Effect of Weekly Plyometric Training Frequency on Youth Female Basketball Players: A Comparison of Two vs. Four Sessions

April 2, 2024 updated by: Bruno Figueira
Players were randomly assigned to a two-times-a-week (2PLYO, n = 15) or four-times-a-week (4PLYO, n = 15) PT (Plyometric Training) group. Both groups performed the same weekly total volume of jumps during PT in addition to regular basketball training and competition. The 2PLYO group performed 240 jumps over two sessions (120 jumps per session), and the 4PLYO group performed 240 jumps over four sessions (60 jumps per session). After the eight-week intervention, all players underwent a one-week detraining period with no PT training while basketball training and competitions continued. Testing was performed at baseline (pre-test), after intervention (post-test), and after the detraining period. Players were assessed for lower body power using jump tests (countermovement jump [CMJ], drop-jump [DJ] from a 20-cm box, and horizontal jump [HJ]; change of direction ability using a planned agility test; and speed using a 20-m sprint and a 5-m split.

Study Overview

Status

Completed

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

30

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

      • Kaunas, Lithuania
        • Vytutas Magnus University

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

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Minimum of four basketball training sessions with at least 90-min duration and one competitive game per week.

Exclusion Criteria:

  • Musculoskeletal, neurological, or orthopedic injury that may impair their participation.

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: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: 2PLYO
The 2PLYO (two-times-a-week) group performed 240 jumps over two sessions (120 jumps per session).
Players were randomly assigned to a two-times-a-week (2PLYO, n = 15) or four-times-a-week (4PLYO, n = 15) PT group. Both groups performed the same weekly total volume of jumps during PT in addition to regular basketball training and competition. After the eight-week intervention, all players underwent a one-week detraining period with no PT training while basketball training and competitions continued. Testing was performed at baseline (pre-test), after intervention (post-test), and after the detraining period. Players were assessed for lower body power using jump tests (countermovement jump [CMJ], drop-jump [DJ] from a 20-cm box, and horizontal jump [HJ]; change of direction ability using a planned agility test; and speed using a 20-m sprint and a 5-m split.
Experimental: 4PLYO
The 4PLYO (four-times-a-week) group performed 240 jumps over four sessions (60 jumps per session)
Players were randomly assigned to a two-times-a-week (2PLYO, n = 15) or four-times-a-week (4PLYO, n = 15) PT group. Both groups performed the same weekly total volume of jumps during PT in addition to regular basketball training and competition. After the eight-week intervention, all players underwent a one-week detraining period with no PT training while basketball training and competitions continued. Testing was performed at baseline (pre-test), after intervention (post-test), and after the detraining period. Players were assessed for lower body power using jump tests (countermovement jump [CMJ], drop-jump [DJ] from a 20-cm box, and horizontal jump [HJ]; change of direction ability using a planned agility test; and speed using a 20-m sprint and a 5-m split.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Horizontal jump
Time Frame: 10 weeks

Players performed two jumps for each protocol, with one minute of rest provided between trials and three minutes of rest between protocols. The best result was recorded for analysis.

In the HJ, a metric tape was used to measure the length between the players' starting position and the nearest point of landing contact (i.e., the back of the heels). The players begin standing with their toes positioned against a marker. Players initiated the jump with countermovement and arm swing, jumping horizontally as far as possible and landing on both feet. The jump was invalid if the players did not land properly on their feet or fell back.

10 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
CMJ
Time Frame: 10 weeks
Players performed two jumps [19] for each protocol, with one minute of rest provided between trials and three minutes of rest between protocols. The best result was recorded for analysis. CMJ height was calculated with an Optojump system (Microgate, Bolzano, Italy). For the CMJ, participants began by standing upright. Upon readiness, the athlete squatted down until the knees were bent at a 90-degree angle and then immediately executed a vertical jump as high as possible. Throughout the test, participants kept their hands on their hips[20].
10 weeks

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Drop Jump
Time Frame: 10 weeks

Players performed two jumps [19] for each protocol, with one minute of rest provided between trials and three minutes of rest between protocols. The best result was recorded for analysis. DJ height were calculated with an Optojump system (Microgate, Bolzano, Italy).

The optimal DJ height was determined in the initial familiarization session. Following preliminary pilot testing, each player performed three DJs from two heights (90 and 110 cm) with 1-min intervals. The highest jump height/contact time ratio was considered the optimal height. In the DJ, the players drop from the optimal with one foot, landing with 2 feet simultaneously, and then immediately perform a maximal jump [21]. The RSI was calculated by dividing flight time (ms) by contact time (ms) [22].

10 weeks
Drop jump (RSI)
Time Frame: 10 weeks
The RSI was calculated by dividing flight time (ms) by contact time (ms) [22].
10 weeks
Linear sprint-5m
Time Frame: 10 weeks
Participants performed two 20-m sprints (with 5-m split time also recorded), with at least three minutes of rest between them. The fastest performance trial was used for data analysis. During the recovery period between sprints, the participants returned to the starting line and waited for the second trial. Sprint times were recorded with electronic photocells (Timing-Radio Controlled; TTSport, San Marino, CA, USA) placed 5-m- and 20-m from the starting line. Players were instructed to start the sprints from a line set 0.3-m behind the start line and to run as quickly as possible through the final pair of sensors [19]. During each trial, players were also verbally encouraged to produce their maximal effort.
10 weeks
Linear sprint-20m
Time Frame: 10 weeks
Participants performed two 20-m sprints (with 5-m split time also recorded), with at least three minutes of rest between them. The fastest performance trial was used for data analysis. During the recovery period between sprints, the participants returned to the starting line and waited for the second trial. Sprint times were recorded with electronic photocells (Timing-Radio Controlled; TTSport, San Marino, CA, USA) placed 5-m- and 20-m from the starting line. Players were instructed to start the sprints from a line set 0.3-m behind the start line and to run as quickly as possible through the final pair of sensors [19]. During each trial, players were also verbally encouraged to produce their maximal effort.
10 weeks
Change of direction
Time Frame: 10 weeks
The players performed the CODS [23] test to measure the change of direction ability. The players performed two trials separated by three minutes of rest. The fastest of the two trials was used for analysis. Single-beam measure were taken using electronic photocells (Timing-Radio Controlled; TTSport, San Marino, CA, USA) which is previously validated system [24], positioned 3 meters apart and located on either side of the start and finish lines. All photocells were mounted at a height of 1 m above the floor, the maximum height of the manufacturer's standard tripods. The players started the trials from a line placed 0.3-m behind the start line. During each trial, players were strongly verbally encouraged to produce their maximal effort.
10 weeks

Collaborators and Investigators

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

November 1, 2023

Primary Completion (Actual)

January 20, 2024

Study Completion (Actual)

February 20, 2024

Study Registration Dates

First Submitted

March 21, 2024

First Submitted That Met QC Criteria

April 2, 2024

First Posted (Actual)

April 9, 2024

Study Record Updates

Last Update Posted (Actual)

April 9, 2024

Last Update Submitted That Met QC Criteria

April 2, 2024

Last Verified

April 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • 2vs4

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP

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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