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Clinical Trials/NCT04294602
NCT04294602
Completed
Not Applicable

Efficacy Of Different Types Of Physiotherapy Approaches In Temporomandibular Disorders

Bitlis Eren University1 site in 1 country59 target enrollmentMay 15, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Temporomandibular Disorder
Sponsor
Bitlis Eren University
Enrollment
59
Locations
1
Primary Endpoint
Pain Severity Assessment
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The aim of this study is to investigate the efficacy of different types of physiotherapy approaches in cases with cervical myofascial painful TMD.

Detailed Description

59 persons with TMD diagnosed by the dentist and with cervical myofascial pain, aged 18-30 years will be randomly allocated, 3 groups. The participants were randomly allocated only exercise group (EG) (n=20), low-level laser therapy plus exercise group (LLLT) (n=17) and manual pressure release plus exercise group (MPR) (n=22). The cases were evaluated and treated by the same physiotherapist for 4 weeks (12 sessions). Pain, pain pressure threshold, temporomandibular joint (TMJ) mobility and disability, forward head posture, head rotation, neck disability, psychological status and quality of life were evaluated. Evaluations were repeated before and after treatment.

Registry
clinicaltrials.gov
Start Date
May 15, 2017
End Date
May 10, 2018
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Bitlis Eren University
Responsible Party
Principal Investigator
Principal Investigator

Abdurrahman Tanhan

research assistant

Bitlis Eren University

Eligibility Criteria

Inclusion Criteria

  • Cases who have 3 or more symptoms related to TMJ problems
  • cases who have trigger points in cervical and masticatory muscles
  • cases who TMD detected by the dentist,
  • being between the ages of 18-30,
  • volunteer to participate in the study

Exclusion Criteria

  • Patients with a positive history of trauma in the face and neck area and neurological disorders
  • patients undergoing TMJ or cervical region surgery in the last 3 months,
  • patients who used dental orthotics within 1 month,
  • patients who have TMJ instability,
  • patients who have cervical and upper thoracic region,
  • patients who have active infection and chronic pain, such as trigeminal neuralgia

Outcomes

Primary Outcomes

Pain Severity Assessment

Time Frame: Change from baseline TMJ pain and intensity of head pain, TMJ noise and jaw locking score at week 4.

To evaluate the general pain severity of the patients, the Visual Analog Scale (VAS), which is the Visual Pain Scale of Turkish, was used. Patients were asked to mark their general pain separately on a 10 cm scale. According to this, "0" indicates that there is no pain, and "10" indicates the most severe pain. The distance between the marked point and the beginning of the line was recorded in centimeters

Jaw Movements Assessment

Time Frame: Change from baseline MMO and lateral deviation score at week 4.

Maximum mouth opening (MMO) and lateral deviation were measured with a caliper.

Quality of Life Assesment

Time Frame: Change from baseline quality of life score at week 4

Short Form-36 questionnaire contains the physical and mental component, which is evaluated, is close to 100, indicating an increase in health-related quality of life. The means SF-36 score ranging from 0 (worst) to 100 (best).

Temporomandibular Disorder Severity

Time Frame: Change from baseline temporomandibular disorder severity score at week 4

The TMD severity in participation is defined by the Craniomandibular Index (CMI) which was developed to provide a standardized measure to the severity of problems in mandibular movement, muscle, and joint tenderness and TMJ noise for use in epidemiological and clinical outcome studies. The instrument was designed to have clearly defined objective criteria, simple clinical methods, and ease in scoring; it is divided into the Palpation Index (PI) and the Dysfunction Index (DI). The means of the subscales were averaged to produce a CMI score ranging from 0 (best) to 1 (worst)

Pressure Pain Threshold Assessment

Time Frame: Change from baseline pressure pain threshold score in neck and mastication muscles at week 4.

Pressure Pain Threshold (PPT) of an individual's mastication and cervical muscle was measured with an algometer (JTECH Medical Industries, CommanderTMAlgometer), and the applied pressure was increased to 1 cm2/ kg per second. PPT measurements were repeated three times and the average was used for analysis in every participant.

Neck Movements Assessment

Time Frame: Change from baseline cervical rotations and craniovertebral angle score at week 4.

Cervical rotations and the craniovertebral angle between C7 and tragus were measured by a goniometer.

Secondary Outcomes

  • Psychological Status Assesment(Change from baseline psychological status score at week 4.)
  • Neck Disability Assesment(Change from baseline neck disability score at week 4.)

Study Sites (1)

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