CClinicalTrials.gg
CompletedNCT03870321Updated Jan 27, 2020

Core Training to Improve Abdominal Strength Strength and Ankle Proprioception in Basketball Players

An interventional study of Core training in Proprioceptive Disorders, sponsored by Investigación en Hemofilia y Fisioterapia. Completed at 1 site in Spain. Open to male participants aged 18 Years to 40 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2020-01-27.

Sponsored by Investigación en Hemofilia y Fisioterapia · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
18 Years to 40 Years
Sex
Male
01

Study summary

Introduction. The prevalence of ankle injuries in basketball are high. The lack of balance in the ankle is one of the main causes that produces these injuries. The goal of core training is to increase the physical capacities of resistance strength in the abdomen and analyze if it produces improvement in proprioception in the ankle joint in basketball players.

Objective. To evaluate the effectiveness of Core training to improve the strength of the abdomen and analyze if it produces improvement in proprioception in ankle of basketball players.

Study design. Randomized, multicentric, single-blind clinical study with a follow-up period.

Methods. The 30 participants recruited will be randomly assigned to the two study groups: experimental (Core training for strength in the abdomen) and control (without intervention). The treatment will last 4 weeks, with 3 weekly sessions, approximately 20 minutes each. There will be three evaluations (pre-intervention, post-intervention and follow-up). On the dependent variables: strength core resistance (evaluated with Trunk Flexor Test, Trunk Extender Test, and Side Bridge Test) and proprioception (measured with the Star Excursion Balance tests and Romberg test) With the Kolmogorov Smirnov statistical test we will calculate the normality and with the t-student test of paired data and an ANOVA of repeated measures, we will obtain the difference between the three evaluations and the intra and intersubject effect, respectively.

Expected results. To observe improvement in strength in the abdomen and analyze if it produces improvement in proprioception in the ankle of basketball players.

02

Conditions studied

  • Proprioceptive Disorders

Keywords

  • Core
  • Strength
  • Proprioception
  • Ankle
  • Basketball
03

In context

Somatosensory Disorders

61 studies on the registry are indexed under Somatosensory Disorders; 8 are open to participants now.

This study's enrollment of 30 is below the median of 40 across 42 interventional studies indexed under Somatosensory Disorders.

Browse Somatosensory Disorders studies →

Lead sponsor

Investigación en Hemofilia y Fisioterapia is the lead sponsor of 54 studies on the registry; 6 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes

Inclusion criteria

  • Basketball players
  • Federated in the Community of Madrid
  • Male
  • With an age range of 18 to 40 years.

Exclusion criteria

Exclusion Criteria:

  • Who have a musculoskeletal injury at the time of the study or who have suffered a lower limb injury in a period of three months before the study
  • That they are in an individualized personal training
  • Not signed the informed consent document.
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
30 participants (actual)

Study arms

  • Experimental
    Core training

    The subjects who are in the experimental group will carry out the Core training routine

    Other: Core training

  • No intervention
    Control

    The subjects who are in the control group will not receive intervention and will continue with their daily routine and training

Interventions

  • OtherCore training

    In the first week different types of abdominal exercises will be performed: standard, with trunk rotation, extension of the back raising the upper extremity of the body and legs, extension of the back raising one arm and the contralateral leg. In the same way, the subject will raise from the quadruped position one arm and the contralateral leg on each side, and we will ask for the exercise of the front plate, positioning itself in a position of four support points: feet and elbows. When performing the rear bridge exercise the subject will raise the trunk resting on both feet, while in the lateral bridge exercise will be done with support on the right and left side. All exercises will be done for 30 seconds, in 3 series). During the next three weeks we will continue with the same training, but for each week we will increase 10 seconds per exercise.

06

What researchers measure

Primary outcomes

  1. Change from baseline ankle proprioception after intervention and at month

    The Star excursion balance test will be used to measure ankle proprioception. It begins with a star drawn on the ground, while the subject will remain in a static position, placing his or her bare foot in the center of the star. During the execution of the test the subject will be asked to touch the farthest point possible with the tip of the first finger. The contact of the finger has to be clean, without supporting the weight or imbalance of the other foot, returning each time to the initial monopodal position. At each attempt the contact point will be recorded on the ground line. This exercise will be repeated three times and the average of the evaluations will be taken into account to obtain the value of the measurement in each one of the directions to be studied, with the final result being the average distance of all the attempts in each of the directions. The unit of measurement is the centimeter (the greater distance in centimeters, the better ankle proprioception).

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

Secondary outcomes

  1. Change from baseline strength of the flexor muscles of the abdomen after intervention and at month

    The Trunk Flexor Test will be used to measure the strength of the flexor muscles of the abdomen. The subject will be sitting on a bench, with knees and hips bent at 90 degrees and feet tied to the stretcher. The arms should be crossed over the chest and trunk in a flared position at 60 degrees. The subject must maintain that position as long as possible. The test is terminated when the participant can not sustain the initial position. The unit of measure is temporary (seconds). The greater the amount of time, the greater the strength of the flexor muscles of the abdomen.

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

  2. Change from baseline strength of the extensor muscles of the abdomen after intervention and at month

    Researchers will use the Trunk Extender Test to evaluate the strength of the extensor muscles of the abdomen. The athlete will be placed in prone position, with the pelvis and ankles fixed to the stretcher with a strap, with the navel on the edge of the stretcher. A chair should be placed at the same height as the stretcher to support the trunk and upper extremity. Then the chair will be removed and the subject should maintain a horizontal position with arms crossed to the trunk as long as possible. The test ends when the subject can not hold the initial position anymore and touch the chair in front of them with their hands. The unit of measure is temporary (seconds). The greater the amount of time, the greater the strength of the extensor muscles of the abdomen.

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

  3. Change from baseline strength of the lateral flexor muscles of the abdomen after intervention and at month

    The Side Bridge Test will be used to measure the strength of the lateral flexor muscles of the abdomen. The subject will be placed in the lateral decubitus with the knees extended on the stretcher being asked to lift the hip of the stretcher using only the feet and the elbow as support. The test will end when the hip falls. The unit of measure is temporary (seconds). The greater the amount of time, the greater the strength of the lateral flexor muscles of the abdomen.

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

  4. Change from baseline ankle proprioception after intervention and at month

    The Romberg test will be used to measure proprioception. The athlete will be asked to stand with their feet together, their arms loose on their sides and their eyes open. In this position any imbalance will be recorded and subsequently you will be asked to close your eyes. The stability will be observed and it will be compared with the one presented with the eyes open. The degree of oscillation and the direction of hips, knees and the entire body should be evaluated. The test is considered positive if there is an imbalance or if the oscillation worsens significantly with the closing of the eyes (score 1). Otherwise, it will be negative (score 0).

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

07

Study locations

1 site
  • Universidad Europea de Madrid
    Madrid, Comunity Of Madrid 28670, Spain
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 27, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT03870321
Lead sponsor
Investigación en Hemofilia y Fisioterapia
Responsible party
Sponsor
First posted
Mar 12, 2019
Start date
Apr 1, 2019
Primary completion
May 15, 2019
Completion
Jun 20, 2019
Last update
Jan 27, 2020

Study contacts

Rubén Cuesta-Barriuso, PhD
principal investigator · Universidad Europea de Madrid

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2020. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion