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- Ensayo clínico NCT03698578
Creatine Kinase Levels and Clinical and Functional Parameters in Parajiu-jitsu Athletes
5 de octubre de 2018 actualizado por: Jaqueline Santos Silva, São Paulo State University
Correlation Between Creatine Kinase Levels and Clinical and Functional Parameters in the Moments Following the Fight in Parajiu-jitsu Athletes: A Controlled Clinical Trial
Introduction: Evidence indicates that muscle damage caused by exercise can lead to functional, biochemical and clinical damage.
Therefore, it is pertinent to perform investigations related to the muscle damage marker, creatine kinase with clinical and functional responses.
These outcomes encompass an intrinsic potential for understanding the real magnitude of interpretation of classic signals in athletic environments and monitoring of athletes, contributing to specific actions.
Objective: To verify the correlation between clinical signs (pain and perception of recovery), functional (muscular strength) and the behavior of CK levels, in the moments following a simulated fight.
METHODS: Six male parajiu-jitsu practitioners (34-44 years) were included in the study.
The participants attended the collection site 4 times, with a 24-hour interval between sessions, characterizing the following collection moments: baseline, post-exertion, 24, 48 and 72 hours after the simulated fight.
Data on pain (visual analogue scale - EVA), perception of recovery (Likert Scale), muscle strength (Dynamometry) and blood samples for CK analysis were collected.
All parameters described were measured at all times of collection.
For the analysis of the association between behavior of CK levels, clinical and functional variables, the Odds Ratio test and 95% confidence interval were used.
For the gross values, the Pearson test was used according to the normality of the data.
Descripción general del estudio
Estado
Desconocido
Condiciones
Intervención / Tratamiento
Descripción detallada
Participants will be intentionally allocated into two groups, G1 consisting of professional athletes and G2 consisting of amateur athletes.
This division was carried out to guarantee homogeneous stratification between participants with level of conditioning and similar training.
The anonymity of the participants will be guaranteed.
There will be masking of the participants, investigator and evaluator of the results that were blind to the hypotheses and allocation in groups, adopted in the study.
All participants regularly attended the same training center and no sports injuries that might compromise athletic performance will be reported during the survey.
Tipo de estudio
Intervencionista
Inscripción (Anticipado)
12
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: Jaqueline Lopes, master
- Número de teléfono: 66999202206
- Correo electrónico: jaqueee-santosss@hotmail.com
Copia de seguridad de contactos de estudio
- Nombre: Aryane Machado, master
- Número de teléfono: + 55 18 981156556
- Correo electrónico: ary_machado@hotmail.com
Ubicaciones de estudio
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Mount
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Barra do Garças, Mount, Brasil, 78600-000
- Reclutamiento
- Rayana Loch Gomes
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Contacto:
- Jaqueline Lopes
- Número de teléfono: 66999202206
- Correo electrónico: jaqueee-santosss@hotmail.com
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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 50 años (Adulto)
Acepta Voluntarios Saludables
Sí
Géneros elegibles para el estudio
Masculino
Descripción
Inclusion Criteria:
- Jiu-Jitsu paratroopers were included. To be included in the study participants should report absence of anemia, inflammation, diabetes, cardiovascular disease, and musculoskeletal injuries in the six months prior to data collection. In addition, participants were instructed to refrain from anti-inflammatory drugs, analgesics, alcoholic beverages, and tobacco and did not perform any extra exercise during the study.
Exclusion Criteria:
- withdrawal of participants for personal reasons
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: Poner en pantalla
- Asignación: No aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Triple
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
---|---|
Experimental: group 1 combat fight
Consisting of professional, high-performance paratletas.
Intervention: Jiu-jitsu heating with light intensity was used for 5 minutes.
The simulated fight protocol occurred in accordance with the rules of the Brazilian Confederation of Sports Jiu-Jitsu, excluding any types of finalization.
In these cases, the athletes were separated and oriented to return immediately.
Thus, maximum effort was advocated as well as, similar time of activity for all
|
Jiu-jitsu heating with light intensity was used for 5 minutes.
The simulated fight protocol occurred in accordance with the rules of the Brazilian Confederation of Sports Jiu-Jitsu, excluding any types of finalization.
In these cases, the athletes were separated and oriented to return immediately.
Thus, maximum effort was advocated as well as, similar time of activity for all
|
Experimental: group 2 combat fight
Constituted by amateur paratroopers.
Intervention: Jiu-jitsu heating with light intensity was used for 5 minutes.
The simulated fight protocol occurred in accordance with the rules of the Brazilian Confederation of Sports Jiu-Jitsu, excluding any types of finalization.
In these cases, the athletes were separated and oriented to return immediately.
Thus, maximum effort was advocated as well as, similar time of activity for all
|
Jiu-jitsu heating with light intensity was used for 5 minutes.
The simulated fight protocol occurred in accordance with the rules of the Brazilian Confederation of Sports Jiu-Jitsu, excluding any types of finalization.
In these cases, the athletes were separated and oriented to return immediately.
Thus, maximum effort was advocated as well as, similar time of activity for all
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
---|---|---|
creatine kinase
Periodo de tiempo: post fight - 72 hours
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blood collection
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post fight - 72 hours
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
---|---|---|
perception of recovery
Periodo de tiempo: post fight - 72 hours
|
scale
|
post fight - 72 hours
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muscle pain
Periodo de tiempo: post fight - 72 hours
|
scale
|
post fight - 72 hours
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Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Investigadores
- Silla de estudio: Jessica Michelletti, master, Paulista State University
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)
20 de septiembre de 2018
Finalización primaria (Anticipado)
20 de febrero de 2019
Finalización del estudio (Anticipado)
20 de marzo de 2019
Fechas de registro del estudio
Enviado por primera vez
4 de octubre de 2018
Primero enviado que cumplió con los criterios de control de calidad
5 de octubre de 2018
Publicado por primera vez (Actual)
9 de octubre de 2018
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
9 de octubre de 2018
Última actualización enviada que cumplió con los criterios de control de calidad
5 de octubre de 2018
Última verificación
1 de octubre de 2018
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- SaoPSU_UFMT1
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
NO
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
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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