Esta página se tradujo automáticamente y no se garantiza la precisión de la traducción. por favor refiérase a versión inglesa para un texto fuente.

Effect of Adding Thoracolumbar Fascia Release by IASTM to Conventional Treatment on Craniovertebral Angle in Forward Head Subjects (IASTM)

18 de mayo de 2026 actualizado por: Mariam Mohamed, Cairo University

Influence of Thoracolumbar Fascial Release by Instrument Assisted Soft Tissue Moblization on Craniovertebral Angle in Forward Head Posture

The Posture Committee of the American Academy of Orthopedic Surgery defines good posture as "that state of muscular and skeletal balance that protects the supporting structures of the body against injury or progressive deformity irrespective of the attitude (erect, lying, squatting, and stooping) in which these structures are working or resting." Under those conditions, the muscles will function most efficiently, and the Thoracic and abdominal organs will be in their optimal places.

Descripción general del estudio

Estado

Reclutamiento

Descripción detallada

The FHP is expected to have a major impact on respiratory function by weakening the accessory respiratory muscles. Persistent FHP weakens the muscles involved in breathing, leading to a decline in respiratory function. Also, it was suggested that FHP is quite common in undergraduate students and has significant effect on level of stress.

A vital component of the myofascial girdle envelops the lower torso, thoracolumbar fascia, participates in posture, load transfer, and breathing. The deep muscles at the back of the spine and the muscles in the abdomen are covered by the TLF. The latissimus dorsi, gluteus maximus, and other muscles in the area are related to a few muscles that engage in the movement of the proximal limbs, and the TLF functions as a force-transmitting structure.

When the upper extremities are impacted, the thoracolumbar fascia release (TLFR) technique should be considered, however, there has not been much research that uses TLFR for the upper extremities. The TLF works together by connecting with the deep core muscles. The medium and posterior parts of the TLF form the transversus abdominis, and the deep lamina is associated with the lumbar spinous processes .

The deep posterior layer continues cranially by merging with the splenius cervicis fascia. Therefore, TLF plays a role in Cervical region mobility. The TLFR increased bilateral sternocleidomastoid muscle resistance and decreased head-forward posture angle in the short term in young women with head-forward posture .

Another novel technique that is quickly gaining traction is IASTM, which allows physicians to treat patients with soft tissue dysfunction in a non-invasive manner. By remodeling connective tissue, resorbing excess fibrosis, recruiting fibroblasts, and inducing collagen repair and regeneration, IASTM mobilizes connective tissue and myofascial adhesions using specially designed instruments. The use of IASTM is recommended to improve the range of motions in healthy individuals, reduce pain in patients with musculoskeletal injuries.

However, there is a gap of empirical data establishing the effect of adding TLF release by IASTM to conventional treatment protocol of FHP on CVA, Cervical ROM, Cervical proprioception and stress level.

Therefore, this study sought to determine the effect of adding TLFR to conventional treatment protocol of FHP to improve CVA, Cervical ROM, Cervical proprioception and stress level.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

30

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

  • Nombre: Mariam M Abdallah, Assistant lecturer
  • Número de teléfono: +201221337723
  • Correo electrónico: mariam.youssef@cu.edu.eg

Copia de seguridad de contactos de estudio

Ubicaciones de estudio

    • Giza Governorate
      • Giza, Giza Governorate, Egipto, 12611
        • Reclutamiento
        • Faculty of Physical Therapy
        • Investigador principal:
          • Ragia M kamel, professor
        • Sub-Investigador:
          • Mary K Nassif, Assistant professor
        • Sub-Investigador:
          • Aya M Mohamed, lecturer

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto

Acepta Voluntarios Saludables

No

Descripción

Inclusion Criteria:

  • Forward head posture subjects with CVA of < 52
  • Subject's age ranged from 18-30 years old, with Body Mass Index (BMI) less than 30Kg/m2.
  • Pain-free subjects for over 3 months, No PT intervention. Exclusion Criteria;

    1. Osteoporotic disorder.
    2. Any history of congenital deformities of the Cervical and Thoracic region.
    3. Recent injuries or fractures.
    4. Any inflammatory joint disorder.
    5. Malignancy.
    6. Vascular disorders.
    7. Neurological or psychiatric disorders.
    8. Any respiratory disease, presence of open wound/s, or history of surgery in the past 6 months.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Único

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Otro: control group

Control group (conventional treatment protocol):

The control group will receive firstly, Kendall exercises; every strengthening exercise will be repeated for 12 repetitions and done for 3 sets and each stretching exercise will be held for 30 seconds and repeated 3 times.

Then, participants will receive IASTM application on cervical muscles as follows: IASTM for upper fibers of trapezius, levator scapulae muscles and scalnae.

Instrument-assisted soft tissue mobilization (IASTM) is a special instrument with beveled edges to assist the clinician in the evaluation and mobilization of soft tissue. Instruments are used in a multi directional stroking fashion applied to the skin at 30°-60° angles to detect soft tissue irregularities via the undulation of the tools. It has been purported to enhance proliferation of extracellular matrix fibro blasts, improve ion transport, and decrease cell matrix adhesions
Otros nombres:
  • IASTM
Experimental: experimental group
participants will receive same protocol as control group (IASTM on cervical muscles and Kendel exercises) in addition to Thoraco lumber fascia release using IASTM tool
Instrument-assisted soft tissue mobilization (IASTM) is a special instrument with beveled edges to assist the clinician in the evaluation and mobilization of soft tissue. Instruments are used in a multi directional stroking fashion applied to the skin at 30°-60° angles to detect soft tissue irregularities via the undulation of the tools. It has been purported to enhance proliferation of extracellular matrix fibro blasts, improve ion transport, and decrease cell matrix adhesions
Otros nombres:
  • IASTM

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Craniovertebral angle(CVA)
Periodo de tiempo: measurement at Day 1 then after 1 month
Craniovertebral angle (CVA) is a line drawn from the tragus of the ear to the C7 vertebra intersects a horizontal line. It is used to measure the value of FHP, and the greater the value of this angle, the more forward the head is positioned on the neck. A vast variety of names exist for this angle, such as sagittal C7-tragus angle, sagittal plane head alignment, neck inclination angle, Cervical angle, head protrusion angle, head position, FHP, forward head position, and head anteriorization in relation to Cervical vertebra
measurement at Day 1 then after 1 month

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
cervical range of motion
Periodo de tiempo: measurement at Day 1 then after 1 month
flexion ,extension,sidebending ,rotation
measurement at Day 1 then after 1 month
cervical proprioception
Periodo de tiempo: measurement at Day 1 then after 1 month
flexion, extension,sidebending,rotation
measurement at Day 1 then after 1 month
Cohen perceived stress scale
Periodo de tiempo: measurement at Day 1 then after 1 month
Arabic version for stress scale
measurement at Day 1 then after 1 month

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

4 de marzo de 2026

Finalización primaria (Estimado)

18 de diciembre de 2026

Finalización del estudio (Estimado)

18 de enero de 2027

Fechas de registro del estudio

Enviado por primera vez

1 de mayo de 2026

Primero enviado que cumplió con los criterios de control de calidad

18 de mayo de 2026

Publicado por primera vez (Actual)

26 de mayo de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

26 de mayo de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

18 de mayo de 2026

Última verificación

1 de febrero de 2026

Más información

Términos relacionados con este estudio

Palabras clave

Otros números de identificación del estudio

  • Faculty of Physical Therapy CU

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

INDECISO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

producto fabricado y exportado desde los EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

Suscribir