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Completed

NCT Number: NCT06423157

Plyometric and Stability Exercise Protocol in Female Basketball Players

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.

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Key information

Age range

18 year–30 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Universidad Católica San Antonio, Murcia

Murcia, 30107, Spain

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Intervention

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.

Primary outcomes

  1. Assess the changes in vertical jump

    Time frame: Screening visit, within the first seven days after treatment and after six weeks follow-up

    The vertical jump will be measured with the My jump 2.0® application. The athlete will be asked to jump as high as possible from a standing position, raising the body in the air by means of an impulse generated by the leg muscles. The evaluation consists of the recording of the jump, the calculation of the height of the vertical jump and the athlete's strength and speed levels. The unit of measurement of this tool is the centimetre, where the greater the distance, the higher the vertical jump.

Secondary outcomes

  1. Assess the changes in stability

    Time frame: Screening visit, within the first seven days after treatment and after six weeks follow-up

    Stability is measured using the Y balance test. Three strips of adhesive tape are placed on the floor in a Y shape. The athlete, placed in the centre of the Y, will maintain unipodal balance while with the contralateral leg trying to reach the farthest point in each direction (anterior, posteromedial and posterolateral), without lifting the heel of the supporting foot which is the one being evaluated. Three attempts shall be made with each leg. The distance is measured with a tape measure, in centimetres (19), where the greater the distance, the greater the stability.

  2. Assess the changes in flexibility

    Time frame: Screening visit, within the first seven days after treatment and after six weeks follow-up

    Flexibility will be assessed with the Sit and Reach test. The athlete will sit on the floor, with her knees straight and her feet placed against the edge of a box. From this position, the participant shall progressively perform a trunk flexion, trying to reach as far as possible with the tips of her hands on the scale graduated in centimetres on the box. The unit of measurement for this test is the centimetre, where the greater the distance reached, the greater the flexibility.

  3. Assess the changes in agility

    Time frame: Screening visit, within the first seven days after treatment and after six weeks follow-up

    Agility will be assessed with the T-Test. Four cones should be placed in a T-shape: A at the starting point; B at 9.14 m forward; and C and D at the sides of this at 4.57 m the other two cones. The athlete must go as fast as possible to cone B and touch it with the tip with her right hand, then she must go to the sides touching cones C and D with the hand of the same side, return to touch cone B with the left hand and lastly, move backwards and go over cone A. The unit of measurement is the second, where lower times indicate efficient agility.

Sponsors and collaborators

Lead sponsor

Universidad Católica San Antonio de Murcia

Other

Registry information

Official study title

Efficacy of a Plyometric and Stability Exercise Protocol in Female Basketball Players. A Controlled Clinical Study.

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
May 21, 2024
Registry last updated
Mar 25, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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