Effects of Orofascial Myofunctional Therapy and Cervical Stabilization Exercises on Temporomandibular Dysfunction

NCT ID
NCT07828587
Registry status
Not yet recruiting
Study type
Interventional
Phase
Not applicable
Sponsor
Lahore University of Biological and Applied Sciences
Conditions
Disc Displacement, Temporo-mandibular Dysfunction, Temporomandibular Disorders (TMDs)

Overview

ClinicalTrials.gov lists this study as Not yet recruiting.

Official title: Effects of Orofascial Myofunctional Therapy and Cervical Stabilization Exercises on Jaw Pain, Range of Motion, Occlusal Load and Functional Limitation in Patients With Temporomandibular Dysfunction

Enrollment: 80 participants (Estimated).

What is being studied

  • Intervention: Aftercare
  • Other: cervical stabilization exercises
  • Intervention: Continuity of Patient Care
  • Intervention: Dentistry
  • Intervention: Myofunctional Therapy
  • Other: orofacial myofunctional therapy
  • Intervention: Patient Care
  • Intervention: Physical Therapy Modalities
  • Intervention: Rehabilitation
  • Intervention: Rehabilitation of Speech and Language Disorders
  • Intervention: Therapeutics

Who may be eligible

Ages
18 Years to 35 Years
Sex
All
Healthy volunteers accepted
No

ClinicalTrials.gov lists the following eligibility criteria.

Inclusion Criteria: * All genders * Aged between 18-35 years * Intra-articular, anterior disc displacement with reduction of TMJ, based on RDC/TMD criteria * Axis-I, group II - Disc displacement with reduction * Clinically diagnosed patients with Anterior Disc Displacement with Reduction (ADDR) from Maxillo-facial surgery department * Diagnostic screening will be conducted using a cluster of clinical tests, including jaw compression, traction, and translation maneuvers, static and dynamic resistance testing, and clenching provocation * A positive diagnosis will be established when five of the six tests demonstrate positive findings * All patients and subjects had permanent dentition; none had dental pain or periodontal problems, neurological or cognitive deficit * Symptoms persist for ≥ 3 months * Pain should not be less than 4/10 on NPRS * Maximum mouth opening ≥ 40mm * Maximum relative occlusal load (50% rule) Exclusion Criteria: * Severe systemic conditions affecting muscles or joints (e.g., rheumatoid arthritis, fibromyalgia, generalized joint hypermobility, neuromuscular disorders). * Any psychiatric or neurological disorders interfering with adherence (e.g., uncontrolled epilepsy, major psychiatric illness such as anxiety, stress, or depression). * Previous TMJ surgery, arthroscopy, arthrocentesis, or injection therapy in the past 6 months. * Ongoing dental appliance therapy (splints/braces) unless stabilized for at least 3 months. * Suspected neoplasm, infection, or fracture in the craniofacial region. * Progressive neurological deficits (e.g., facial numbness, motor weakness). * Severe or constant night pain not relieved by rest (which may indicate pathology beyond disc displacement with reduction). * Insomnia or disturbed sleep quality.

Study locations

1 study location is listed.

Site recruitment status is not specified in the registry data for these locations.

Countries: Pakistan

  • Punjab Province, Pakistan: 1

Sample of listed locations

  • Dr. Umber Nawaz — Lahore, Punjab Province, 54770, Pakistan — Site recruitment status not specified in the registry data

Study details

Start date
September 15, 2026
Primary completion date
December 15, 2026
Completion date
February 15, 2027
First posted
September 18, 2026

Source and update information

Source
ClinicalTrials.gov
NCT ID
NCT07828587
Registry last updated
September 18, 2026
QualifiedStudies registry data refreshed
October 5, 2026
QualifiedStudies record fetched
October 5, 2026

View NCT07828587 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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