Diese Seite wurde automatisch übersetzt und die Genauigkeit der Übersetzung wird nicht garantiert. Bitte wende dich an die englische Version für einen Quelltext.

Effect of Upper-limb Plyometric Training Versus Strength Training for Enhancing Serve Velocity, Strength, and Power in Competitive Tennis Players (ULPT-ST)

24. Juni 2026 aktualisiert von: Hafsah Gul Khattak, Ibadat International University, Islamabad

This study aims to compare the effects of upper-limb plyometric training and traditional strength training on serve velocity, muscular strength, and power in competitive tennis players. Serve velocity is a critical performance factor in tennis, and optimizing upper-limb function is essential for enhancing performance.

Participants will be randomly assigned to either a plyometric training group or a strength training group. Both groups will undergo structured training programs over a defined intervention period. Outcome measures, including serve velocity, upper-limb strength, and power, will be assessed at baseline and after the completion of the intervention.

The findings of this study will help determine the most effective training approach for improving performance in tennis players and may guide coaches, athletes, and rehabilitation professionals in designing evidence-based training programs.

Studienübersicht

Detaillierte Beschreibung

Tennis performance is highly dependent on the ability to generate force, speed, and coordination, particularly during the serve. Upper-limb strength and power play a crucial role in producing high serve velocity, which is a key determinant of competitive success. Various training approaches have been used to enhance these physical attributes, including traditional resistance training and plyometric training.

Plyometric training focuses on explosive movements that utilize the stretch-shortening cycle, potentially improving neuromuscular efficiency and power output. In contrast, traditional strength training emphasizes muscle force production through controlled resistance exercises. While both approaches are widely used, there is limited comparative evidence regarding their effectiveness in improving tennis-specific performance, particularly serve velocity.

This randomized controlled trial aims to compare the effects of upper-limb plyometric training and strength training on serve velocity, muscular strength, and power in competitive tennis players. Participants will be randomly allocated into two groups: a plyometric training group and a strength training group. Each group will follow a structured training program for a specified duration under supervised conditions.

Outcome measures will include serve velocity (measured using a radar gun or equivalent device), upper-limb muscular strength (assessed through standardized strength tests), and power (evaluated using validated performance tests). Assessments will be conducted at baseline and after completion of the intervention.

Studientyp

Interventionell

Einschreibung (Geschätzt)

46

Phase

  • Unzutreffend

Kontakte und Standorte

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

Studienkontakt

Studieren Sie die Kontaktsicherung

Studienorte

      • Islamabad, Pakistan, 46000
        • Rekrutierung
        • Ibadat International University, Islamabad (Iiui)
        • Kontakt:

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

  • Erwachsene

Akzeptiert gesunde Freiwillige

Ja

Beschreibung

Inclusion Criteria:

  • Age 18-30 years (male tennis players).
  • Currently training/competing in tennis ≥3 sessions/week.
  • Minimum of 4 years of systematic tennis training experience
  • Provide written informed consent.

Exclusion Criteria:

  • Recent musculoskeletal surgery
  • Upper-limb (shoulder/elbow) or lower-limb injury that limits training in past 6 months.
  • Participation in structured strength or agility programs outside routine tennis training
  • Neurological or cardiovascular disorders or other medical condition contraindicating high-intensity exercise

Studienplan

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

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Single

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Upper-Limb Plyometric Training Group
Participants in this group will undergo an upper-limb plyometric training program designed to improve explosive strength and power. The program will include exercises such as medicine ball throws, plyometric push-ups, and overhead throws. Training sessions will be conducted three times per week for six weeks under supervision, with progressive intensity based on participant performance.
A supervised upper-limb plyometric training program designed to enhance explosive power through stretch-shortening cycle activities. The intervention includes medicine ball throws, plyometric push-ups, and reactive upper-limb drills performed with progressive intensity over 8 weeks. The program targets rapid force production and neuromuscular coordination relevant to tennis serve performance.
Aktiver Komparator: Upper-Limb Strength Training Group
Participants in this group will perform a traditional upper-limb strength training program aimed at improving muscular strength. The program will include resistance exercises such as bench press, shoulder press, and resistance band training. Sessions will be conducted three times per week for six weeks under supervision, with progressive overload applied throughout the intervention period.
A supervised upper-limb resistance training program aimed at improving maximal muscle strength and stability. The intervention includes structured resistance exercises targeting the shoulder, arm, and scapular muscles with progressive overload over 8 weeks. The program focuses on controlled force production to support tennis-specific performance.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Chest Medicine Ball Throw
Zeitfenster: Baseline and after 8 weeks of intervention
The seated chest medicine ball throw (SMBT) will be used to assess upper limb explosive power following standardized protocols from previous research. Participants sat with their back supported and feet flat on the floor, then performed maximal effort chest pass throws using a medicine ball (3 kg). After a warm up, each participant completed two to three trials with 1-2 minutes of rest, the distance from the chest to the first point of ball contact will be measured in meters; the longest throw or the mean of the best trials was recorded as the upper limb power score.
Baseline and after 8 weeks of intervention
Serve Velocity
Zeitfenster: Baseline and after 8 weeks of intervention

Serve velocity will be measured using a handheld sports radar gun positioned approximately 2-3 meters behind the baseline and aligned with the ball's flight path to minimize measurement error. Following a standardized warm-up protocol, each participant will perform 5-10 maximal-effort flat serves from the deuce court using the dominant arm. Only serves landing within the service box will be considered valid. Adequate rest intervals will be provided between trials to minimize fatigue effects.

The radar gun will record peak ball velocity immediately after ball release. The mean of the best three valid serves will be used for statistical analysis.

Baseline and after 8 weeks of intervention
1 Repetition Maximum
Zeitfenster: Baseline and after 8 weeks of intervention

Upper-limb muscular strength will be assessed using the one-repetition maximum (1RM) bench press test. Participants will perform a standardized general warm-up followed by specific warm-up sets at 50%, 70%, and 85% of their estimated 1RM.

The test will begin with a load close to the estimated 1RM, and participants will attempt to lift the weight once using correct technique. If successful, the load will be progressively increased, with 3-5 minutes of rest between attempts, until the participant fails to complete a successful lift with proper form. The highest weight successfully lifted will be recorded as the 1RM and used as the measure of maximal upper-limb strength.

Baseline and after 8 weeks of intervention

Mitarbeiter und Ermittler

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

Ermittler

  • Hauptermittler: Hafsah Gul Khattak, DPT, MS-NMPT, Ibadat International University, Islamabad (Iiui)

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 (Tatsächlich)

15. Mai 2026

Primärer Abschluss (Geschätzt)

10. Juli 2026

Studienabschluss (Geschätzt)

20. Juli 2026

Studienanmeldedaten

Zuerst eingereicht

6. Mai 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

6. Mai 2026

Zuerst gepostet (Tatsächlich)

13. Mai 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

26. Juni 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

24. Juni 2026

Zuletzt verifiziert

1. April 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Andere Studien-ID-Nummern

  • IIUI/RERC/ADT/2026/04/283

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

NEIN

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

Abonnieren