Suction Cups and Foam Roller in the Improvement of the Flexibility in Basketball Players

January 23, 2020 updated by: Investigación en Hemofilia y Fisioterapia

Efficacy of an Intervention Using the Suction Cups and the Foam Roller in the Improvement of the Flexibility of the Ischiotibial Musculature in Basketball Players From 18 to 25 Years Old. A Randomized Clinical Study

Introduction. Basketball is a predominantly anaerobic exercise that exposes to high intensity actions (jumps, speed control, accelerations and decelerations, and changes of direction). A lack of flexibility can affect the appearance of muscle injuries. Foam roller is a myofascial self-release technique using a foam roller. The suction cups are an instrumental technique where the negative pressure produces an increase in the blood flow of the tissues.

Goals. To evaluate the effectiveness of a physiotherapy intervention through suction cups and foam roller in amateur basketball players.

Study design. Randomized, single-blind clinical study with a follow-up period. Methodology. The 20 basketball players that are expected to be recruited will be randomly assigned to the two study groups: experimental (suction cups and Foam roller) and control (Foam roller). The intervention will last 4 weeks, with 2 weekly sessions. The study variable will be: hamstring flexibility (measured with finger-ground, Well and Shober tests). The analysis of normality will be carried out with the Shapiro-Wilk test. In case of homogeneity of the groups, we will use parametric tests: t-student test of repeated measures (difference between evaluations) and ANOVA of repeated means (intra and intersubject effect).

Expected results. An intervention using suction cups and foam roller is effective in improving the flexibility of the hamstring muscles in basketball players.

Study Overview

Status

Completed

Conditions

Study Type

Interventional

Enrollment (Actual)

20

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

    • Comunity Of Madrid
      • Madrid, Comunity Of Madrid, Spain, 28670
        • Universidad Europea de Madrid

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

18 years to 25 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • Age between 18 to 25 years
  • Amateur basketball players
  • Belong to the Celeste club
  • Not having any injury to the hamstring musculature at the time of the study

Exclusion Criteria:

  • At the time of the study they are included in a program of individualized strength training in lower limbs
  • Subjects with alterations in venous return or congenital coagulopathies
  • Subjects who present hypermobility
  • Not signed the informed consent document

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

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Suction cups
The technique will be performed with the subject sitting on the floor, placing the Foam roller on the back of the thigh, requesting the athlete to perform cranial and caudal movements during the established time.The intervention through the suction cups will consist of its application and produce increased flexibility of the hamstring musculature. The technique will be performed with the subject in prone position, on the stretcher, while the physiotherapist will be placed next to the member to be treated. The suckers are placed in the proximal part where the posterior musculature of the leg originates and in the distal part of the biceps femoris, semitendinosus and semimembranous insertion. This administration of the suckers will be applied during a period of 7 minutes in each member.
The technique will be performed with the subject sitting on the floor, placing the Foam roller on the back of the thigh, requesting the athlete to perform cranial and caudal movements during the established time. The stretching exercise with the Foam roller will be done during 2 minutes in each member. The intervention through the suction cups will be performed with the subject in prone position, on the stretcher. The suckers are placed in the proximal part where the posterior musculature of the leg originates and in the distal part of the biceps femoris, semitendinosus and semimembranous insertion. This administration of the suckers will be applied during a period of 7 minutes in each member.
Other Names:
  • Hamstring flexibility
Active Comparator: Foam roller
The intervention will be carried out before starting the training session. The technique will be performed with the subject sitting on the floor, placing the Foam roller on the back of the thigh, requesting the athlete to perform cranial and caudal movements during the established time. The stretching exercise with the Foam roller will be done during 2 minutes in each member.
Each session will last 18 minutes, taking place two days a week, in a period of 4 weeks. The intervention will be carried out before starting the training session. The intervention through the self-administration of Foam roller has the objective of increasing the flexibility of the isquitibial musculature. The technique will be performed with the subject sitting on the floor, placing the Foam roller on the back of the thigh, requesting the athlete to perform cranial and caudal movements during the established time. The stretching exercise with the Foam roller will be done during 2 minutes in each member.
Other Names:
  • Hamstring flexibility

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline elongation capacity of the hamstring musculature after treatment and at month
Time Frame: Screening visit, within the first seven days after treatment and after one month follow-up visit
The assessment of the elongation capacity of the hamstring musculature will be carried out by applying the Wells drawer or test. The subject will sit on the floor in front of the drawer, with the feet together and the plants resting on the front of the drawer, and the knees extended. Next, the athlete must tilt the trunk forward and extend the arms, sliding with outstretched hands until reaching the maximum stretch that allows its trunk flexion. The result that will be recorded corresponds to the point you can touch with your fingers. The unit of measurement for this test is the centimeter (the longer the length, the greater the hamstring elongation capacity).
Screening visit, within the first seven days after treatment and after one month follow-up visit

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline ischithiobial extensibility after treatment and at month
Time Frame: Screening visit, within the first seven days after treatment and after one month follow-up visit
The assessment of the ischithiobial extensibility will be made by applying the finger-floor test. The subject will have to reach the greatest possible distance from the standing position with the knees in extension, by bringing the hands (by flexing the spine) towards the ground. The evaluator will measure the distance between the tip of the third finger and the floor, with the unit of measure being the centimeter (a longer length will indicate greater hamstring extensibility).
Screening visit, within the first seven days after treatment and after one month follow-up visit
Change from baseline flexibility after treatment and at month
Time Frame: Screening visit, within the first seven days after treatment and after one month follow-up visit
The assessment of flexibility will be measured using the Schober test. The physiotherapist will stand behind the athlete, while the subject is standing with legs extended. The evaluator will mark a line that will connect both posterior superior iliac spines, at the level of the spinous process of the fifth lumbar vertebra. Later a second mark will be made 10 centimeters away in the cranial direction to the first. Next, the subject will be asked to perform maximum flexion of the spine keeping the knees extended. When the subject is in that position of maximum column flexion, a measurement of the distance between the two marks will be made, comparing this result with the initial distance of 10 centimeters. The centimeter is the unit of measurement and a higher score indicates greater muscle flexibility.
Screening visit, within the first seven days after treatment and after one month follow-up visit

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 10, 2019

Primary Completion (Actual)

April 20, 2019

Study Completion (Actual)

June 20, 2019

Study Registration Dates

First Submitted

March 4, 2019

First Submitted That Met QC Criteria

March 4, 2019

First Posted (Actual)

March 6, 2019

Study Record Updates

Last Update Posted (Actual)

January 27, 2020

Last Update Submitted That Met QC Criteria

January 23, 2020

Last Verified

January 1, 2020

More Information

Terms related to this study

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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