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Comparison of Combined Sprint-Plyometric Training Versus Traditional Strength Training on Speed, Agility, Power, and Movement Quality in Intermediate Rugby Players

15. maj 2026 opdateret af: Hafsah Gul Khattak, Ibadat International University, Islamabad

Comparison of Combined Sprint-Plyometric Training Versus Traditional Strength Training on Speed, Agility, Power, and Movement Quality in Intermediate Rugby Players: A Randomized Controlled Trial

Comparison of Combined Sprint-Plyometric Training Versus Traditional Strength Training on Speed, Agility, Power, and Movement Quality in Intermediate Rugby Players: A Randomized Controlled Trial

Studieoversigt

Detaljeret beskrivelse

This randomized controlled trial compares combined sprint-plyometric training (Group A) versus traditional strength training (Group B) in 64 intermediate-level rugby players (aged 18-25 years). Both interventions are delivered over 8 weeks at 2 sessions per week. Primary and secondary outcomes include speed (40 m and 80 m sprint via electronic timing gates), agility (T-Test), lower-body explosive power (Standing Long Jump), and movement quality (Functional Movement Screen), assessed at baseline and post-intervention. Randomization is performed via computer-generated sequence.

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

64

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Studiesteder

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

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen

Tager imod sunde frivillige

Ja

Beskrivelse

Inclusion Criteria:

  1. Male and female athletes aged 18-25 years
  2. A minimum of 2 years of structured rugby training experience
  3. Actively training at least 3 hours per week
  4. Medically cleared to engage in high-intensity physical activity
  5. Willingness to participate and provide written informed consent

Exclusion Criteria:

  1. History of moderate or severe musculoskeletal injuries or surgery within the past 6-12 months
  2. Not medically approved to engage in high-intensity physical activities
  3. Cardiovascular or cardiopulmonary disease or risk factors that contraindicate high-intensity training
  4. Participation in any additional structured strength or plyometric program outside the study protocol during the intervention period

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Enkelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Combined Sprint-Plyometric Training Group
Participants perform progressive sprint (10-100 m) and plyometric exercises (squat jumps, box jumps, single-leg hops, depth jumps) over 8 weeks. Frequency: 2 sessions/week, 45-60 min/session. Rest between sets: 3 minutes. Rest between sessions: 48-72 hours. Volume and distance progress across 4 two-week blocks.
Participants perform progressive sprint (10-100 m) and plyometric exercises (squat jumps, box jumps, single-leg hops, depth jumps) over 8 weeks. Frequency: 2 sessions/week, 45-60 min/session. Rest between sets: 3 minutes. Rest between sessions: 48-72 hours. Volume and distance progress across 4 two-week blocks
Aktiv komparator: Traditional Strength Training Group
Participants perform lower-body resistance exercises (barbell squat, leg press, lunges, Romanian deadlift, leg curl, leg extension) at 60-80% 1RM over 8 weeks. Frequency: 2 sessions/week, 45-60 min/session. Rest between sets: 1.5-3 minutes. Load progressively increased across 4 two-week blocks
Participants perform lower-body resistance exercises (barbell squat, leg press, lunges, Romanian deadlift, leg curl, leg extension) at 60-80% 1RM over 8 weeks. Frequency: 2 sessions/week, 45-60 min/session. Rest between sets: 1.5-3 minutes. Load progressively increased across 4 two-week blocks.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Sprint Speed - Electronic Timing Gates (40 m and 80 m)
Tidsramme: Baseline (Week 0) and Post-intervention (Week 8)
Sprint time measured in seconds over 40 m and 80 m distances using electronic timing gates. Very high criterion validity (r ≈ 0.95-0.99) and excellent test-retest reliability (ICC ≈ 0.90-0.99)
Baseline (Week 0) and Post-intervention (Week 8)

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Agility - T-Test
Tidsramme: Baseline (Week 0) and Post-intervention (Week 8)
Time (seconds) to complete the standard agility T-Test course assessing change-of-direction speed. High construct and criterion validity (r ≈ 0.80-0.96); high test-retest reliability (ICC ≈ 0.88-0.98)
Baseline (Week 0) and Post-intervention (Week 8)
Lower-Body Explosive Power - Standing Long Jump Test
Tidsramme: Baseline (Week 0) and Post-intervention (Week 8)
Distance (cm) achieved in the standing long jump as a measure of lower-body explosive power. Strong concurrent validity with force-plate measures (r ≈ 0.76-0.91); excellent reliability (ICC ≈ 0.97-0.99)
Baseline (Week 0) and Post-intervention (Week 8)
Movement Quality - Functional Movement Screen (FMS)
Tidsramme: Baseline (Week 0) and Post-intervention (Week 8)
Composite FMS score (0-21) assessing fundamental movement quality across 7 movement patterns. Moderate to good construct validity (r ≈ 0.60-0.85); moderate to excellent inter- and intra-rater reliability (ICC ≈ 0.74-0.98)
Baseline (Week 0) and Post-intervention (Week 8)

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Efterforskere

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

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

1. april 2026

Primær færdiggørelse (Anslået)

1. juli 2026

Studieafslutning (Anslået)

1. juli 2026

Datoer for studieregistrering

Først indsendt

9. maj 2026

Først indsendt, der opfyldte QC-kriterier

15. maj 2026

Først opslået (Faktiske)

18. maj 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

18. maj 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

15. maj 2026

Sidst verificeret

1. maj 2026

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • IIUI/RERC/ADT/2026/04/285

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