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Full-Body and Lower-Limb Stretching on Explosive Power and Agility (static stretch)

31 de agosto de 2026 atualizado por: Yueh-Ling Hsieh, China Medical University Hospital

Do Stretching Variations Affect Performance? A Comparison of Full-Body and Lower-Limb Stretching on Explosive Power and Agility Reaction Time

Stretching is commonly used during warm-up and recovery and can influence flexibility, neuromuscular control, and joint range of motion. However, the acute effects of different stretching scopes on jump and agility performance remain unclear. This study will compare whole-body and lower-limb static stretching in 60 healthy university students randomly assigned to whole-body stretching, lower-limb stretching, or control groups. Each intervention will last 14 minutes. Jump performance will be assessed using the standing long jump, squat jump, countermovement jump, and drop jump with a Vmaxpro sensor, while agility will be evaluated using the T-Test and Hexagon Agility Test. The findings are expected to clarify how stretching scope influences acute physical performance and may inform warm-up and physical therapy strategies.

Visão geral do estudo

Status

Recrutamento

Condições

Descrição detalhada

Stretching exercise is one of the most commonly used strategies for pre-exercise warm-up and post-exercise recovery, and its physiological effects involve muscle flexibility, neuromuscular control, and joint range of motion. However, empirical evidence regarding the acute effects of different stretching scopes on jumping ability and agility remains relatively limited, as most previous studies have focused on individual muscles or localized muscle groups. Therefore, the present study aims to investigate the effects of static stretching involving different body regions, specifically whole-body and lower-limb stretching, on explosive performance and agility.

A pretest-intervention-posttest design will be adopted. A total of 60 healthy university students (30 males and 30 females) are expected to be recruited and randomly assigned to a whole-body stretching group (10 males and 10 females), a lower-limb stretching group (10 males and 10 females), or a control group (10 males and 10 females). The duration of the static stretching intervention will be standardized to 14 minutes. The whole-body stretching group will perform stretching exercises targeting the major muscle groups of the upper limbs, trunk, and lower limbs, whereas the lower-limb stretching group will focus on key lower-limb muscle groups, including the quadriceps, hamstrings, and gastrocnemius. The control group will remain seated quietly for 14 minutes without performing any stretching exercise.

Participants will undergo a series of physical performance assessments before and after the intervention. Jump performance will be evaluated using the standing long jump, squat jump, countermovement jump, and drop jump. All jump-related data will be recorded using a Vmaxpro wireless inertial measurement sensor (BM Sports Technology GmbH, Germany), providing key parameters such as jump height, peak velocity, and peak power. Agility will be assessed using the T-Test and Hexagon Agility Test.

It is hypothesized that excessive static stretching may cause an acute reduction in muscular strength and explosive performance. The whole-body stretching group may demonstrate only a slight decrease in jump performance while maintaining relatively stable agility performance, whereas the lower-limb stretching group may exhibit changes in both jump and agility performance. The findings of this study are expected to clarify the relationship between the scope of static stretching and subsequent physical performance and may provide evidence to support the design of pre-exercise warm-up strategies and physical therapy interventions.

Tipo de estudo

Observacional

Inscrição (Estimado)

60

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

Estude backup de contato

Locais de estudo

    • Beitun
      • Taichung, Beitun, Taiwan, 406040
        • Recrutamento
        • Department of Physical Therapy, China Medical University
        • Contato:
        • Contato:
        • Investigador principal:
          • Yueh-Ling Hsieh, PhD

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

Método de amostragem

Amostra Não Probabilística

População do estudo

Healthy university students aged 18-30 years who are able to safely perform jumping and agility tasks will be recruited from the university community. Participants with recent musculoskeletal injuries, relevant surgery, cardiovascular disease, exercise contraindications, or conditions affecting test performance will be excluded.

Descrição

Healthy university students aged 20-30 years Regularly engaged in physical activity Not specialized in weightlifting or jumping disciplines Able to understand the study procedures and provide written informed consent

Exclusion Criteria:

Acute lower-limb or low-back injury within the previous three months Fracture, sprain, or muscle strain within the previous three months Related surgery or medical treatment within the previous three months Pain, swelling, inflammation, or restricted movement on the day of testing Any condition that may compromise exercise safety Physician-advised restriction from moderate- to high-intensity exercise Cardiovascular disease or other exercise contraindications Neurological, musculoskeletal, or balance impairments that may affect test performance

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

Coortes e Intervenções

Grupo / Coorte
Whole-Body Stretching
Healthy university students who performed the whole-body static stretching protocol.
Lower-Limb Stretching Group
Healthy university students who performed the lower-limb static stretching protocol.
Non-Stretching Control Group
Healthy university students who remained seated quietly without performing stretching exercises.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Hexagon Agility Test Completion Time
Prazo: From baseline to immediately after the 15-min intervention
Agility performance will be assessed using the Hexagon Agility Test. Participants will complete two valid trials, and the mean completion time will be used for analysis. Completion time will be recorded in seconds, with a shorter time indicating better agility performance.
From baseline to immediately after the 15-min intervention
T-Test Agility Test Completion Time
Prazo: From baseline to immediately after the 15-min intervention
Agility performance will be assessed using the T-Test Agility Test. Participants will complete two trials, and completion time will be recorded in seconds using a photocell timing gate system. The mean completion time of the two trials will be used for analysis, with lower values indicating better agility performance.
From baseline to immediately after the 15-min intervention
Squat jump height
Prazo: From baseline to immediately after the 15-min intervention
Squat jump performance will be assessed using a wireless inertial measurement sensor. Participants will perform two valid squat jump trials, and the mean jump height will be used for analysis. Jump height will be recorded in centimeters, with higher values indicating better jump performance.
From baseline to immediately after the 15-min intervention
Countermovement Jump Height
Prazo: From baseline to immediately after the 15-min intervention
Countermovement jump performance will be assessed using a wireless inertial measurement sensor. Participants will perform two valid countermovement jump trials, and the mean jump height will be used for analysis. Jump height will be recorded in centimeters, with higher values indicating better jump performance.
From baseline to immediately after the 15-min intervention
Drop Jump Reactive Strength Index
Prazo: From baseline to immediately after the 15-min intervention
Reactive strength during the drop jump will be assessed using a wireless inertial measurement sensor. The reactive strength index will be calculated as jump height divided by ground contact time. Participants will perform two valid trials, and the mean reactive strength index will be used for analysis. Values will be expressed in meters per second, with higher values indicating better reactive strength performance.
From baseline to immediately after the 15-min intervention
Standing Long Jump Distance
Prazo: From baseline to immediately after the 15-min intervention
Horizontal lower-limb explosive performance will be assessed using the standing long jump. Participants will perform two valid trials, and the mean jump distance will be used for analysis. Jump distance will be recorded in centimeters, with higher values indicating better performance.
From baseline to immediately after the 15-min intervention

Colaboradores e Investigadores

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Patrocinador

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 (Real)

1 de abril de 2026

Conclusão Primária (Estimado)

31 de janeiro de 2027

Conclusão do estudo (Estimado)

28 de fevereiro de 2027

Datas de inscrição no estudo

Enviado pela primeira vez

26 de agosto de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

31 de agosto de 2026

Primeira postagem (Real)

1 de setembro de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

1 de setembro de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

31 de agosto de 2026

Última verificação

1 de agosto de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • CMUH115-REC3-011
  • NSTC115-2813-C-039-101-B (Número de outro subsídio/financiamento: National Science and Technology Council)

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Descrição do plano IPD

Individual participant data are not planned for public sharing. De-identified data may be made available from the corresponding author upon reasonable request, subject to applicable ethical and institutional 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

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .