Functional and Performance Effects of a 4-week Weightlifting Program in Highly Trained Adolescent Basketball Athletes

November 28, 2023 updated by: Fernando Domínguez-Navarro, University of Valencia
Weightlifting is an increasingly used intervention in the sport field to improve both function and performance outcomes. However, the effects in a pediatric and adolescent population are not well described, and require further research to elucidate the benefits and potential adverse effects compared to other strength training methods, such as plyometric training.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Highly trained male and female adolescent basketball athletes aged 12-16 years will be recruited for the study. Participants will be randomly assigned to a 4-week program (12 sessions) of weightlifting or plyometric training. The training programs will be identical in sets and repetitions, progressively evolving each week towards fewer sets and fewer repetitions. The training intensity will be the same in both groups, calculated from the RM, starting at 70% in the first week and progressing by 5% each week until a final intensity of 85% in the last week. Therefore, both interventions evolve towards sessions with fewer sets and repetitions and higher loads.

The weightlifting intervention refers to the performance of highly technical and explosive multi-joint strength exercises. The program consists of six basic weightlifting maneuvers (hang power clean, overhead squat, hang power snatch, clean, split jerk, snatch), two of which are performed in each of the three weekly sessions. The order of execution of the exercises in the weekly sessions is always the same. To ensure the correct execution of the maneuvers, before starting the intervention, a brief familiarization program will be carried out. This consists of an explanation of the exercises by the research staff and practice by the participants with simultaneous correction.

The plyometric program follows the same structure, consisting in a total of 6 exercises (Max countermovement jump, double leg side jump, maximum squat jump, dropjump (20cm), single leg hurdle jump, doble leg multi hop) performed in groups of 2 for each weekly training session.

The design of the intervention program is based on previously published related articles.Training sessions will be supervised by a member of the research team with expertise in strength and conditioning in basketball athletes.

Study Type

Interventional

Enrollment (Actual)

46

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

      • Valencia, Spain, 46010
        • Fernando Domínguez Navarro

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

Yes

Description

Inclusion Criteria:

  • Healthy highly-trained basketball athletes

Exclusion Criteria:

  • Current injury or complaining limiting sports activity
  • No histoy of injury receiving non-operative treatment in the last 3 months
  • No history of injury receiving operative treatment in the last 9 months
  • Subjects who have previously carried out weightlifting training for at least 4 weeks of duration.
  • Subjects physically unable to perform a strength training program

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Weigthlifting
It consists of a 4-week strength training program based on weightlifting. Participants received previously education-training program on how to correctly perform the technique.
4-week weightlifting strength training
Active Comparator: Plyometric training
It consists of a 4-week strength training program based on plyometric exercises.
4-week weightlifting strength training

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline Repetition Maximum at 5 weeks
Time Frame: (I) Baseline: previous week before starting intervention, and (II) 5 weeks after baseline
It refeers to the maximum weight that an athlete can lift correctly in one repetition. The maximum weight lifted is recorded in kg.
(I) Baseline: previous week before starting intervention, and (II) 5 weeks after baseline
Change from baseline Hand Grip at 5 weeks
Time Frame: (I) Baseline: previous week before starting intervention, and (II) 5 weeks after baseline
Measured with validated dynamometer equipment, it register the isometric strength that an athlethe perform in a hand grip contraction. Strength is recorded in kg. Three valid measures will be recorded and the mean value will be calculated.
(I) Baseline: previous week before starting intervention, and (II) 5 weeks after baseline
Change from baseline Lower-limb muscle strength at 5 weeks
Time Frame: I) Baseline: previous week before starting intervention, and (II) 5 weeks after baseline
Force Frame system equipment will be used to assess the isometric strength for lower-limb (hip and knee) muscles. Strength values will be expressed in kg. Three valid measures will be recorded and the mean value will be calculated.
I) Baseline: previous week before starting intervention, and (II) 5 weeks after baseline

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline Ankle Mobility at 5 weeks
Time Frame: (I) Baseline: previous week before starting intervention, and (II) 5 weeks after baseline
Check-your motion (R) device (validated) will be used to evaluate ankle dorsiflexion in weigth-bearing. position.Three valid measures will be recorded and the mean value will be calculated. Results will be expressed in cm
(I) Baseline: previous week before starting intervention, and (II) 5 weeks after baseline
Change from baseline 20 meters Sprint at 5 weeks
Time Frame: (I) Baseline: previous week before starting intervention, and (II) 5 weeks after baseline
From motion cameras, the time (seconds) that an athlete takes to perform a straight line movement of 20 meters at maximum speed will be recorded.
(I) Baseline: previous week before starting intervention, and (II) 5 weeks after baseline
Change from baseline Counter movement jump (CMJ) test at 5 weeks
Time Frame: (I) Baseline: previous week before starting intervention, and (II) 5 weeks after baseline
CMJ will be used as perfomance-based outcome. Athlete, in standing position, will perform a maximum vertical jump with both hands placed on the hips. The data will be collected with the Chronojump contact platform equipment, (Boscosystem®, Barcelona, Spain), registering the flight height (cm) and power (watts). Three valid measures will be recorded and the mean value will be calculated.
(I) Baseline: previous week before starting intervention, and (II) 5 weeks after baseline
Change from baseline Hop test distance at 5 weeks
Time Frame: (I) Baseline: previous week before starting intervention, and (II) 5 weeks after baseline
This test will be used to evaluate longitudinal maximum hop performance, registering the distance reached in cm. The procedure will be performed unilaterally with both legs. A tape measure will be used to record the distance traveled. Three valid measures will be registered and the mean will be calculated
(I) Baseline: previous week before starting intervention, and (II) 5 weeks after baseline
Weight
Time Frame: Baseline
Weight will be recorded from a validated electronic scale, expressed in kg.
Baseline
Height
Time Frame: Baseline
The height of the athletes will be measured using the vertical tape measure of a manual scale.
Baseline

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)

March 6, 2023

Primary Completion (Actual)

May 30, 2023

Study Completion (Actual)

October 20, 2023

Study Registration Dates

First Submitted

February 8, 2023

First Submitted That Met QC Criteria

April 19, 2023

First Posted (Actual)

April 24, 2023

Study Record Updates

Last Update Posted (Actual)

November 29, 2023

Last Update Submitted That Met QC Criteria

November 28, 2023

Last Verified

November 1, 2023

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • UV-INV_ETICA-1523453

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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