- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07458373
Effects of Plyometric Versus Resistance Band Training on Agility and Rate of Perceived Exertion Among Recreational Football Players
Effects of Plyometric Versus Resistance Band Training on Agility and Rate of Perceived Exertion Among Recreational Football Players: A Randomized Clinical Trial
The goal of the current study is to evaluate the plyometrics and resistance band training in recreational football players, aged 18-25 years. The main question it aims to answer are:
Does the plyometrics significantly improve agility and reduce Rate of Perceived Exertion (RPE)? Does the resistance band training significantly improve agility and reduce RPE? Participants will be assigned to either an experimental group receiving plyometrics or arm comparator group receiving resistance band training, and will complete standardized assessment of agility and RPE before and after the intervention.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Sabeen Sabir, DPT
- Phone Number: +923235565534
- Email: sabeensabir0300@gmail.com
Study Contact Backup
- Name: MUHAMMAD TARIQ RAFIQ, PhD
- Phone Number: +923214495948
- Email: tariq.rafiq@ubas.edu.pk
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Population selected: Male recreational footballers.
- Participants who were football players had been actively participating in football academies for more than 6 months.
- Participants must be active and are in good health.
Exclusion Criteria:
- Participants with any neurological and spinal impairments, cardiopulmonary diseases and musculoskeletal disorders.
- Participants with history of any lower limb surgeries that affect lower limb function
- Participants not regularly attending the training programs.
- Participants with history of any lower limb fracture and ligament sprain.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Plyometrics with warm up and cool down exercises
|
Participants in this group will follow a 6-week program targeting the plyometric exercises with warm up and cool down exercises.
Warm up and cool down exercises are performed before and after the plyometric exercises respectively, only for 5 minutes.
Plyometrics exercises include side jumps, countermovement jumps and double bound leg jumps (3 sets X 10 repetitions, with 1 minute resting between each set, performed 4 days a week for 6 weeks) to improve agility.
The intervention aims to improve agility and reduce levels of exertion in recreational football players.
|
|
Active Comparator: Resistance band training with warm up and cool down exercises
|
Participants in this group will follow a 6-week program targeting the resistance band exercises with warm up and cool down exercises.
Warm up and cool down exercises are performed before and after resistance band exercises respectively, only for 5 minutes.
Resistance band exercises include squats, lunges, and side lunges using resistance bands (3 sets X 10 repetitions, with 1 minute resting between each set, performed 4 days a week for 6 weeks) to improve agility.
The intervention aims to improve agility and reduce levels of exertion in recreational football players.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Agility
Time Frame: From enrollment to the end of treatment at 6 weeks
|
Agility is the ability to maintain control of body position while changing direction rapidly, whether moving to the left, right, or behind the body.
Balance, coordination, strength and speed are all measured as part of agility while moving rapidly through obstacles.
Agility is a significant factor in various sports as it helps in acquiring preparedness.
Agility is assessed using the Illinois agility Test (IAT).
IAT is a timed test including a prone start position followed by a quick transition to standing and running through multidirectional obstacles.
It is a widely used tool for assessing agility by evaluating an athlete's ability to change direction and accelerate quickly within a set course, reflecting agility demands across various sports.
The change of direction agility test is reported to have high reliability and validity for team sports.
|
From enrollment to the end of treatment at 6 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Rate of Perceived Exertion
Time Frame: From enrollment to the end of treatment at 6 weeks
|
Rate of Perceived Exertion (RPE) is a subjective measure, affected by physiological and psychological factors.
It largely depends on how an athlete feels about the heaviness or lightness of a workload provided that mental state and fatigue level experienced during exercise play significant roles.
The subjective nature of RPE reflect an athlete's perceived internal effort and help us gain a more complete picture about training load.
RPE is measured by using Modified Borg Scale.
The scale ranges from 1 to 10 where 1 represents "really easy" and 10 represents "maximal; just like my hardest race".
Participants select the number that best represents their current level of exertion, with higher scores indicating maximal levels of exertion.
|
From enrollment to the end of treatment at 6 weeks
|
Collaborators and Investigators
Investigators
- Principal Investigator: Muhammad Tariq Rafiq, Lahore University of Biological & Applied Sciences
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- DPT/ERB/37
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- CSR
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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