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

31 agosto 2026 aggiornato da: 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.

Panoramica dello studio

Stato

Reclutamento

Condizioni

Descrizione dettagliata

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 di studio

Osservativo

Iscrizione (Stimato)

60

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

Luoghi di studio

    • Beitun
      • Taichung, Beitun, Taiwan, 406040
        • Reclutamento
        • Department of Physical Therapy, China Medical University
        • Contatto:
        • Contatto:
        • Investigatore principale:
          • Yueh-Ling Hsieh, PhD

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto

Accetta volontari sani

Sì

Metodo di campionamento

Campione non probabilistico

Popolazione di studio

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.

Descrizione

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

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

Coorti e interventi

Gruppo / 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.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Hexagon Agility Test Completion Time
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Pubblicazioni e link utili

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Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

1 aprile 2026

Completamento primario (Stimato)

31 gennaio 2027

Completamento dello studio (Stimato)

28 febbraio 2027

Date di iscrizione allo studio

Primo inviato

26 agosto 2026

Primo inviato che soddisfa i criteri di controllo qualità

31 agosto 2026

Primo Inserito (Effettivo)

1 settembre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

1 settembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

31 agosto 2026

Ultimo verificato

1 agosto 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • CMUH115-REC3-011
  • NSTC115-2813-C-039-101-B (Altro numero di sovvenzione/finanziamento: National Science and Technology Council)

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Descrizione del piano 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.

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .