Effects of Soft Tissue Mobilization of Neck Muscles in Individuals With Myogenous Temporomandibular Disorders: Muscle Energy Technique and Strain-counterstrain

NCT ID: NCT04704102

Last Updated: 2021-08-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-01-11

Study Completion Date

2021-06-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This is a prospective case series study.There were 20 individuals with chronic neck pain accompanied by myogenous temporomandibular disorders(mTMD) from Linkou and Taoyuan Chang Gung hospitals, and Chang-Gung university. The purpose of this study was, first, to investigate the effects of muscle energy technique (MET) or strain-counterstrain (SCS) applied on the tender or trigger points of neck muscles on improving pain and pressure pain sensitivity in neck and masticatory muscles, the maximal mouth-opening range of motion, chewing endurance, and head-neck-shoulder posture in patients with chronic neck pain accompanied by mTMD. Second, whether the significant effects could be reached within the four-week intervention duration.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Myogenous Temporomandibular Disorders (mTMD)

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

SEQUENTIAL

Include elements of both longitudinal (three groups) and cross-sectional (four-weeks intervention) research designs
Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Muscle energy technique group

Use one of the muscle energy technique methods -- postisometric relaxation technique(PIR) as the intervention method.

Group Type EXPERIMENTAL

Muscle energy technique (MET)

Intervention Type BEHAVIORAL

A manual therapy technique that uses the gentle muscle contractions of the patient to relax and lengthen muscles and normalize joint motion.

Strain-counterstrain group

Use the Strain-counterstrain technique as the intervention method.

Group Type EXPERIMENTAL

Strain-counterstrain (SCS)

Intervention Type BEHAVIORAL

It's also called the "positional release technique", a manual therapy technique that passively positions the hypertonic (spasmed) muscles and dysfunctional joints in positions of shortened or comfort.

Control group

Use the modified Strain-counterstrain technique as the intervention method.

Group Type SHAM_COMPARATOR

sham SCS

Intervention Type BEHAVIORAL

SCS intervention that position with opposite site limb and direction, and with modified method as consider the easiness of a practitioner to press the tender points

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Muscle energy technique (MET)

A manual therapy technique that uses the gentle muscle contractions of the patient to relax and lengthen muscles and normalize joint motion.

Intervention Type BEHAVIORAL

Strain-counterstrain (SCS)

It's also called the "positional release technique", a manual therapy technique that passively positions the hypertonic (spasmed) muscles and dysfunctional joints in positions of shortened or comfort.

Intervention Type BEHAVIORAL

sham SCS

SCS intervention that position with opposite site limb and direction, and with modified method as consider the easiness of a practitioner to press the tender points

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Aged 20\~65
* Self-report neck pain ≥3 months (pain occurs between superior nuchal line and 1st level of thoracic spine)
* At least one tender point at both Upper trapezius and Sternocleidomastoid muscles
* Diagnosed as mTMD according to the Diagnostic Criteria for Temporomandibular Disorders(DC/TMD)

Exclusion Criteria

* Cognitive deficit
* Malignancy, infection, cervical or orthognathic surgery, acute pain, and history of trauma in craniocervical region
* Neurological problem or cervical radiculopathy/myelopathy
* Cervical instability with positive rotational alar ligament stress test and transverse ligament stress test, jaw dislocation
* Tooth implantation or extraction a week before study
* Vertebrobasilar insufficiency
Minimum Eligible Age

20 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Chang Gung University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Lin Yang-Hua

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Yang-Hua, Lin

Taoyuan District, , Taiwan

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Taiwan

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

2010280044

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Myofascial Release Wıth Hamstring Shortness
NCT07174258 NOT_YET_RECRUITING NA