Effectiveness of the Fascial Distortion Model on the Cervical Spine in Individuals With Temporomandibular Disorder
Effectiveness of Manual Therapy Based on the Fascial Distortion Model on the Cervical Spine in Individuals With Temporomandibular Disorder
1 other identifier
interventional
51
1 country
2
Brief Summary
The goal of this randomized clinical trial is to investigate the effectiveness of Manual Therapy Based on the Fascial Distortion Model (FDM) on the cervical spine by comparing it with Core Stabilization Training (CST) or Control in individuals with temporomandibular disorders. The main questions it aims to answer are: Is the effectiveness of the addition of FDM-based Manual Therapy to conventional therapy different from the addition of CST or control? Is the effectiveness of the addition of CST to conventional therapy different from the addition of FDM or control? All participants in the intervention groups will be given eight-week conventional therapy (Rocabado Exercises and Patient Education) in addition to FDM-based Manual Therapy or CST. Participants in the control group will not be given any therapy during the study. Neck pain intensity, hand grip strength, head posture, cervical muscle performance, cervical range of motion (function), disability, and quality of life will be assessed.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Dec 2023
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 17, 2023
CompletedStudy Start
First participant enrolled
December 17, 2023
CompletedFirst Posted
Study publicly available on registry
January 2, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 30, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
January 2, 2025
CompletedMarch 13, 2025
July 1, 2024
3 months
December 17, 2023
March 11, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (13)
Eye-Tragus-Horizontal Angle on lateral photography of head posture
The angle between the line connecting the midpoint of the lateral corner of the eye to the tragus of ear and the horizontal line emerging from the tragus level. It refers to the cranial rotation angle
From enrollment to the end of treatment at 8 weeks
Pogonion-Tragus-C7 Angle on lateral photography of head posture
The angle between the line connecting the pogonion (the most protruding point on the front of the mandible) to the tragus and the line connecting the tragus to the C7 vertebra
From enrollment to the end of treatment at 8 weeks
Tragus-C7-Horizontal Angle on lateral photography of head posture
The angle between the line connecting the tragus to the C7 vertebra and the horizontal line emerging from the C7 vertebra level. It refers to the neck inclination angle
From enrollment to the end of treatment at 8 weeks
Tragus-C7-Shoulder Angle on lateral photography of head posture
The angle between the line connecting the acromion to the C7 vertebra and the line connecting the C7 vertebra to the tragus. It refers to the sum of the tragus-C7-horizontal angle and the shoulder-C7-horizontal angle; Shoulder-C7-Horizontal Angle (5): The angle between the line connecting the acromion to the C7 vertebra and the horizontal line emerging from the C7 vertebra level. It refers to the angle of the shoulder.
From enrollment to the end of treatment at 8 weeks
Shoulder-C7-Horizontal Angle on lateral photography of head posture
The angle between the line connecting the acromion to the C7 vertebra and the horizontal line emerging from the C7 vertebra level. It refers to the angle of the shoulder.
From enrollment to the end of treatment at 8 weeks
Disability based on Neck Disability Index
Neck Disability Index. Minimum and maximum values are 0 and 5 points, respectively. Higher scores mean a worse outcome.
From enrollment to the end of treatment at 8 weeks
Quality of Life based on Cognitive Exercise Therapy Approach-Biopsychosocial Questionnaire
Cognitive Exercise Therapy Approach-Biopsychosocial Questionnaire. Minimum and maximum values are 0 and 4 points, respectively. Higher scores mean a worse outcome.
From enrollment to the end of treatment at 8 weeks
Chronic neck pain intensity
Graded Chronic Pain Scale (Revised). Scoring: Grade 1=mild, Grade 2=bothersome, Grade 3=high impact chronic pain. Higher scores mean a worse outcome.
Baseline, 2nd week, 4th week, 6th week and 8th week
Neck pain intensity at last seven days based on Short-Form McGill Pain Questionnaire
Short-Form McGill Pain Questionnaire. Minimum and maximum values are 0 and 3 points, respectively. Higher scores mean a worse outcome.
Baseline, 2nd week, 4th week, 6th week and 8th week
Present neck pain intensity
Visual Analog Scale. Minimum and maximum values are 0 and 10 cm, respectively. Higher scores mean a worse outcome.
Baseline, 2nd week, 4th week, 6th week and 8th week
Present neck pain intensity (ordinal)
Present pain intensity scale of McGill Pain Questionnaire. Minimum and maximum values are 0 and 5 points, respectively. Higher scores mean a worse outcome.
Baseline, 2nd week, 4th week, 6th week and 8th week
Neck pain intensity at last seven days based on Numeric Pain Rating Scale
Numeric Pain Rating Scale. Minimum and maximum values are 0 and 10 points, respectively. Higher scores mean a worse outcome.
Baseline, 2nd week, 4th week, 6th week and 8th week
Cervical active range of motion
Dijital inclinometric measurements. Flexion, extension, right and left lateral flexions and right and left rotations.
From enrollment to the end of treatment at 8 weeks
Secondary Outcomes (2)
Hand grip strength
From enrollment to the end of treatment at 8 weeks
Cervical muscle performance
From enrollment to the end of treatment at 8 weeks
Study Arms (3)
Manual Therapy based Fascial Distortion Model
ACTIVE COMPARATORAll participants were given manual therapy based on the Fascial Distortion Model in addition to conventional therapy (Rocabado's 6x6 Exercises and Patient Education). Conventional therapy was implemented as a home program for 8 weeks, while Manual Therapy was conducted for forty-five minutes once a week in a clinical setting.
Core Stabilization Training
ACTIVE COMPARATORAll participants were given manual therapy based on the Core Stabilization Training in addition to conventional therapy (Rocabado's 6x6 Exercises and Patient Education). Conventional therapy was implemented as a home program for 8 weeks, while Core Stabilization Training was conducted for forty-five minutes once a week in a clinical setting.
Control
NO INTERVENTIONNo participant was given any therapy during the study.
Interventions
The following techniques were used on the cranial and cervical areas during therapy: Trigger band technique, herniated trigger point technique, continuum technique, folding technique, cylinder technique, and tectonic technique.
Resting position of the tongue, rotational control of temporomandibular joint, rhythmic stabilization, axial extension of the neck, shoulder posture, and stabilized head flexion
Participants are instructed to perform some behaviors while avoiding others based on the etiology of temporomandibular disorders.
Week 1st (1 x 10 reps): Supine deep cervical activation, supine deep lumbar activation, prone deep cervical activation, prone deep lumbar activation, supine combined deep cervical and lumbar activation, and prone combined deep cervical and lumbar activation; Week 2nd (1 x 10 reps): Arm openings, hundreds 1, one leg stretch 1, double leg stretch 1, shoulder bridge, breaststroke, leg pull prone prep 1; Week 3rd (1 x 10 reps): Arm openings, hundreds 2, one leg stretch 2, double leg stretch 2, shoulder bridge, breaststroke, leg pull prone prep 2; Week 4th (1 x 10 reps): Arm openings, hundreds 2, one leg stretch 2, double leg stretch 3, shoulder bridge, breaststroke, leg pull prone prep 2; Week 5th to 8th (with Resistance Band; 1 x 10 reps): Arm openings, shoulder bridge, swan dive, scapula isolations, plough, biceps curl, roll up, roll up with biceps, roll up with rowing, seated spine twist, swimming in kneeling, one leg kick in kneeling and diamond press in standing
Eligibility Criteria
You may qualify if:
- Having a temporomandibular joint complaint that has persisted for three months
- Being diagnosed with temporomandibular disorder according to the Diagnostic Criteria for Temporomandibular Disorders (DC/TMD) Axis I
- Comprehension and interest in responding to assessment questions
You may not qualify if:
- Having a systemic condition (neurological, rheumatological, oncological, etc.) that could affect the temporomandibular joint and/or interfere with the evaluation
- History of any trauma that may have affected cranial, cervical, or facial region
- Having undergone any surgical intervention in cranial, cervical, or facial regions in the previous six months
- Receiving any surgical treatment, medical treatment, or physiotherapy for temporomandibular disorder in the last month
- Having received radiotherapy in the cranial or cervical region
- Pregnancy or breastfeeding
- Exercise for head posture for the last month
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Hacettepe Universitylead
- Karabuk Universitycollaborator
Study Sites (2)
Hacettepe University
Ankara, 06100, Turkey (Türkiye)
Karabük University
Karabük, 78050, Turkey (Türkiye)
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Harun Gençosmanoğlu, PT, MSc
Karabük University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
December 17, 2023
First Posted
January 2, 2024
Study Start
December 17, 2023
Primary Completion
March 30, 2024
Study Completion
January 2, 2025
Last Updated
March 13, 2025
Record last verified: 2024-07
Data Sharing
- IPD Sharing
- Will not share