- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04755621
The Effect Of Core Stability Training In Temporomandibular Disorders
February 12, 2021 updated by: Emre Serdar Atalay, Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey
The Effect Of Core Stability Training on Pain, Function and Quality of Life in Individuals With Temporomandibular Disorders
This study is to investigate the effect of Core stability training on pain, function, quality of life, sleep quality, body posture, foot posture, oral habits and kinesiophobia in individuals with temporomandibular disorder.
Materials and Methods: The study included 40 people over the age of 18, who were diagnosed with temporomandibular disorder from the dentist.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
40
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
-
-
Uskudar
-
İ̇stanbul, Uskudar, Turkey, 34668
- University and Health Sciences Physical Therapy and Rehabilitation
-
-
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
18 years to 55 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Male and female patients aged 18-55, diagnosed with temporomandibular disease by a dentist
Exclusion Criteria:
- Having received another treatment for TMR other than the use of night plate in the last 6 months
- Having a disease that can cause facial pain such as sinusitis, migraine, tension headache, trigeminal neuralgia
- Skeletal system fractures
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: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Control Group
|
Exercises for Temporomandibular Disorders
|
|
Experimental: Core stability Group
|
Core stability exercises
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Posture
Time Frame: 6 weeks
|
New York Posture Scale
|
6 weeks
|
|
Sleep Quality
Time Frame: 6 weeks
|
Pittsburg Sleep Quality Index
|
6 weeks
|
|
Kinesiophobia
Time Frame: 6 weeks
|
Tampa Scale for Kinesiophobia for Temporomandibular Disorders (TSK-TMD)
|
6 weeks
|
|
Oral Habits
Time Frame: 6 weeks
|
Oral Behavior Checklist
|
6 weeks
|
|
Jaw Function
Time Frame: 6 weeks
|
Jaw Functional Limitation Scale-20
|
6 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Foot Posture
Time Frame: 6 weeks
|
Foot Posture Index-6
|
6 weeks
|
|
Graded Pain
Time Frame: 6 weeks
|
Graded Chronic Pain Scale
|
6 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Director: Emre Serdar Atalay, PhD, University of Health Sciences, Physical Therapy and Rehabilitation
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)
April 1, 2019
Primary Completion (Actual)
August 1, 2019
Study Completion (Actual)
September 1, 2019
Study Registration Dates
First Submitted
January 28, 2021
First Submitted That Met QC Criteria
February 12, 2021
First Posted (Actual)
February 16, 2021
Study Record Updates
Last Update Posted (Actual)
February 16, 2021
Last Update Submitted That Met QC Criteria
February 12, 2021
Last Verified
February 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 46418926-050.01.04
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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