NCT07591675

Brief Summary

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

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
64

participants targeted

Target at P50-P75 for not_applicable

Timeline
1mo left

Started Apr 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress57%
Apr 2026Jul 2026

Study Start

First participant enrolled

April 1, 2026

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

May 9, 2026

Completed
9 days until next milestone

First Posted

Study publicly available on registry

May 18, 2026

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2026

Last Updated

May 18, 2026

Status Verified

May 1, 2026

Enrollment Period

3 months

First QC Date

May 9, 2026

Last Update Submit

May 15, 2026

Conditions

Keywords

Sprint trainingPlyometric trainingAgilityPower

Outcome Measures

Primary Outcomes (1)

  • Sprint Speed - Electronic Timing Gates (40 m and 80 m)

    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)

Secondary Outcomes (3)

  • Agility - T-Test

    Baseline (Week 0) and Post-intervention (Week 8)

  • Lower-Body Explosive Power - Standing Long Jump Test

    Baseline (Week 0) and Post-intervention (Week 8)

  • Movement Quality - Functional Movement Screen (FMS)

    Baseline (Week 0) and Post-intervention (Week 8)

Study Arms (2)

Combined Sprint-Plyometric Training Group

EXPERIMENTAL

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.

Other: Combined Sprint-Plyometric Training

Traditional Strength Training Group

ACTIVE COMPARATOR

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

Other: Traditional Strength Training Group

Interventions

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

Combined Sprint-Plyometric 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.

Traditional Strength Training Group

Eligibility Criteria

Age18 Years - 25 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ibadat International University, Islamabad (Iiui)

Islamabad, 46000, Pakistan

RECRUITING

Study Officials

  • Hafsah Gul Khattak, DPT, MS-NMPT

    IBADAT INTERNATIONAL UNIVERSITY, ISLAMABAD (IIUI)

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Munazza Ahmed, MS Sports Physical Therapy

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Masking Details
The outcome assessor is blinded to group allocation. Participants and the treating physiotherapist/coach are not blinded due to the nature of the intervention.
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Parallel Assignment
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

May 9, 2026

First Posted

May 18, 2026

Study Start

April 1, 2026

Primary Completion (Estimated)

July 1, 2026

Study Completion (Estimated)

July 1, 2026

Last Updated

May 18, 2026

Record last verified: 2026-05

Data Sharing

IPD Sharing
Will not share

Locations