- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07113249
- Original Trial
The Effects of Foam Rolling on Ankle Dorsiflexion, Ankle Stability, and Athletic Performance in Rhythmic Gymnasts
August 12, 2025 updated by: Giacomo Belmonte, University of Palermo
The Effects of Foam Rolling During the Warm-Up Phase on Range of Motion, Ankle Stability and Leaping Performance in Young Elite Rhythmic Gymnasts
Rhythmic Gymnastics is an Olympic discipline featuring individual or team competition.
Regardless of the type of competition, athletes undergo rigorous training focused on enhancing their coordination, joint range of motion, and jump height.
Each rhythmic gymnast voluntarily underwent testing at their own gym after reading and signing the informed consent document.
During the first session, general information was collected on all participants (age, weight, and height), followed by an assessment of athletic performance and joint mobility parameters.
For the jump performance parameters, the Counter Movement Jump test (CMJ) was used through an optical detecting system.
An inertial sensor was used to measure joint mobility, while a pressure platform was used to measure ankle stability, using a single-leg jump protocol.
Subsequently, participants were randomly divided into two groups: an experimental group (EG) and a control group (CG).
The EG performed three sets, each lasting 60 seconds, with a 30-second break between sets for two times for week for 3 weeks.
During each FR session, a complete sequential movement was always performed, starting from the gastrocnemius muscles and ending with the soleus muscle.
At the end of the three weeks, all measurements were repeated.
Study Overview
Study Type
Interventional
Enrollment (Actual)
26
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
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-
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Palermo, Italy, 90144
- University of Palermo
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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
- Child
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Active participation in competitive training programs (at least 10 hours per week), at least one year of experience in competitions organized by the Italian Gymnastics Federation, and no recent injuries.
Exclusion Criteria:
- Presence of current or not fully recovered injuries to the ankle or foot, and irregular participation in training sessions within the four weeks preceding the study.
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: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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No Intervention: Control Group (CG)
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Experimental: Experimental: Foam Rolling (FR)
Three sets, each lasting 60 seconds, with a 30-second break between sets for two times for week.
During each FR session, a complete sequential movement was always performed, starting from the gastrocnemius muscles and ending with the soleus.
A metronome was set to play one complete repetition every 2 seconds to establish the speed of execution.
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For the FR, participants were asked to place the roller behind their leg.
Three sets, each lasting 60 seconds, with a 30-second break between sets, were performed, for a total of 90 rolls per set.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Counter Movement Jump (CMJ)
Time Frame: At the beginning of enrollment ( Baseline, T0) and the end of the 3-week treatment (T1)
|
Initially, the athlete stands upright on a flat surface or force platform, feet shoulder-width apart, hands on hips (to eliminate arm swing).
Without a pause, the athlete performs a quick downward movement (countermovement) by bending the knees and hips, then immediately jumps vertically as high as possible.
The athlete lands in an upright position on the same spot, trying to absorb the impact with knees slightly bent.
Jump height and flight time is recorded using an optical system, Optojump™ system(Microgate, Bolzano, Italy) connected to a personal computer with dedicated software(OptojumpTM Next software).
The system consists of two optical bars, a receiver and a transmitter, positioned 1m apart.
The bars identify ground contact time(with a precision of 1ms) and then convert non-contact time into cm.
Based on recommendations on optimal jump height (20 to 60cm).
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At the beginning of enrollment ( Baseline, T0) and the end of the 3-week treatment (T1)
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Ankle Dorsiflexion ROM
Time Frame: At the beginning of enrollment ( Baseline, T0) and the end of the 3-week treatment (T1)
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Each participant was fitted with an inertial sensor (Beyond Inertial, Motusech, Roma, Itay) in the center of the foot, using an elastic band supplied with the sensor.
The starting position was standardized with the subjects sitting on a medical bed with the popliteal cord attached to the edge of the bed, forming a 90° angle.
The position of the foot, on the other hand, was placed in a neutral position using a laser level.
Subsequently, the dorsal flexion movement was performed.
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At the beginning of enrollment ( Baseline, T0) and the end of the 3-week treatment (T1)
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Ankle Stability
Time Frame: At the beginning of enrollment ( Baseline, T0) and the end of the 3-week treatment (T1)
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Ankle stability was assessed using a functional monopodalic protocol, which involved four jumps on one foot: two per leg, both frontally and laterally.
These jumps were performed by stepping over an adjustable obstacle set at 70% of the maximum height reached on a pressure platform (SensorMedica freeMed 40×40, Guidonia Montecelio, Italy).
The platform has an active sensory surface of 40×40 cm with a thickness of only 8 mm and a low weight of approximately 4 kg.
Inside, there are resistive sensors coated in 24K gold on conductive rubber, with a density of approximately 10,000 sensors/m².The acquisition frequency is high, up to 400 Hz, allowing for detailed dynamic analysis, and the sensors have a life cycle of over 1,000,000 cycles of use
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At the beginning of enrollment ( Baseline, T0) and the end of the 3-week treatment (T1)
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
May 1, 2025
Primary Completion (Actual)
June 15, 2025
Study Completion (Actual)
June 30, 2025
Study Registration Dates
First Submitted
August 2, 2025
First Submitted That Met QC Criteria
August 2, 2025
First Posted (Actual)
August 8, 2025
Study Record Updates
Last Update Posted (Actual)
August 17, 2025
Last Update Submitted That Met QC Criteria
August 12, 2025
Last Verified
July 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- 62141-2025-1
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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