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Acute Effects of Bilateral Versus Unilateral Isometric Conditioning Activity on Jump Performance in Volleyball Players (BI-UNI ICA)

Acute Effects of Bilateral Versus Unilateral Isometric Conditioning Activity on Bilateral and Unilateral Jump Performance in Highly Trained Male Volleyball Players: A Randomized Crossover Trial

This randomized crossover trial investigates the acute effects of bilateral and unilateral isometric conditioning activity on bilateral and unilateral jump performance in highly trained male volleyball players. Fourteen athletes will complete three experimental conditions in randomized order: bilateral isometric squat conditioning activity (BI), unilateral isometric squat conditioning activity (UNI), and a control condition consisting of low-intensity treadmill walking (CTRL). In both isometric conditions, participants will perform three sets of three maximal 3-second contractions, with 3-minute recovery intervals between sets. Jump performance will be assessed before each experimental condition and at 4, 8, and 12 minutes afterward using bilateral countermovement jumps and single-leg jumps performed separately with each lower limb. The primary aim of the study is to determine whether the mode of isometric conditioning activity, unilateral versus bilateral, influences the magnitude and time course of acute changes in jump performance. An additional objective is to assess whether the effects of the conditioning activity differ between bilateral and unilateral jumping tasks.

Studienübersicht

Detaillierte Beschreibung

This study is a randomized, counterbalanced crossover trial designed to examine the acute effects of unilateral and bilateral isometric conditioning activity on jump performance in highly trained male volleyball players. Fourteen participants will complete three experimental conditions on separate occasions in randomized order: bilateral isometric conditioning activity (BI), unilateral isometric conditioning activity (UNI), and a control condition (CTRL). Because each participant will complete all three conditions, every athlete will serve as his own control.

Each experimental session will begin with a standardized warm-up consisting of 5 minutes of cycling followed by bodyweight squats, walking lunges, thoracic spine rotations, and submaximal countermovement jumps. Baseline jump performance will then be assessed using two bilateral countermovement jumps and two single-leg jumps performed separately with each lower limb. The single-leg jump will involve take-off from one limb and landing on both limbs.

In the BI condition, participants will perform three sets of three maximal 3-second bilateral isometric squat contractions against an immovable resistance, with 3-minute recovery intervals between sets. In the UNI condition, participants will perform three sets of three maximal 3-second unilateral isometric squat contractions with each lower limb. The limbs will be alternated to reduce systematic differences in recovery time between sides. In the CTRL condition, participants will complete 9 minutes of low-intensity treadmill walking at 6 km/h.

Following each experimental condition, bilateral countermovement jump and single-leg jump performance will be reassessed at 4, 8, and 12 minutes. All jumps will be performed on force platforms. The primary outcome will be bilateral countermovement jump height. Secondary outcomes will include single-leg jump height and selected force-time variables derived from the bilateral and unilateral jump tests.

The primary objective of the study is to compare the acute effects of unilateral and bilateral isometric conditioning activity on bilateral countermovement jump performance. A secondary objective is to determine whether the type of conditioning activity produces task-specific effects on unilateral jump performance and whether the time course of post-activation performance enhancement differs between the BI and UNI conditions.

Studientyp

Interventionell

Einschreibung (Geschätzt)

14

Phase

  • Unzutreffend

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

    • Silesian Voivodeship
      • Katowice, Silesian Voivodeship, Polen, 40-065
        • Academy of Physical Education in Katowice

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Kind
  • Erwachsene
  • Älterer Erwachsener

Akzeptiert gesunde Freiwillige

Ja

Beschreibung

Inclusion Criteria:

  • minimum of 7 years of systematic volleyball training,
  • at least 3 resistance training sessions per week during the preceding 5 years,
  • no musculoskeletal injury requiring training cessation longer than 4 weeks within 6 months prior to enrollment,
  • absence of tattoos over the rectus femoris muscle that could interfere with thermographic assessment.

Exclusion Criteria:

  • less than 7 years of systematic volleyball training,
  • less than 3 resistance training sessions per week during the previous 5 years,
  • any musculoskeletal injury within the 6 months prior to enrollment that required cessation of training for longer than 4 weeks,
  • current musculoskeletal pain or injury that could affect jumping performance or participation in maximal isometric exercise,
  • tattoos, scars, or skin conditions over the rectus femoris muscle that could interfere with thermographic measurements,
  • use of medications or substances that may affect neuromuscular performance or muscle function,
  • failure to comply with study procedures or testing requirements.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Grundlegende Wissenschaft
  • Zuteilung: Zufällig
  • Interventionsmodell: Crossover-Aufgabe
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Bilateral Isometric Conditioning Activity
Participants will perform a bilateral isometric conditioning activity consisting of three sets of three maximal 3-second isometric squat contractions against an immovable resistance. Each set will be separated by 3 minutes of recovery.
Three sets of three maximal 3-second bilateral isometric squat contractions performed against an immovable resistance, with 3-minute recovery intervals between sets. Participants will be instructed to push as hard and as fast as possible during each contraction.
Andere Namen:
  • BI
Experimental: Unilateral Isometric Conditioning Activity
Participants will perform a unilateral isometric conditioning activity consisting of three sets of three maximal 3-second isometric squat contractions with each lower limb against an immovable resistance. The lower limbs will be alternated, and each set will be separated by 3 minutes of recovery.
Three sets of three maximal 3-second unilateral isometric squat contractions performed with each lower limb against an immovable resistance. The lower limbs will be alternated, and 3-minute recovery intervals will be provided between sets. Participants will be instructed to push as hard and as fast as possible during each contraction.
Andere Namen:
  • UNI
Experimental: Control Condition
Participants will complete 9 minutes of low-intensity treadmill walking at a speed of 6 km/h. This condition will serve as the control condition for comparison with the bilateral and unilateral isometric conditioning activities.
All participants will complete all three experimental conditions in a randomized and counterbalanced order, with a standardized recovery interval between sessions. Each participant will therefore serve as his own control.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Changes in Bilateral Countermovement Jump Height
Zeitfenster: Baseline and 4, 8, and 12 minutes after each experimental condition
Bilateral countermovement jump height will be assessed using dual force platforms operating at a sampling frequency of 1000 Hz. Jump height will be calculated from center-of-mass take-off velocity using the impulse-momentum method and expressed in centimeters. Participants will perform two valid trials at each time point, and the mean value will be used for analysis. Changes from the condition-specific baseline will be compared between the bilateral isometric, unilateral isometric, and control conditions.
Baseline and 4, 8, and 12 minutes after each experimental condition
Changes in Single-Leg Jump Height
Zeitfenster: Baseline and 4, 8, and 12 minutes after each experimental condition
Single-leg jump height will be assessed separately for the right and left lower limbs using force platforms. Each jump will be performed with take-off from one limb and landing on both limbs. Jump height will be calculated from center-of-mass take-off velocity using the impulse-momentum method and expressed in centimeters. Two valid trials will be performed with each limb at each time point, and the mean value for each limb will be used for analysis.
Baseline and 4, 8, and 12 minutes after each experimental condition

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Changes in Bilateral Countermovement Jump Modified Reactive Strength Index
Zeitfenster: Baseline and 4, 8, and 12 minutes after each experimental condition
The modified reactive strength index during the bilateral countermovement jump will be calculated as jump height in meters divided by time to take-off in seconds and expressed in meters per second. Participants will perform two valid trials at each time point, and the mean value will be used for analysis.
Baseline and 4, 8, and 12 minutes after each experimental condition
Changes in Inter-Limb Concentric Impulse Asymmetry During the Bilateral Countermovement Jump
Zeitfenster: Baseline and 4, 8, and 12 minutes after each experimental condition
Concentric impulse will be calculated separately for the right and left lower limbs from force-time data recorded using dual force platforms. Inter-limb asymmetry will be expressed as a percentage and calculated using the following formula: absolute difference between limbs divided by the higher limb value, multiplied by 100. A value of 0% represents perfect symmetry, while higher values indicate greater inter-limb asymmetry. The mean of two valid trials will be used for analysis.
Baseline and 4, 8, and 12 minutes after each experimental condition
Changes in Inter-Limb Single-Leg Jump Height Asymmetry
Zeitfenster: Baseline and 4, 8, and 12 minutes after each experimental condition
Inter-limb asymmetry in single-leg jump height will be calculated from the mean jump height obtained separately for the right and left lower limbs. Asymmetry will be expressed as a percentage and calculated as the absolute difference between limbs divided by the higher limb value, multiplied by 100. A value of 0% represents perfect symmetry, while higher values indicate greater inter-limb asymmetry.
Baseline and 4, 8, and 12 minutes after each experimental condition

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Publikationen und hilfreiche Links

Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

23. Juli 2026

Primärer Abschluss (Geschätzt)

3. August 2026

Studienabschluss (Geschätzt)

3. August 2026

Studienanmeldedaten

Zuerst eingereicht

13. Juli 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

13. Juli 2026

Zuerst gepostet (Tatsächlich)

16. Juli 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

16. Juli 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

13. Juli 2026

Zuletzt verifiziert

1. Juli 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

JA

Beschreibung des IPD-Plans

De-identified individual participant data will be shared upon reasonable request after publication of the study results. Requests should be directed to the corresponding author.

IPD-Sharing-Zeitrahmen

De-identified individual participant data and supporting documents will be available beginning 3 months after publication of the primary study results and will remain available for 5 years.

IPD-Sharing-Zugriffskriterien

De-identified individual participant data and supporting documents will be made available to qualified researchers who submit a methodologically sound research proposal. Requests should be directed to the corresponding author and will be reviewed by the study investigators. Access will be granted for analyses consistent with the approved proposal and may require a data-use agreement.

Art der unterstützenden IPD-Freigabeinformationen

  • STUDIENPROTOKOLL
  • SAFT

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

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