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Phototherapy Applied in Association With Muscular Training

18 de octubre de 2016 actualizado por: Adriane Aver Vanin, University of Nove de Julho

Phototherapy Applied in Association With Muscular Training: Evaluation of Different Moments of Applications

The effects of phototherapy has been widely studied by some research groups. The investigators know that there are positive results with light application to improve muscle performance and delay fatigue. However, there are few studies showing its´ effects on muscular training. Therefore, the aim of this study was to assess the effects of phototherapy applied at different times during 12 weeks of strength training. For such, 48 volunteers, healthy male, from 18 to 35 years old were recruited to perform a strength training protocol for the anterior muscle of the thigh development. Volunteers performed the training protocol three times a week for 12 weeks. There were assessed isometric peak torque in isokinetic dynamometer, concentric peak torque, 1-repetition maximum test in the leg extension and leg press machines and bilateral thigh perimetry.

Descripción general del estudio

Estado

Terminado

Condiciones

Descripción detallada

This is a clinical, randomized, controlled placebo and double-blind study. Forty-eight participants performed muscular training protocol. Subjects practiced a protocol training with 60% of the load followed by 80% of the load, measured through 1-repetition maximum test, in all sessions of the training protocol. The training protocol consisted in performing 3 sets of 7 repetitions with 60% of 1-RM, and 4 set of 7 repetitions with 80% of 1-RM. This protocol was performed in every sessions, three times a week, employing leg press and leg extension machines.

Phototherapy, active or placebo, were applied in 6 different points of anterior muscle of the thigh before and after each training session. Only one investigator, that did not participate in any phase of the assessments and trainings sessions, knew about what program is active or placebo in phototherapy device. Randomisation carried out by a simple drawing of lots (A, B, C, or D) in the first visit. The phototherapy unit emitted the same sound regardless of the program used, active or placebo. Either strength training lasted 12 weeks and assessments were performed at baseline, 4, 8 and 12 weeks. There were evaluated maximal voluntary contraction (MVC), concentric torque, bilateral thigh perimetry and 1-repetition maximum test (1-RM).

Tipo de estudio

Intervencionista

Inscripción (Actual)

48

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.

Ubicaciones de estudio

    • SP
      • São Paulo, SP, Brasil, 01504-001
        • Universidade Nove de Julho

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

18 años a 35 años (Adulto)

Acepta Voluntarios Saludables

Géneros elegibles para el estudio

Masculino

Descripción

Inclusion Criteria:

  • healthy individuals,
  • active, that performed less than two exercise sessions per week
  • when they presented musculoskeletal injury to the hips or knees in the previous 2 months,
  • used pharmacological agents or nutritional supplements regularly, and
  • Subjects that did not attend a minimum rate of 80% of all strength training sessions
  • Suffered musculoskeletal injury during the ongoing of the study were also excluded.

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: Cuidados de apoyo
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Cuadruplicar

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Group A - Active or Placebo Phototherapy

Participants enrolled in this group performed a training protocol for 12 weeks with light application before and after the exercise protocol. The phototherapy device was divided in program 1 and program 2. One of these programs consisted in active phototherapy and the other placebo.

The subjects allocated in group A, received program 1 before strength training, and the same program 1 after training.

Otros nombres:
  • Dispositivo MR4: dispositivo que combina láseres súper pulsados ​​y LED rojos e infrarrojos (Multi Radiance Medical, Solon, OH, EE. UU.)
Experimental: Group B - Active or Placebo Phototherapy

Participants enrolled in this group performed a training protocol for 12 weeks with light application before and after the exercise protocol. The phototherapy device was divided in program 1 and program 2. One of these programs consisted in active phototherapy and the other placebo.

The subjects allocated in group B, received program 1 before strength training, and program 2 after training.

Otros nombres:
  • Dispositivo MR4: dispositivo que combina láseres súper pulsados ​​y LED rojos e infrarrojos (Multi Radiance Medical, Solon, OH, EE. UU.)
Experimental: Group C - Active or Placebo Phototherapy

Participants enrolled in this group performed a training protocol for 12 weeks with light application before and after the exercise protocol. The phototherapy device was divided in program 1 and program 2. One of these programs consisted in active phototherapy and the other placebo.

The subjects allocated in group C, received program 2 before strength training, and program 1 after training.

Otros nombres:
  • Dispositivo MR4: dispositivo que combina láseres súper pulsados ​​y LED rojos e infrarrojos (Multi Radiance Medical, Solon, OH, EE. UU.)
Experimental: Group D - Active or Placebo Phototherapy

Participants enrolled in this group performed a training protocol for 12 weeks with light application before and after the exercise protocol. The phototherapy device was divided in program 1 and program 2. One of these programs consisted in active phototherapy and the other placebo.

The subjects allocated in group D, received program 2 before strength training, and program 2 after training.

Otros nombres:
  • Dispositivo MR4: dispositivo que combina láseres súper pulsados ​​y LED rojos e infrarrojos (Multi Radiance Medical, Solon, OH, EE. UU.)

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change from baseline Maximum voluntary contraction in the isokinetic dynamometer (MVC) at 12 weeks
Periodo de tiempo: 12 weeks
Functional performance measure - performed in baseline, 4 weeks, 8 weeks and 12 weeks after the beginning of the muscular training
12 weeks
Change from baseline Concentric Torque at 12 weeks
Periodo de tiempo: 12 weeks
Functional performance measure - performed in baseline, 4 weeks, 8 weeks and 12 weeks after the beginning of the muscular training
12 weeks

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
1-RM test
Periodo de tiempo: 12 weeks
Functional performance measure - performed in baseline, 4 weeks, 8 weeks and 12 weeks after the beginning of the muscular training. This test estimated the load of the exercises.
12 weeks

Otras medidas de resultado

Medida de resultado
Medida Descripción
Periodo de tiempo
Thigh perimetry
Periodo de tiempo: 12 weeks
Muscle mass measure - performed in baseline, 4 weeks, 8 weeks and 12 weeks after the beginning of the muscular training.
12 weeks

Colaboradores e Investigadores

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

Investigadores

  • Director de estudio: Ernesto Leal-Junior, PhD, University of Nove de Julho

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

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

1 de marzo de 2016

Finalización primaria (Actual)

1 de agosto de 2016

Finalización del estudio (Actual)

1 de octubre de 2016

Fechas de registro del estudio

Enviado por primera vez

11 de marzo de 2016

Primero enviado que cumplió con los criterios de control de calidad

16 de marzo de 2016

Publicado por primera vez (Estimar)

22 de marzo de 2016

Actualizaciones de registros de estudio

Última actualización publicada (Estimar)

20 de octubre de 2016

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

18 de octubre de 2016

Última verificación

1 de octubre de 2016

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • PhD437.894

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. .

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