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Effects of 6-Week Vibration and Non-Vibration Foam Rolling

C

Celal Bayar University

Status

Completed

Conditions

Healthy Volunteers

Treatments

Other: Non-Vibration Foam Rolling
Other: Vibration Foam Rolling

Study type

Interventional

Funder types

Other

Identifiers

NCT05988268
CBU-FTR-ES-O3

Details and patient eligibility

About

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.

Full description

The typical warm-up protocol consists of different stretching exercises, sub-maximal aerobic activities, and sports-related activities. However, in recent years, warm-up protocols involving different methods have been applied and recommended.

Foam rolling (FR) via foam roller, one of these methods, has become a common and popular method in many sports settings.

While the popularity and use of the foam rolling method is gradually increasing, in recent years this method has begun to be applied as vibration and included in warming protocols.

The aim of this study is to compare the effects of 6-week vibration and non-vibration foam rolling on neuromuscular control and performance in male soccer players.

Within the scope of initial assessments; knee flexor and extensor muscle strength and Hamstring/Quadriceps muscle strength ratio with the Lafayette manual muscle testing device, flexibility with the sit-and-reach test, dynamic balance with the Y balance test, reaction time with the "Test You Brain Pro System", lower extremity anaerobic power with the Wingate anaerobic power test, agility with the t-test and sprint with the 20-m sprint test will be evaluated.

After the initial assessment, vibration and non-vibration foam rolling methods will be applied to the gluteal, tensor fascia latae, hamstring, quadriceps femoris and gastrocnemius muscles of both lower extremities of the participants in the intervention groups, in addition to the routine warm-up protocol, 3 days a week for a total of 15 minutes a day for 6 weeks. No intervention will be applied to the participants in the control group. This group will continue the routine warm-up protocol.

After the methods applied to the intervention groups for 6 weeks, the initial assessments applied to all participants will be repeated.

Enrollment

36 patients

Sex

Male

Ages

18 to 22 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 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.

Exclusion criteria

  • 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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

36 participants in 3 patient groups

Vibration Foam Rolling Group
Active Comparator group
Description:
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.
Treatment:
Other: Vibration Foam Rolling
Non-Vibration Foam Rolling Group
Active Comparator group
Description:
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.
Treatment:
Other: Non-Vibration Foam Rolling
Control Group
No Intervention group
Description:
No intervention will be applied to the control group. This group will continue the routine warm-up protocol.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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