Plyometric and Stability Exercise Protocol in Female Basketball Players

NCT ID: NCT06423157

Last Updated: 2025-03-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

19 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-05-19

Study Completion Date

2024-07-01

Brief Summary

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Introduction. Basketball is a high intensity intermittent sport, requiring jumping, running, accelerations and decelerations with changes of direction and lateral movements. Plyometric exercises are a training technique that consists of a cycle of muscle stretching and shortening in which the energy stored in the eccentric phase (lengthening) is released facilitating the production of maximum power in the concentric phase (shortening).

Objective. To analyse the efficacy of a physiotherapy intervention through a protocol of plyometric and stability exercises in the improvement of vertical jump, stability, flexibility and agility in federated female basketball players. The primary variable will be the vertical jump (My jump 2.0). Secondary variables will be stability (Y balance test), flexibility (Sit and Reach) and agility (T-Test).

Methods. Controlled, single-blind clinical study. 20 athletes will be randomised to the experimental and control groups. The intervention of the experimental group will consist of a protocol using plyometric and stability exercises. The athletes included in the control group will not perform any intervention and will continue with their usual routine. The intervention period will last 6 weeks, with a periodicity of 2 weekly sessions of 20 minutes each.

Detailed Description

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Conditions

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Sports Physical Therapy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Outcome Assessors
Three assessments will be made throughout the study: before the intervention (T0), after the experimental phase (T1) and after a 6-week follow-up period (T2). All variables will be assessed by an evaluator blinded to the assignment of the athletes to the study groups.

Study Groups

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Experimental group

The intervention period will last 6 weeks, with a periodicity of 2 weekly sessions of 20 minutes each. All interventions will take place at the Palacio de los Deportes de Murcia. All interventions will be carried out by the same physiotherapist, following the same protocol.

The intervention of the experimental group will consist of a protocol using plyometric and stability exercises.

Group Type EXPERIMENTAL

Intervention

Intervention Type OTHER

The intervention period will last 6 weeks, with a periodicity of 2 weekly sessions of 20 minutes each. All interventions will take place at the Palacio de los Deportes de Murcia. All interventions will be carried out by the same physiotherapist, following the same protocol. The intervention of the experimental group will consist of a protocol using plyometric and stability exercises.

Control group

The athletes included in the control group will not undergo any intervention and will continue with their usual routine.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Intervention

The intervention period will last 6 weeks, with a periodicity of 2 weekly sessions of 20 minutes each. All interventions will take place at the Palacio de los Deportes de Murcia. All interventions will be carried out by the same physiotherapist, following the same protocol. The intervention of the experimental group will consist of a protocol using plyometric and stability exercises.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Female players over 18 years of age.
* That during the study period they play basketball competing in the 1st Women's Division 1 category of the Basketball Federation of the Region of Murcia.
* That they perform strength exercises at least once a week.
* That they sign the informed consent document.

Exclusion Criteria

* Players with knee or ankle injuries in the 6 months prior to the study.
* Players who use ankle or knee braces regularly.
* Players with lower limb surgery in the last year.
* Players whose participation is contraindicated by the team doctor, physiotherapist or physical trainer.
Minimum Eligible Age

18 Years

Maximum Eligible Age

30 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Universidad Católica San Antonio de Murcia

OTHER

Sponsor Role lead

Responsible Party

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Rubén Cuesta-Barriuso, PhD

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Universidad Católica San Antonio, Murcia

Murcia, , Spain

Site Status

Countries

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Spain

Other Identifiers

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PlyoBask

Identifier Type: -

Identifier Source: org_study_id

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