Effectiveness of a Warm-Up With Foam Roller in Professional Basketball Players

July 24, 2023 updated by: Javier Reina Abellan, Universidad de Murcia

Effectiveness of a Warm-Up With Foam Roller for 3 Months in Professional Basketball Players: A Randomized Controlled Trial

The purpose of this study is to analyze the effectiveness of a foam roller warm-up on sports performance in professional basketball players.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

Twenty-two professional basketball players, divided into two randomized groups, carried out a specific warm-up for three months with a foam roller. Three measurements were made, pre-intervention, post-intervention at 12 weeks and a four-week follow-up. In these measurements reference data were taken for jumping, ankle dorsiflexion and balance. During this protocol, they performed three series of sixty seconds of application with thirty seconds of rest between series, three days a week and applied to the calf muscles, hamstrings, quadriceps, gluteus and TFL.

Study Type

Interventional

Enrollment (Actual)

22

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

    • Murica
      • Murcia, Murica, Spain, 30107
        • Universidad Católica San Antonio de Murcia

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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Masculine or feminine
  • Minimum 18 years and maximum 30
  • Professional players
  • Practice 3 training sessions per week + competition on weekends

Exclusion Criteria:

  • Musculoskeletal injury in the last 3 months
  • Surgery in the lower extremity in the last year
  • Present a diagnosed orthopedic or neurological pathology of the lower limb.

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

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Warm-up + Foam Roller
General Warm-up + Warm-up with Foam Roller
General Warm-up + Foam Roller
No Intervention: Warm-up Only
General Warm-up only

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Know the effectiveness of a warm-up with a foam roller in proffesional basketball player during 18 weeks on jumping using the Counter Movement Jump, dorsiflexión using the Lung Test and the balance using the Y-Balance Test
Time Frame: Baseline and week 18
The countermovement jump will obtain the jump height in centimetres, the ankle dorsiflexion in degrees using the Lung test and the distance in centimeters using the Y-Balance test. High scores in any of the tests will lead to a decrease in the risk of injury and an improvement in performance. A first pre-intervention measurement is carried out, another at 14 weeks post-intervention and others at 18 weeks follow-up. This is the general measure.
Baseline and week 18

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Evaluate the improvement obtained in the experimental group after a warm-up protocol with foam roller for 14weeks 3 days per week on the Counter Movement Jump, Lung Test and Y-Balance test vs non-intervention group.
Time Frame: Baseline and week 14
Observe the differences obtained after 14 weeks between the pre-intervention vs post-intervention measurement in the experimental group and in the control group. This is the specific measure.
Baseline and week 14
Maintenance of foam roller warm-up adaptations on the Counter Movement Jump, Lung Test and Y-Balance Test after intervention for a 1 month
Time Frame: Week 14 and week 18
To observe if the differences obtained after 14 weeks of intervention are maintained or not during the following 4 weeks of follow-up, between the post-intervention vs. post-follow-up measurement in the experimental group and in the control group. This is a specific measure
Week 14 and week 18

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Daniel Casado, Universidad Católica San Antonio de Murcia

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)

September 20, 2022

Primary Completion (Actual)

February 2, 2023

Study Completion (Actual)

March 15, 2023

Study Registration Dates

First Submitted

June 27, 2023

First Submitted That Met QC Criteria

July 24, 2023

First Posted (Actual)

August 2, 2023

Study Record Updates

Last Update Posted (Actual)

August 2, 2023

Last Update Submitted That Met QC Criteria

July 24, 2023

Last Verified

July 1, 2023

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Universidad Católica de Murcia

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

No research data from the participants is currently shared, the results will be published by the researchers of this study in academic journals. In the future, it is not ruled out making our data and results available to interested researchers and possible collaborators who contact specifically the researchers of our 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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