Effect of PAP on Lower Limb Explosive Force in Basketball Players in CHINA

October 8, 2023 updated by: Jiazhe Li, Universiti Putra Malaysia

The Effect of Post-activation Potentiation on Lower Limb Explosive Force in Collegiate Male Basketball Players in China

The phenomenon that high-intensity warm-up activities help improve muscle strength and explosive performance is called post-activation potentiation (PAP), which is a warm-up method that uses high-intensity stimulation to induce the activation of more type II muscle fibers. However, the results of studies exploring the enhancing effect of PAP on lower limb explosive strength are still controversial. In studies with no significant difference, it is believed that there are many factors that affect PAP, such as activation method, activation intensity, recovery time and individual factors, etc., and it is difficult to control during implementation. In addition, traditional warm-up methods such as jogging and stretching have been shown to have limited effectiveness in improving athletes' performance. In the past, there have been many studies on the combination of PAP and lower limb explosive strength, but there are almost no studies on the long-term effects of PAP on the lower limb explosive strength of basketball players. Therefore, this study studies the characteristics of PAP in order to find the best activation scheme for PAP, and then combines the enhancement effect of PAP with the explosive power of the lower limbs to improve the explosive power of the lower limbs of basketball players, and verifies the long-term effect of combining PAP with explosive power training. In order to provide new changes and breakthroughs in the design of physical training for basketball players and improve the sports performance of college male basketball players.

Study Overview

Detailed Description

The study was a four-groups randomized controlled trial. In the study, the experimental group conducted a 12-week post-activation potentiation combined with lower limb explosive training intervention designed in this study. In contrast, the control group also underwent a 12-week lower limb explosive training intervention, but the warm-up method was conventional warm-up activities. Subjects participated in training intervention programs twice weekly. After the 12-week training program, data collection was completed.

  1. Warm-up content: The experimental group used PAP as a warm-up method and performed pre-stimulation to induce post-activation potentiation. The pre-activation method is back squats. The pre-activation intensity and frequency are 70% 1RM (One-Repetition Maximum) × 3, 80% 1RM × 2, 90% 1RM × 1 respectively, and the interval time is 2 minutes. The control group performed routine warm-up activities.
  2. Explosive strength training content for lower limbs: After completing the warm-up activities, there was a six-minute interval, and then the experimental group and the control group began the same explosive training content of the lower limbs.

Study Type

Interventional

Enrollment (Estimated)

48

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 Contact

  • Name: Soh kim Geok, Professor
  • Phone Number: 03-97698153
  • Email: kims@upm.edu.my

Study Contact Backup

Study Locations

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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • The population must be collegiate male basketball players and between the ages of 18 and 22;
  • Contestants must be in good health, and must have a physical training background;
  • Only students who can complete these training requirements can be included in the research data.

Exclusion Criteria:

  • Collegiate female basketball players should be excluded from this study;
  • Players with less than one year of physical training experience;
  • Participants were not healthy collegiate male basketball players such as injured players, mental patient or special students who were seriously depressed, sub-health;
  • Students who are consistently late or absent from training sessions will eventually be excluded.

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: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: PAP induced at an intensity of 70% 1RM(One-Repetition Maximum)combined with complex training
PAP induced at an intensity of 70% 1RM combined with complex training was shown over the 12 weeks.
This group of subjects first performed 3 sets of 70% 1RM squats after a routine warm-up, 3 times per set, with an interval of 2 minutes between sets. The entire process was maintained for 30 minutes, and then after a 6-minute rest, they performed complex training consists of maximum strength training (back squats) and plyometric training (drop Jump). The Intensity & Repetition of back squats is 80% 1RM × 4, 4 sets, interval time is 2min; rest for 3 minutes. , perform drop jump, intensity & repetition is 50cm (height) × 10, 4 sets, and the rest time is 2 minutes. Intervention training was conducted twice weekly for 12 weeks,and the intensity is gradually increasing over the 12 weeks.
Experimental: PAP induced at an intensity of 80% 1RM combined with complex training
PAP induced at an intensity of 80% 1RM combined with complex training was shown over the 12 weeks.
This group of subjects first performed 3 sets of 80% 1RM squats after a routine warm-up, 2 times per set, with an interval of 2 minutes between sets. The entire process was maintained for 30 minutes, and then after a 6-minute rest, they performed complex training consists of maximum strength training (back squats) and plyometric training (drop Jump). The Intensity & Repetition of back squats is 80% 1RM × 4, 4 sets, interval time is 2min; rest for 3 minutes. , perform drop jump, intensity & repetition is 50cm (height) × 10, 4 sets, and the rest time is 2 minutes. Intervention training was conducted twice weekly for 12 weeks,and the intensity is gradually increasing over the 12 weeks.
Experimental: PAP induced at an intensity of 90% 1RM combined with complex training
PAP induced at an intensity of 90% 1RM combined with complex training was shown over the 12 weeks.
This group of subjects first performed 3 sets of 90% 1RM squats after a routine warm-up, 1 times per set, with an interval of 2 minutes between sets. The entire process was maintained for 30 minutes, and then after a 6-minute rest, they performed complex training consists of maximum strength training (back squats) and plyometric training (drop Jump). The Intensity & Repetition of back squats is 80% 1RM × 4, 4 sets, interval time is 2min; rest for 3 minutes. , perform drop jump, intensity & repetition is 50cm (height) × 10, 4 sets, and the rest time is 2 minutes. Intervention training was conducted twice weekly for 12 weeks,and the intensity is gradually increasing over the 12 weeks.
Active Comparator: Routine warm-up combined with complex training
Routine warm-up combined with complex training was shown over the 12 weeks.
This group of subjects first completed a 30-minute routine warm-up, then rested for 6 minutes, and then performed complex training consisted of maximum strength training (back squats) and plyometric training (drop jump). Back squat intensity & repetition is 80% 1RM × 4, 4 sets, with an interval of 2 minutes; after resting for 3 minutes, perform a drop jump, Intensity & Repetition is 50cm (height) × 10, 4 sets, with an interval of 2 minutes. Intervention training was conducted twice weekly for 12 weeks, and the intensity was gradually increasing over the 12 weeks.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Counter Movement Jump performance of subjects (height)
Time Frame: Pre-test: Before experiment; Post-test: 12 weeks end.
This indicator is used to test the explosive force of the lower body. And by measuring it, we can get its jump height, Rate of Force Development, the Peak Rate Force Development, Peak Power, the Peak Ground Vertical Reaction Force, which are used to analyze the changes in the explosive force of the lower limbs in detail.
Pre-test: Before experiment; Post-test: 12 weeks end.
Drop Jump performance of subjects (height)
Time Frame: Pretest: Before experiment; Post-test: 12 weeks end.
This indicator is used to test the explosive force of the lower body. And by measuring it, we can get its jump height, Rate of Force Development, the Peak Rate Force Development, Peak Power, the Peak Ground Vertical Reaction Force, which are used to analyze the changes in the explosive force of the lower limbs in detail.
Pretest: Before experiment; Post-test: 12 weeks end.
Squat Jump performance of subjects (height)
Time Frame: Pre-test: Before experiment; Post-test: 12 weeks end.
This indicator is used to test the explosive force of the lower body. And by measuring it, we can get its jump height, Rate of Force Development, the Peak Rate Force Development, Peak Power, the Peak Ground Vertical Reaction Force, which are used to analyze the changes in the explosive force of the lower limbs in detail.
Pre-test: Before experiment; Post-test: 12 weeks end.
Run-up right-foot take-off, Run-up left-foot take-off performance of subjects(height)
Time Frame: Pre-test: Before experiment; Post-test: 12 weeks end.
This indicator is used to test the explosive force of the lower body. And by measuring it, we can get its jump height, Rate of Force Development, the Peak Rate Force Development, Peak Power, the Peak Ground Vertical Reaction Force, which are used to analyze the changes in the explosive force of the lower limbs in detail.
Pre-test: Before experiment; Post-test: 12 weeks end.
30-meter sprint performance of subjects(time)
Time Frame: Pre-test: Before experiment; Post-test: 12 weeks end.
By testing the subject's 30-meter sprint time, changes in the explosive power of the lower limbs can be observed.
Pre-test: Before experiment; Post-test: 12 weeks end.

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Jiazhe Li, PhD, Universiti Putra Malaysia

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)

September 15, 2023

Primary Completion (Estimated)

January 20, 2024

Study Completion (Estimated)

February 15, 2024

Study Registration Dates

First Submitted

October 2, 2023

First Submitted That Met QC Criteria

October 8, 2023

First Posted (Actual)

October 16, 2023

Study Record Updates

Last Update Posted (Actual)

October 16, 2023

Last Update Submitted That Met QC Criteria

October 8, 2023

Last Verified

October 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Since this is my doctoral thesis experiment, I won't share it until I graduate.

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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