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Postural DisordersMYOPOST-FACENCT07610200

Effects of Myofascial Release Therapy on Body Posture and Facial Symmetry

A study testing Myofascial Release Therapy in people with Postural Disorders and Facial Asymmetry, run by Ece ACAR.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial 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. Read more about this study

Who is it for?
Ages 18 to 45 yearsHealthy volunteers can take part
What is being tested?
Myofascial Release Therapy
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
No sites listed yet
Study dates
15 Jun 2026to 1 Dec 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 45 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • 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

Who cannot join

  • 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

Trial locations and contacts

No sites are listed yet. Contact the study team or a site near you to ask about taking part.

Ece Acar, Assistant Professor, Physiothe contact

+905457925035

eceacar@karabuk.edu.tr

Eylül ESEN, MsC contact

+905385799415

eylulesennnn@gmail.com

About this study

Official title: Effects of Myofascial Release Therapy on Body Posture and Facial Symmetry in Healthy Individuals: A Randomized Controlled Trial

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.

Read more

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.

Read the detailed description

Body posture and fascial balance are closely associated with musculoskeletal health and biomechanical alignment. Impairments in postural alignment may contribute to abnormal loading patterns, muscular imbalance, fascial tension, and compensatory movement strategies throughout the body. Recent fascial theories suggest that fascial continuity may influence not only spinal and extremity alignment but also craniofacial structures and facial symmetry. Increased fascial tension, particularly in the cervical and thoracic regions, may alter soft tissue mechanics and contribute to asymmetrical facial appearance.

Myofascial release therapy is a manual therapy approach commonly used in physiotherapy to improve fascial mobility, decrease tissue restriction, reduce pain, and optimize postural alignment. Although previous studies have investigated the effects of myofascial interventions on musculoskeletal pain and posture, limited evidence exists regarding their influence on facial symmetry and facial anthropometric characteristics.

The present study is designed as a randomized controlled trial to evaluate the effects of myofascial release therapy on body posture and facial symmetry in healthy individuals. A total of 60 participants will be recruited and randomly allocated into intervention and control groups using a stratified randomization method based on dominant side characteristics. The intervention group will receive myofascial release therapy twice weekly for 6 weeks, whereas the control group will undergo only observation and assessment procedures during the same period.

The myofascial intervention protocol will include standardized manual therapy techniques targeting cervical, thoracic, shoulder, and fascial regions. The techniques will consist of single arm pull, lateral neck shoulder release, thoracic transverse plane technique, and anterior cervical fascial release applications performed by a trained physiotherapist.

Body posture assessment will be performed using the validated PostureScreen Mobile application. Standardized anterior, posterior, and lateral photographs will be analyzed to evaluate postural alignment parameters including forward head posture, shoulder asymmetry, spinal alignment, pelvic tilt, thoracic kyphosis, lumbar lordosis, and lower extremity alignment characteristics.

Facial symmetry assessment will be conducted using standardized digital facial photographs obtained under controlled environmental conditions. Anthropometric facial landmarks including exocanthion, endocanthion, alare, cheilion, zygion, and gonion points will be identified. Linear, proportional, and angular measurements will be calculated to determine facial asymmetry levels. Directional asymmetry scores will also be calculated to quantitatively evaluate right-left facial asymmetry.

Primary outcome measures will include changes in facial directional asymmetry scores and postural alignment parameters after the intervention period. Secondary analyses will investigate the relationship between postural characteristics, dominant side, physical activity habits, and facial symmetry variables.

The findings of this study may contribute to understanding the biomechanical relationship between fascial interventions, posture, and craniofacial symmetry. Additionally, the results may provide preliminary evidence for the use of fascial-based physiotherapy approaches in postural rehabilitation and facial asymmetry management.

Being tested
Myofascial Release Therapy
Keywords
Myofascial Release Therapy, Posture, Facial Symmetry, Fascial System, Manual Therapy, Postural Alignment, Physiotherapy, Facial Asymmetry, Myofascial Dysfunction, Randomized Controlled Trial
Medical subject headings
Facial Asymmetry

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Myofascial Release TherapyProcedure or surgery

    Also called Myofascial Therapy, Fascial Release Therapy, Manual Myofascial Release

    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.

Study groups in NCT07610200
Study groupRoleWhat they receive
Myofascial Release Therapy GroupExperimentalParticipants 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.
Receives: Procedure: Myofascial Release Therapy
Control GroupNo interventionParticipants in the control group will not receive any manual therapy or physical intervention during the study period and will only undergo assessment procedures.

What is being measured

The primary outcome is the main question the study is designed to answer.

  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.

    Measured: Baseline and after 6 weeks of intervention

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 May 2026
  2. Study start15 Jun 2026 (estimated)
  3. Primary completion1 Feb 2027 (estimated)
  4. Study completion1 Dec 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Participants will be randomly assigned to either the intervention group or the control group using a parallel-group design. The intervention group will receive myofascial release therapy twice weekly for 6 weeks, while the control group will undergo observation and assessment only. Outcome assessments will be performed at baseline and after completion of the intervention period.
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07610200
Sponsor's protocol ID
MYOPOSTFACE-RCT-2026
Acronym
MYOPOST-FACE
Status last verified
May 2026
First submitted
20 May 2026
Last updated
27 May 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided: Individual participant data sharing has not yet been determined. Data sharing decisions will be evaluated after study completion in accordance with institutional policies, ethical considerations, and publication requirements.

Publications

  • 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.

    PubMed 29410561
  • Wilke 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.

    PubMed 26281953
  • Schleip 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.

    PubMed 23036881

Questions about this trial

What is this clinical trial studying?

A study testing Myofascial Release Therapy in people with Postural Disorders and Facial Asymmetry, run by Ece ACAR.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 27 May 2026. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Ece Acar, Assistant Professor, Physiothe (+905457925035, eceacar@karabuk.edu.tr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in Facial Directional Asymmetry Score (time frame: Baseline and after 6 weeks of intervention). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07610200, which also lists 3 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 May 2026.

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