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

31 août 2026 mis à jour par: 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.

Aperçu de l'étude

Statut

Recrutement

Les conditions

Description détaillée

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.

Type d'étude

Observationnel

Inscription (Estimé)

60

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Sauvegarde des contacts de l'étude

Lieux d'étude

    • Beitun
      • Taichung, Beitun, Taïwan, 406040
        • Recrutement
        • Department of Physical Therapy, China Medical University
        • Contact:
        • Contact:
        • Chercheur principal:
          • Yueh-Ling Hsieh, PhD

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte

Accepte les volontaires sains

Oui

Méthode d'échantillonnage

Échantillon non probabiliste

Population étudiée

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.

La description

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

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

Cohortes et interventions

Groupe / Cohorte
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.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Hexagon Agility Test Completion Time
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

1 avril 2026

Achèvement primaire (Estimé)

31 janvier 2027

Achèvement de l'étude (Estimé)

28 février 2027

Dates d'inscription aux études

Première soumission

26 août 2026

Première soumission répondant aux critères de contrôle qualité

31 août 2026

Première publication (Réel)

1 septembre 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

1 septembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

31 août 2026

Dernière vérification

1 août 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • CMUH115-REC3-011
  • NSTC115-2813-C-039-101-B (Autre subvention/numéro de financement: National Science and Technology Council)

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Description du régime 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.

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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