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Foam Roller Compared to Massage on Reducing Calf Muscle Tone in Healthy Subjects (FRTONE)

26 de abril de 2026 actualizado por: Carlos Romero Morales, Universidad Europea de Madrid

Effect of Foam Roller Compared to Massage on Reducing Calf Muscle Tone in Healthy Subject

Objective: This study aims to compare the effects of two techniques-foam rolling (FR) and therapeutic massage-on reducing the muscle tone in the calf muscles (gastrocnemius and soleus) of healthy individuals.

Methods: A randomized, controlled crossover design was used with 40 healthy participants (aged 18-45). Participants were randomly assigned to either a foam roller or a therapeutic massage group. The interventions were applied to the dominant leg, and muscle tone was measured pre- and post-intervention using a MyotonPro device. The primary outcome was muscle tone (Hz), and secondary outcomes included muscle stiffness (N/m) and elasticity (D [log]).

Results: The study will assess the effectiveness of each intervention on muscle tone, stiffness, and elasticity. It aims to determine whether foam rolling is as effective or superior to traditional massage in reducing calf muscle tone.

Conclusion: This research will contribute to understanding the efficacy of foam rolling as a self-administered technique for muscle tone reduction and its potential application in clinical and athletic settings

Descripción general del estudio

Estado

Aún no reclutando

Intervención / Tratamiento

Tipo de estudio

Intervencionista

Inscripción (Estimado)

20

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

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
  • Adulto Mayor

Acepta Voluntarios Saludables

Sí

Descripción

Inclusion Criteria:

  1. Age: Participants aged between 18 and 45 years.
  2. Health Status: Healthy individuals with no prior musculoskeletal conditions in the lower limbs.
  3. Pain-Free: Participants should not have had pain in the gastrocnemius or Achilles tendon in the last 3 months.
  4. Willingness: Participants must provide informed consent and be available for the intervention and necessary evaluations.

Exclusion Criteria:

  1. Musculoskeletal Conditions: Individuals with any pathologies in the calf muscles (gastrocnemius, soleus) or Achilles tendon.
  2. Vascular or Neurological Issues: Participants with vascular diseases or neurological disorders that may interfere with the interventions or muscle response.
  3. Skin Conditions: Exclusion of participants with skin alterations, infections, or open wounds in the area of intervention.
  4. Pregnancy: Women who are pregnant.
  5. Sensitivity Issues: Participants with altered sensitivity in the lower limbs or any condition that may affect the response to the techniques.
  6. Non-Compliance: Individuals who do not provide informed consent or are not available for the required evaluations.

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: Prevención
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Foam roller

A foam roller is a cylindrical tool used for self-myofascial release (SMR), a technique that involves applying pressure to muscle groups to alleviate muscle tightness, improve flexibility, and reduce soreness. It is widely used in physical therapy, sports rehabilitation, and fitness routines. The foam roller is typically made from a dense foam material that allows for controlled compression of the muscles and fascia during rolling movements.

In the study, participants will use a foam roller to target the calf muscles (gastrocnemius and soleus) on their dominant leg. The foam roller technique consists of rolling the device along the targeted muscle areas in both directions-cranial to caudal (from the top to the bottom) and vice versa-at a slow, controlled pace (30 rolls per minute).

The foam roller is used for self-myofascial release (SMR) to reduce muscle tightness and improve flexibility. In this study, participants will use the foam roller on their dominant calf muscles, rolling it up and down at a controlled pace (30 rolls per minute). The pressure applied should be moderate, staying within a pain tolerance of 6/10 on the Visual Analogue Scale (VAS).

The technique is repeated three times, with a one-minute rest between sets. The goal is to enhance muscle relaxation and reduce muscle tone

Comparador activo: Massage

The therapeutic massage used in this study involves manual techniques to reduce muscle tone and improve flexibility in the calf muscles. It includes:

  1. Deep Gliding Stroke: Sliding from the upper to the lower part of the calf to relax the muscles.
  2. Soleus Compression: Applying pressure to the soleus muscle with the hands to release tension.
  3. Calf Compression: Applying pressure to specific points on the calf to alleviate stiffness.

Each technique lasts for 2 minutes, with a total intervention time of 8 minutes per participant. The goal is to reduce muscle tone and enhance relaxation

The therapeutic massage used in this study involves manual techniques to reduce muscle tone and improve flexibility in the calf muscles. It includes:

  1. Deep Gliding Stroke: Sliding from the upper to the lower part of the calf to relax the muscles.
  2. Soleus Compression: Applying pressure to the soleus muscle with the hands to release tension.
  3. Calf Compression: Applying pressure to specific points on the calf to alleviate stiffness.

Each technique lasts for 2 minutes, with a total intervention time of 8 minutes per participant. The goal is to reduce muscle tone and enhance relaxation

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Muscle tone
Periodo de tiempo: Pre and post intervention (immediately post foam roller procedure)
Description: Muscle tone refers to the continuous and passive tension in a muscle at rest, measured by its resistance to passive stretching. It is quantified in Hertz (Hz), indicating the frequency of oscillation when the muscle is in a relaxed state.
Pre and post intervention (immediately post foam roller procedure)

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Muscle stiffness
Periodo de tiempo: Pre intervention and post intervention (immediately after the foam roller procedure)
Description: Muscle stiffness is the resistance a muscle provides when stretched. It is measured in Newtons per meter (N/m) and reflects how much force is needed to deform the muscle. Higher stiffness indicates less flexibility.
Pre intervention and post intervention (immediately after the foam roller procedure)
Muscle elasticity
Periodo de tiempo: pre and post intervention (immediately after the interventions)
Description: Elasticity refers to a muscle's ability to return to its original shape after being stretched. It is measured using a logarithmic scale (D [log]), representing the rate of decrease in oscillation amplitude after a mechanical disturbance.
pre and post intervention (immediately after the interventions)

Colaboradores e Investigadores

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Publicaciones y enlaces útiles

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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 (Estimado)

15 de mayo de 2026

Finalización primaria (Estimado)

15 de junio de 2026

Finalización del estudio (Estimado)

15 de julio de 2026

Fechas de registro del estudio

Enviado por primera vez

26 de abril de 2026

Primero enviado que cumplió con los criterios de control de calidad

26 de abril de 2026

Publicado por primera vez (Actual)

4 de mayo de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

4 de mayo de 2026

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

26 de abril de 2026

Última verificación

1 de abril de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • CI-2026-338

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

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