Post - Activation Potentiation After Plyometric and Heavy Resistance Exercise in Soccer Players

June 19, 2017 updated by: Md. Shahid Raza, Jamia Millia Islamia

Post - Activation Potentiation Following Acute Bouts of Plyometric Versus Heavy Resistance Exercise in Collegiate Soccer Players

The main purpose of this study will be comparison of acute effects of plyometric and heavy resistance exercise on post-activation potentiation

Study Overview

Status

Completed

Conditions

Detailed Description

This is a single-center, randomized, crossover study. Collegiate soccer players will be enrolled in this study. The study will be performed in 3 separate sessions.In the first session, participants will be familiarized with the experimental conditions and 1RM will be calculated. Participants will then be randomized to receive either heavy resistance or plyometric exercise first in the second session and then will be crossed over to receive the opposite intervention in the third session. The objective of the study is to compare the acute effects of plyometric and heavy resistance exercise on post - activation potentiation by measuring physical performance and blood lactate level.

Study Type

Interventional

Enrollment (Actual)

14

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Delhi
      • New Delhi, Delhi, India, 110025
        • Sports Complex, Jamia Millia Islamia

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

14 years to 22 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • Collegiate soccer players aged 18 - 26 years
  • Participants must have at least 2 years of playing experience
  • Participants should be involved in sport-specific training on at least 2 occasions per week and play competitively once per week

Exclusion Criteria:

  • Lower extremity reconstructive surgery in last 24 months or unresolved musculoskeletal disorder which would prohibit subject to participate in the sport.
  • Participants who are consuming (or had consumed) growth hormone, anabolic steroids or any kind of performance enhancing drugs.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Plyometric-Resistance
This group will perform plyometric exercise first and then heavy resistance exercise
2 sets of 10 ankle hops, 3 sets of 5 hurdle hops, 5 drop-jumps from a height of 50 cm
10 single repetitions of back half squats at 90% of 1 repetition maximum
Experimental: Resistance-Plyometric
This group will perform resistance exercise first and then plyometric exercise
2 sets of 10 ankle hops, 3 sets of 5 hurdle hops, 5 drop-jumps from a height of 50 cm
10 single repetitions of back half squats at 90% of 1 repetition maximum

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Blood lactate level
Time Frame: Measured prior to and after the intervention period (at 1 minute and 10 minute)
Small pinprick blood samples will be taken from fingertip and blood lactate level will be measured by Blood lactate analyser (EKF Diagnostic Lactate Scout +, UK). The area will be cleaned first, using a dry tissue to remove sweat, then an alcohol swab. Once the area is dry, the lancet (often with a spring loaded apparatus) will be used to pierce the skin.
Measured prior to and after the intervention period (at 1 minute and 10 minute)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Countermovement jump height
Time Frame: Measured prior to and after the intervention period (at 1 minute and 10 minute)
The countermovement jump height will be measured using an iPhone app 'My Jump'. Jump height will be determined using an acknowledged flight - time calculation. During the CMJ, the subject rest their hands on their hips while performing a downward movement, followed by a maximum effort vertical jump. The subjects have to land in an upright position and to bend knees on landing.
Measured prior to and after the intervention period (at 1 minute and 10 minute)
20 m single sprint time
Time Frame: Measured prior to and after the intervention period (at 1 minute and 10 minute)
The 20m single sprint is a standard test for assessing soccer players' running speed. The test involves running a single maximum sprint over 20 meters, with the time recorded using a stopwatch.
Measured prior to and after the intervention period (at 1 minute and 10 minute)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Shahid Raza, MPT, Jamia Millia Islamia

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 13, 2017

Primary Completion (Actual)

June 7, 2017

Study Completion (Actual)

June 7, 2017

Study Registration Dates

First Submitted

May 9, 2017

First Submitted That Met QC Criteria

May 9, 2017

First Posted (Actual)

May 12, 2017

Study Record Updates

Last Update Posted (Actual)

June 20, 2017

Last Update Submitted That Met QC Criteria

June 19, 2017

Last Verified

June 1, 2017

More Information

Terms related to this study

Other Study ID Numbers

  • 4/10/95/JMI/IEC/2016

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

IPD Plan Description

Data will be kept secure with principal investigator (Md. Shahid Raza) and sub-investigator (Sourabh Kumar Sharma) due to confidentiality issues

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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.

Clinical Trials on Soccer

Clinical Trials on Plyometric exercise

Subscribe