NCT05056792

Brief Summary

This study aims to investigate the influence of an eight-week plyometric and quadriceps strength training program on muscular strength, sprint, and functional performance in collegiate football players.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jan 2021

Geographic Reach
1 country

1 active site

Status
completed

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 30, 2021

Completed
8 months until next milestone

First Submitted

Initial submission to the registry

September 14, 2021

Completed
13 days until next milestone

First Posted

Study publicly available on registry

September 27, 2021

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 30, 2022

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 28, 2022

Completed
Last Updated

November 17, 2022

Status Verified

September 1, 2021

Enrollment Period

1.4 years

First QC Date

September 14, 2021

Last Update Submit

November 14, 2022

Conditions

Keywords

Strength Resisted sprint trainingPlyometric trainingFunction performanceResisted sprint training

Outcome Measures

Primary Outcomes (3)

  • Maximal Voluntary Isometric Contraction Strength (STN)

    Pretest and post intervention strength measure.

    After 8 weeks of intervention

  • Sprint Test (ST)

    Pretest and post intervention sprint measure.

    After 8 weeks of intervention

  • Single-Leg Triple Hop Test (SLTH)

    Pretest and post intervention single-leg triple hop measure.

    After 8 weeks of intervention

Study Arms (2)

Participants in this group will receive isometric strength training.

EXPERIMENTAL

Isometric strength training of the quadriceps femoris muscle for 8 weeks.

Other: Isometric strength training for 8 weekOther: Conventional training

Participants in this group will receive plyometric training.

SHAM COMPARATOR

Participants in this group will receive plyometric training for 8 weeks.

Other: Isometric strength training for 8 weekOther: Conventional training

Interventions

Plyometric training for 8 week

Also known as: plyometric training training
Participants in this group will receive isometric strength training.Participants in this group will receive plyometric training.

Conventional training for 8 week

Participants in this group will receive isometric strength training.Participants in this group will receive plyometric training.

Eligibility Criteria

Age18 Years - 25 Years
Sexmale(Gender-based eligibility)
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Young players aged between 18 and 25 years required frequent sprinting

You may not qualify if:

  • Current injury to the lower limb.
  • Surgery affecting lower limb function.
  • Any cardio-respiratory diseases.
  • Impairments of the spine or lower extremities.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Physiotherapy and Rehabilitation center

Al Majma'ah, Riyadh Region, 11952, Saudi Arabia

Location

MeSH Terms

Interventions

Plyometric Exercise

Intervention Hierarchy (Ancestors)

Exercise TherapyRehabilitationAftercareContinuity of Patient CarePatient CareTherapeuticsPhysical Therapy ModalitiesPhysical Conditioning, HumanExerciseMotor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Officials

  • Shahnaz Hasan, PhD

    Majmaah University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, CARE PROVIDER
Masking Details
Randomized
Purpose
PREVENTION
Intervention Model
PARALLEL
Model Details: Randomized controlled trial
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

September 14, 2021

First Posted

September 27, 2021

Study Start

January 30, 2021

Primary Completion

June 30, 2022

Study Completion

August 28, 2022

Last Updated

November 17, 2022

Record last verified: 2021-09

Data Sharing

IPD Sharing
Will not share

Data has been kept secure with the principal investigator Dr. Shahnaz Hasan due to confidentiality issues.

Locations