pelvis, spine, or hip.

Wear dentures or cannot safely perform exercises.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Treatment

Study locations

United States · 1 center
  • Loyola University Medical Center — Maywood

Identifiers

NCT: NCT07226505 · 219911

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗