- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05971316
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
Conditions
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.
Sponsor
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
Keywords
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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