Effects of 6-Week Vibration and Non-Vibration Foam Rolling
Comparison of the Effects of 6-Week Vibration and Non-Vibration Foam Rolling on Neuromuscular Control and Performance in Male Soccer Players
1 other identifier
interventional
36
1 country
1
Brief Summary
This study aims to compare the effects of 6-week vibration and non-vibration foam rolling on neuromuscular control and performance in male soccer players.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable healthy-volunteers
Started Aug 2023
Shorter than P25 for not_applicable healthy-volunteers
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 4, 2023
CompletedStudy Start
First participant enrolled
August 7, 2023
CompletedFirst Posted
Study publicly available on registry
August 14, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 25, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
October 2, 2023
CompletedNovember 2, 2023
October 1, 2023
2 months
August 4, 2023
October 31, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Knee Flexor and Extensor Muscle Strength
Participants' knee flexor and extensor muscle strength will be evaluated with the Lafayette manual muscle test device (Lafayette Instrument Company, Lafayette IN, USA).This device is a valid and reliable method that is frequently used in the evaluation of muscle strength. During the evaluation, participants will be asked to perform a maximum isometric contraction for 3 seconds with the muscle in which the muscle strength is evaluated against the resistance to be applied with the manual muscle test device. Measurements will be repeated 3 times with one minute intervals for the right and left sides and the average of the measured values will be used for analysis.
A week
Knee Flexor and Extensor Muscle Strength Ratio (H/Q Ratio)
Participants' Hamstring/Quadriceps muscle strength ratio will be evaluated with the Lafayette manual muscle test device (Lafayette Instrument Company, Lafayette IN, USA). This device is a valid and reliable method that is frequently used in the evaluation of muscle strength. The Hamstring/Quadriceps muscle strength ratio will be determined by the ratio of the knee flexor and extensor muscle strengths obtained during the measurements.
A week
Flexibility
The flexibility will be evaluated whit the sit-and-reach test. The testing box will be fixed to the wall, and participants will be requested to sit with their knees extended and the soles of their feet against the testing box. Then participants will be requested to slowly reach forward as far as possible along the top of the box and hold the position for 2 seconds without bending their knees. The average of the two trials will be used for analysis.
A week
Secondary Outcomes (5)
Dynamic Balance
A week
Agility
A week
Sprint
A week
Reaction Time
A week
Anaerobic Power
A week
Study Arms (3)
Vibration Foam Rolling Group
ACTIVE COMPARATORThe vibration foam rolling method will be applied to the gluteal, tensor fascia latae, hamstring, quadriceps femoris, and gastrocnemius muscles of both lower extremities of the participants in the Vibration Foam Rolling Group, in addition to the routine warm-up protocol, 3 days a week for a total of 15 minutes a day for 6 weeks.
Non-Vibration Foam Rolling Group
ACTIVE COMPARATORThe non-vibration foam rolling method will be applied to the gluteal, tensor fascia latae, hamstring, quadriceps femoris, and gastrocnemius muscles of both lower extremities of the participants in the Non-Vibration Foam Rolling Group, in addition to the routine warm-up protocol, 3 days a week for a total of 15 minutes a day for 6 weeks.
Control Group
NO INTERVENTIONNo intervention will be applied to the control group. This group will continue the routine warm-up protocol.
Interventions
The vibration foam rolling method will be applied to the gluteal, tensor fascia latae, hamstring, quadriceps femoris, and gastrocnemius muscles of both lower extremities of the participants in the Vibration Foam Rolling Group, in addition to the routine warm-up protocol, 3 days a week for a total of 15 minutes a day for 6 weeks.
The non-vibration foam rolling method will be applied to the gluteal, tensor fascia latae, hamstring, quadriceps femoris, and gastrocnemius muscles of both lower extremities of the participants in the Non-Vibration Foam Rolling Group, in addition to the routine warm-up protocol, 3 days a week for a total of 15 minutes a day for 6 weeks.
Eligibility Criteria
You may qualify if:
- Volunteering to participate in the study.
- To regularly participate in team training within the club.
- To have been playing football for at least 1 year in the category.
You may not qualify if:
- Having any sports injury involving the lower extremity and/or spine in the last 3 months.
- Having a problem (vertigo, neuropathy, etc.) that may negatively affect balance and coordination.
- Having a musculoskeletal deformity (short limb, etc.) concerning the lower and upper extremities.
- Implementing a training program outside of routine team training
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Celal Bayar Universitylead
- Izmir Katip Celebi Universitycollaborator
Study Sites (1)
İzmir Katip Celebi University
Izmir, Turkey (Türkiye)
Related Publications (1)
Secer E, Kaya DO. Effects of 6-Week Vibration vs. Nonvibration Foam Rolling on Performance-Related Physical Fitness Parameters in Young Male Soccer Players: A Randomized Controlled Trial. J Strength Cond Res. 2025 May 1;39(5):e647-e658. doi: 10.1519/JSC.0000000000005062. Epub 2025 Mar 4.
PMID: 40030119DERIVED
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Masking Details
- The control group will receive a routine warm-up protocol. Outcome measurement will be performed by an investigator who was blinded to group allocation
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 4, 2023
First Posted
August 14, 2023
Study Start
August 7, 2023
Primary Completion
September 25, 2023
Study Completion
October 2, 2023
Last Updated
November 2, 2023
Record last verified: 2023-10