Comparison of Combined Sprint-Plyometric Training Versus Traditional Strength Training on Speed, Agility, Power, and Movement Quality in Intermediate Rugby Players
1 other identifier
interventional
64
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Apr 2026
Shorter than P25 for not_applicable
1 active site
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 Start
First participant enrolled
April 1, 2026
CompletedFirst Submitted
Initial submission to the registry
May 9, 2026
CompletedFirst Posted
Study publicly available on registry
May 18, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
July 1, 2026
May 18, 2026
May 1, 2026
3 months
May 9, 2026
May 15, 2026
Conditions
Keywords
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
EXPERIMENTALParticipants 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.
Traditional Strength Training Group
ACTIVE COMPARATORParticipants 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
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
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.
Eligibility Criteria
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
Study Officials
- PRINCIPAL INVESTIGATOR
Hafsah Gul Khattak, DPT, MS-NMPT
IBADAT INTERNATIONAL UNIVERSITY, ISLAMABAD (IIUI)
Central Study Contacts
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
- 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