- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05709340
PNF Exercises on Treatment of Temporomandibular Dysfunction
April 17, 2023 updated by: Marwa Shafiek Mustafa Saleh, Cairo University
Efficacy of PNF Exercises on Treatment of Temporomandibular Dysfunction in Patients With Forward Head Posture: A Double-blind, Randomized, Controlled Trial
Temporomandibular joint dysfunction (TMJD) is an important health problem that occurs approximately in 22 to 35 percent of adults, different physiotherapy methods are reported as treatment options for management of TMJD.
Although that, there is no previous studies about the efficacy of PNF exercises in treatment of TMJD in patients with forward head posture.
So, the purpose of the present double-blind, randomized, controlled trial is to investigate the efficacy of PNF exercises in treatment of TMJD in patients with forward head posture.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
24
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Giza, Egypt
- marwa S saleh
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years to 40 years (Adult)
Accepts Healthy Volunteers
No
Description
Inclusion criteria:
- Patients of both genders of age between 20-40 years
- having symptoms of TMD for at least six weeks duration established by an expert physician or orthopaedician
- having forward head posture with CVA < 53
- pain over TMJ between 3 to 6 on NPRS
- mouth opening < 25mm.
Exclusion criteria:
Patients will be excluded if they exhibited any of the following criteria:
- TMJ fracture undergone any surgical procedure for TMJ
- Fracture surrounding TMJ
- Dislocation or subluxation of TMJ
- systemic generalized joint diseases, such as rheumatoid arthritis, and osteoporosis, congenital diseases, or facial paralysis
- recently any dental treatment is taken or surgery over TMJ
- hematological cervical disorders which may affect the jaw
- Neurological deficits e.g. Bells palsy, Trigeminal neuralgia.
- Recent infections (within the last six months) affecting the head and neck e.g. bone infections, meningitis, encephalitis, malaria, ear infection
- Participants who were using any functional appliances e.g. dentures, braces, bite appliances which had been adjusted or fitted in the last 12 weeks prior to the commencement of this study
- DDwR, DDwoR
- Patients were excluded from the study if they were receiving any other form of treatment for their TMJ dysfunction.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
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Active Comparator: control group
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Experimental: study group
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PNF exercises will be done for Masseter, Temporalis, Lateral pterygoid and medial pterygoid muscles.
Each contraction will be held for 10 seconds, and each stretch (relaxation phase) will be allowed to continue as long as the muscle tension continued to give away.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Pressure Pain Threshold
Time Frame: change from base line at 6 weeks.
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A pressure algometer will be used for the objective measurement of the PPT.
The algometer was pressed on the masseter, temporalis muscles until the patient feel pain.
The unit of measurement will be in kg/cm2, and three measurements will be taken every 30 seconds.
The average of the three consecutive measurements will be taken as the final value.
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change from base line at 6 weeks.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
ROM assessment
Time Frame: change from base line at 6 weeks.
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A caliper will be used to measure mandibular depression, protrusion and lateral deviation.
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change from base line at 6 weeks.
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Temporomandibular Disorder Disability Questionnaire
Time Frame: change from base line at 6 weeks.
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This questionnaire consists of the following:
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change from base line at 6 weeks.
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Numerical Rating Scale (NRS)
Time Frame: change from baseline at 6 weeks.
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The patient will be asked to indicate a number between 0 and 100 on a horizontal line, that best described his/her perceived level of pain intensity when it is at its worst and when it is at is least.
The average of these two totals indicates the average pain experienced by the patient as a percentage.
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change from baseline at 6 weeks.
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 25, 2023
Primary Completion (Actual)
March 25, 2023
Study Completion (Actual)
April 15, 2023
Study Registration Dates
First Submitted
January 21, 2023
First Submitted That Met QC Criteria
January 21, 2023
First Posted (Actual)
February 2, 2023
Study Record Updates
Last Update Posted (Actual)
April 18, 2023
Last Update Submitted That Met QC Criteria
April 17, 2023
Last Verified
April 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- PNF exercises for TMJ
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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