Impact of the Wingate Test on Post-activation Potentiation

Comparing the Effects of Post Activation Potentiation on Vertical Jump Using High-Intensity Back Squat vs. Wingate Bike Test in Healthy Adults

The goal of this trial is to see if using a maximal effort, short cycling test is better at activating muscles to improve vertical jump height compared to a maximal effort back squat. The study looks to answer three questions:

  1. will the Wingate bike test create a different change in counter movement jump height compared to a back squat?
  2. What is the best recovery period after each test where the counter movement jump is the highest?
  3. What person-specific factors predict success of the Wingate bike test as a activation activity for the counter movement jump? Participants will visit the lab 3 times, once to give informed consent and measure their 1 repetition max (RM) back squat, and twice to perform each intervention and measure vertical jump height.

Study Overview

Status

Completed

Detailed Description

Participants will be asked to come to the lab for three visits. On the first visit, they will perform informed consent, have anthropometrics taken, and will provide data to assess weightlifting history and factors that may influence the impact of each intervention. They will perform a 1 repetition max (RM) test for the back squat in order to properly dose the back squat potentiation activity. Visits 2 and 3 will be randomized; one will use the back squat (control) and the other will use the Wingate bike test (experimental) to potentiate vertical jump height as measured by the counter movement jump (CMJ). In each session, a warm up will be performed and the baseline CMJ will be performed. The intervention will be performed, either the 30 second Wingate protocol which is a maximal effort cycling test, or the back squat at a high percent of the 1 RM. The CMJ will be reassessed at 3, 6, and 9 minutes after completed each intervention.

Study Type

Interventional

Enrollment (Actual)

35

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

    • Louisiana
      • Shreveport, Louisiana, United States, 71103
        • LSU Health Shreveport School of Allied Health Professions

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:

  • healthy adult
  • successful completion of the physical activity readiness questionnaire plus
  • at least 1 year of back squat weight training experience

Exclusion Criteria:

  • inability to back squat at least 1.4 times body weight
  • females with known pregnancy

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: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Back squat
Participants will perform 2 sets of 3 repetitions at 85% of their 1 repetition maximum weight for the back squat
2 sets of 3 repetitions of a back squat, set to 85% of the 1 repetition maximum weight
Experimental: Wingate test
Participants will perform the Wingate bike test, with resistance at 7.5% of body weight, with a maximal effort for 30 seconds.
30 second maximal effort cycling test, with resistance at 7.5% bodyweight

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Vertical Jump Height
Time Frame: Visit 2 (1 week post- enrollment); visit 3 (2 weeks post-enrollment)
Measured with the Counter Movement Jump (CMJ). This measures the vertical distance a participant is able to jump from a standing, stationary position. Video capture and motion analysis software will be used to analyze the jump and determine vertical displacement of a marker placed at the participants sacrum. Vertical jump height will be measured in meters.
Visit 2 (1 week post- enrollment); visit 3 (2 weeks post-enrollment)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Years of resistance training experience
Time Frame: Collected at visit 1, upon enrollment into the study
This factor will be collected to examine its predictive impact on the Wingate test's potentiation effect. The number of years of resistance training each participants has participated in will be collected.
Collected at visit 1, upon enrollment into the study
One-Repetition Maximum Back Squat Strength
Time Frame: Collected at visit 1, upon enrollment into the study
This factor will be collected to examine its predictive impact on the Wingate test's potentiation effect. The 1 repetition maximum weight in kilograms for the back squat exercise will be collected.
Collected at visit 1, upon enrollment into the study

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Erin McCallister, DPT, Louisiana State University Health Sciences Center Shreveport

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)

January 14, 2025

Primary Completion (Actual)

April 25, 2025

Study Completion (Actual)

April 25, 2025

Study Registration Dates

First Submitted

January 6, 2025

First Submitted That Met QC Criteria

January 10, 2025

First Posted (Actual)

January 16, 2025

Study Record Updates

Last Update Posted (Actual)

July 4, 2025

Last Update Submitted That Met QC Criteria

July 1, 2025

Last Verified

March 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

All of the individual participant data collected during the trial, after deidentification.

IPD Sharing Time Frame

Available 3 months following publication of findings, no end date (link to be provided)

IPD Sharing Access Criteria

Researchers wishing to access the data

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL

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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