Effects of Myofascial Release Therapy on Body Posture and Facial Symmetry
MYOPOST-FACE
1 other identifier
interventional
60
0 countries
N/A
Brief Summary
This randomized controlled study aims to investigate the effects of myofascial release therapy on body posture and facial symmetry in healthy individuals. Postural disorders and fascial tension may lead to biomechanical alterations not only in the musculoskeletal system but also in facial soft tissues and symmetry. Myofascial release techniques are widely used in physiotherapy to improve fascial mobility, reduce tissue tension, and support postural alignment. However, the potential effects of these interventions on facial symmetry have not been sufficiently investigated. A total of 60 healthy participants will be included in the study and randomly assigned to either an intervention group or a control group. Participants in the intervention group will receive myofascial release therapy twice weekly for 6 weeks, while the control group will not receive any physical intervention during the same period. Body posture and facial symmetry assessments will be performed at baseline and after the intervention period. Postural assessment will be conducted using the PostureScreen Mobile application through standardized anterior, posterior, and lateral photographs. Facial symmetry will be evaluated using anthropometric facial landmarks identified on standardized facial photographs. Directional asymmetry scores, linear measurements, proportional analyses, and angular measurements will be calculated. The study is expected to provide evidence regarding the relationship between fascial interventions, postural alignment, and facial symmetry, and may contribute to the development of new physiotherapy approaches targeting fascial and postural dysfunctions.
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 Jun 2026
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
May 20, 2026
CompletedFirst Posted
Study publicly available on registry
May 27, 2026
CompletedStudy Start
First participant enrolled
June 15, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 1, 2027
May 27, 2026
May 1, 2026
8 months
May 20, 2026
May 20, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in Facial Directional Asymmetry Score
Facial symmetry will be evaluated using standardized digital facial photographs and anthropometric facial landmarks. Directional asymmetry scores will be calculated by comparing right and left facial measurements before and after the intervention period.
Baseline and after 6 weeks of intervention
Study Arms (2)
Myofascial Release Therapy Group
EXPERIMENTALParticipants in this group will receive myofascial release therapy twice weekly for 6 weeks. The intervention protocol will include cervical, thoracic, shoulder, and fascial manual therapy techniques performed by a trained physiotherapist.
Control Group
NO INTERVENTIONParticipants in the control group will not receive any manual therapy or physical intervention during the study period and will only undergo assessment procedures.
Interventions
Participants assigned to the intervention group will receive standardized myofascial release therapy performed by a trained physiotherapist twice weekly for 6 weeks. The intervention protocol will include single arm pull, lateral neck shoulder release, thoracic transverse plane technique, and anterior cervical fascial release techniques targeting cervical, thoracic, shoulder, and fascial regions. Each session will be conducted under standardized clinical conditions to improve fascial mobility, reduce tissue tension, and support postural alignment and facial symmetry.
Eligibility Criteria
You may qualify if:
- Healthy individuals aged between 18 and 45 years
- Ability to understand and follow study instructions
- Independent performance of daily living activities
- No regular physiotherapy or manual therapy treatment within the previous 3 months
- Willingness to participate voluntarily and sign the informed consent form
- Ability to attend assessment and intervention sessions regularly
You may not qualify if:
- History of neurological or orthopedic disorders affecting posture or facial symmetry
- Current musculoskeletal injury or ongoing rehabilitation treatment
- Previous facial, spinal, or major musculoskeletal surgery or trauma
- Pregnancy
- Use of medications affecting muscle tone or neuromuscular function
- Psychiatric or cognitive disorders limiting study participation
- Inability to comply with study procedures
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Ece ACARlead
Related Publications (3)
Szucs KA, Brown EVD. Rater reliability and construct validity of a mobile application for posture analysis. J Phys Ther Sci. 2018 Jan;30(1):31-36. doi: 10.1589/jpts.30.31. Epub 2018 Jan 27.
PMID: 29410561BACKGROUNDWilke J, Krause F, Vogt L, Banzer W. What Is Evidence-Based About Myofascial Chains: A Systematic Review. Arch Phys Med Rehabil. 2016 Mar;97(3):454-61. doi: 10.1016/j.apmr.2015.07.023. Epub 2015 Aug 14.
PMID: 26281953BACKGROUNDSchleip R, Jager H, Klingler W. What is 'fascia'? A review of different nomenclatures. J Bodyw Mov Ther. 2012 Oct;16(4):496-502. doi: 10.1016/j.jbmt.2012.08.001. Epub 2012 Aug 22.
PMID: 23036881BACKGROUND
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Ece Acar
Karabuk University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- Outcome assessors analyzing posture photographs and facial symmetry measurements will be blinded to group allocation. Participants and therapists providing the intervention will not be blinded due to the nature of the manual therapy application.
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Assistant Professor, Department of Physiotherapy and Rehabilitation
Study Record Dates
First Submitted
May 20, 2026
First Posted
May 27, 2026
Study Start
June 15, 2026
Primary Completion (Estimated)
February 1, 2027
Study Completion (Estimated)
December 1, 2027
Last Updated
May 27, 2026
Record last verified: 2026-05