- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05987046
Contrast Training, Post-activation Countermovement Jump Performance in High Strength Male
The Effects of Three Contrast Training Sessions in a Week on Post-activation Countermovement Jump Performance in High Strength Male
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Previous researches indicated that the primary contributor of contrast training to improving explosive performance might be the phenomenon of post-activation performance enhancement (PAPE), with emphasis on conducting plyometric training at the optimal PAPE time. However, the PAPE appeared to be susceptible to fatigue and delayed potentiation of neuromuscular performance. Thus, its applicability in practical training is not yet clarified. The purposes of this study are to: 1) examine the effects of three contrast training sessions in a week on individual and group's PAPE and the optimal timepoint of PAPE; 2) assess the intrasession and intersession reliability of the optimal PAPE timepoints of both individuals and groups; 3) determine the relationship between kinematic parameters during resistance training and PAPE.
Qualified participants will visit the laboratory five times for experimental familiarization, One repetition maximum (1RM) of parallel squat test, and three contrast training sessions, with each contrast training session consisting of three sets of parallel squats in a week. Alongside this, countermovement jump tests will be conducted before the first set of squats and at 1, 3, 5, 7, 9, and 11 minutes after each squat set, with the kinematic parameters of the parallel squats also being collected.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Taoyuan, Taiwan, 33301
- National Taiwan Sport University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Least 2 years of resistance training experience.
- Least 1.75 times body weight of squat 1RM
- Currently engaged in regular exercise training.
Exclusion Criteria:
- Skeletal muscle injury within the past six months.
- Non-responders to PAPE
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Contrast training sessions
Participants will perform three contrast training sessions for a week.
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Three sets of three repetitions of parallel squats at 90% of 1RM
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
post-activation performance enhancement (PAPE)
Time Frame: Change in baseline and 1, 3, 5, 7, 9, and 11 minutes after each squat set.
|
PAPE will be evaluated by maximum height of countermovement jump in this study.
|
Change in baseline and 1, 3, 5, 7, 9, and 11 minutes after each squat set.
|
|
Within-group neuromuscular fatigue
Time Frame: Up to 2 weeks.
|
Within-group neuromuscular fatigue will be evaluated by velocity loss rate calculated from maximum and minimum concentric mean velocities of each set for squat in this study.
|
Up to 2 weeks.
|
|
Between-group neuromuscular fatigue
Time Frame: Up to 2 weeks.
|
Between-group neuromuscular fatigue will be evaluated by the fastest mean concentric velocity of each squat set in this study.
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Up to 2 weeks.
|
|
Between-day squat performance
Time Frame: Up to 2 weeks.
|
Between-day squat performance will be evaluated by the fastest mean concentric velocity of first squat set for each contrast training in this study.
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Up to 2 weeks.
|
|
Delayed potentiation of neuromuscular performance (DPNP)
Time Frame: Up to 2 weeks.
|
DPNP will be evaluated by maximum height of countermovement jump in this study.
|
Up to 2 weeks.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Weight
Time Frame: Baseline
|
Weight in kilograms.
|
Baseline
|
|
Height in meters
Time Frame: Baseline
|
Height in meters.
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Baseline
|
|
Body fat
Time Frame: Baseline
|
The body weight and fat weight will be combined to calculate the body fat in percentage.
|
Baseline
|
|
Squat 1RM
Time Frame: Baseline
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Squat 1RM will be evaluated maximum weight lifted for 1 repetition of squat in this study.
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Baseline
|
|
Concentric mean force of squat
Time Frame: Up to 2 weeks.
|
Concentric mean force in newtons.
|
Up to 2 weeks.
|
|
Concentric peak force of squat
Time Frame: Up to 2 weeks.
|
concentric peak force in newtons.
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Up to 2 weeks.
|
|
Concentric mean velocity of squat
Time Frame: Up to 2 weeks.
|
Concentric mean velocity in meters per second.
|
Up to 2 weeks.
|
|
Concentric mean velocity loss of squat
Time Frame: Up to 2 weeks.
|
Concentric mean velocity loss in percentage.
|
Up to 2 weeks.
|
|
Concentric peak velocity of squat
Time Frame: Up to 2 weeks.
|
Concentric mean velocity in meters per second.
|
Up to 2 weeks.
|
|
Concentric mean power of squat
Time Frame: Up to 2 weeks.
|
concentric mean velocity in watts.
|
Up to 2 weeks.
|
|
Concentric peak power of squat
Time Frame: Up to 2 weeks.
|
Concentric peak power in watts.
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Up to 2 weeks.
|
|
Concentric rep duration of squat
Time Frame: Up to 2 weeks.
|
Concentric rep duration in scend.
|
Up to 2 weeks.
|
|
Dip of squat
Time Frame: Up to 2 weeks.
|
Dip in meters.
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Up to 2 weeks.
|
|
Eccentric min velocity of squat
Time Frame: Up to 2 weeks.
|
Eccentric min velocity in meters per second.
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Up to 2 weeks.
|
|
Eccentric peak velocity of squat
Time Frame: Up to 2 weeks.
|
Eccentric peak velocity in meters per second.
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Up to 2 weeks.
|
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Eccentric peak force of squat
Time Frame: Up to 2 weeks.
|
Eccentric peak force in newtons.
|
Up to 2 weeks.
|
|
Vertical distance of squat
Time Frame: Up to 2 weeks.
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Vertical distance in meters.
|
Up to 2 weeks.
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Tzai-Li Li, Phd, National Taiwan Sport University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- NationalTaiwanSportU
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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