- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03150277
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
Intervention / Treatment
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.
Sponsor
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.
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