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Effects of Myofascial Release Therapy on Body Posture and Facial Symmetry (MYOPOST-FACE)

20 de maio de 2026 atualizado por: Ece ACAR

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.

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.

Visão geral do estudo

Status

Ainda não está recrutando

Descrição detalhada

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.

Tipo de estudo

Intervencional

Inscrição (Estimado)

60

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

  • Nome: Ece Acar, Assistant Professor, Physiothe
  • Número de telefone: +905457925035
  • E-mail: eceacar@karabuk.edu.tr

Estude backup de contato

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto

Aceita Voluntários Saudáveis

Sim

Descrição

Inclusion Criteria:

  • 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

Exclusion Criteria:

  • 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

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Solteiro

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Myofascial Release Therapy Group
Participants 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.
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.
Outros nomes:
  • Lançamento miofascial manual
  • Myofascial Therapy
  • Fascial Release Therapy
Sem intervenção: Control Group
Participants in the control group will not receive any manual therapy or physical intervention during the study period and will only undergo assessment procedures.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Change in Facial Directional Asymmetry Score
Prazo: Baseline and after 6 weeks of intervention
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

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Patrocinador

Investigadores

  • Investigador principal: Ece Acar, Karabuk University

Publicações e links úteis

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Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

15 de junho de 2026

Conclusão Primária (Estimado)

1 de fevereiro de 2027

Conclusão do estudo (Estimado)

1 de dezembro de 2027

Datas de inscrição no estudo

Enviado pela primeira vez

20 de maio de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

20 de maio de 2026

Primeira postagem (Real)

27 de maio de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

27 de maio de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

20 de maio de 2026

Última verificação

1 de maio de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

INDECISO

Descrição do plano IPD

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.

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

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