Effects of Post-activation Performance Enhancement Protocols on Judo-specific Performance: a Randomized Crossover Trial

January 14, 2025 updated by: Universidade do Porto

Effects of Post-activation Performance Enhancement Protocols Using Upper-body, Lower-body, or Combined Upper- and Lower-body Exercises on Judo-specific Performance: a Randomized Crossover Trial

The study aimed to investigate the post-activation performance enhancement (PAPE) of the special judo fitness test (SJFT) of youth judo athletes using upper-body (isometric push-ups), lower-body (standing broad jumps), or their combination as conditioning exercise (CE).

Study Overview

Detailed Description

Fourteen females (aged 16.5 ± 0.8 yrs) and nine males (aged 17.0 ± 0.9 yrs) performed the three CEs or a control condition (i.e., judo-specific warm-up) in a randomized crossover method. The SJFT was conducted one minute after the CE or control condition.

Study Type

Interventional

Enrollment (Actual)

25

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

      • Porto, Portugal, 4200-450
        • Faculty of Sport of the University of Porto

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Minimum of 4 years of judo training and competition experience.
  • Actively practicing the sport and preparing for a competition during the time of data collection
  • Proficient at performing the ippon seoi-nage throwing (judo) technique

Exclusion Criteria:

  • Disease or serious injury that inhibited participating in the warm-up protocols and subsequent testing sessions.

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: Upper body PAPE protocol
Half of the judo-specific protocol + 3 sets of 10-second hold isometric push-ups.
Assess which intervention delivered the best acute performance enhancements.
Experimental: Lower body PAPE protocol
Half of the judo-specific protocol + 3 sets of 6 repetitions of standing broad jump.
Assess which intervention delivered the best acute performance enhancements.
Experimental: Combined (Upper body+Lower body) PAPE protocol
Half of the judo-specific protocol + 3 sets of 3 repetitions of standing broad jump + 3 sets of 5-second hold isometric push-ups.
Assess which intervention delivered the best acute performance enhancements.
Active Comparator: Control (judo-specific) protocol
Judo-specific exercises that included 10 repetitions of ukemi drills (i.e., front, back, side, and rolling), 2 sets of 10 repetitions of "rapid" uchikomi drills (i.e., throwing drills), 2 sets of 1 minute of kumikata fight (i.e., grip fight), and 2 sets of 10 repetitions of nagekomi (i.e., practice throws).
Assess which intervention delivered the best acute performance enhancements.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Special judo fitness test (SJFT)
Time Frame: 15 seconds for the 1st set, 30 seconds for sets #2 and #3
Three sets of time-limited judo throws, assessing the number of throws
15 seconds for the 1st set, 30 seconds for sets #2 and #3

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Heart rate
Time Frame: During the SJFT, immediately after the SJFT, and 1 minute after the SJFT
Monitoring of heart rate
During the SJFT, immediately after the SJFT, and 1 minute after the SJFT
Rate of perceived exertion
Time Frame: 30 minutes after each testing session
Assess perceived exertion
30 minutes after each testing session

Collaborators and Investigators

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

Investigators

  • Study Chair: José Afonso, Ph.D., Faculty of Sport of the University of Porto

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)

September 1, 2023

Primary Completion (Actual)

October 20, 2023

Study Completion (Actual)

October 20, 2023

Study Registration Dates

First Submitted

January 6, 2025

First Submitted That Met QC Criteria

January 6, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

January 14, 2025

Last Verified

January 1, 2025

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • IRB/SPES/NOC/2023-24/03

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

Anonymised data pertaining sample characteristics and results of the implemented assessments will be shared upon request.

IPD Sharing Time Frame

Anonymised data pertaining sample characteristics and results of the implemented assessments will be shared upon request. No predicted end date.

IPD Sharing Access Criteria

Anonymised data pertaining sample characteristics and results of the implemented assessments will be shared upon request.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ICF

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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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