Effectiveness of Foam Rolling on Selected Muscle Groups on Jumping

NCT ID: NCT05764837

Last Updated: 2023-03-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

15 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-01-09

Study Completion Date

2023-01-30

Brief Summary

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An experiment elucidating the immediate effect of foam rolling of the posterior chain on reactive force performance that will represent multiple jumps over low obstacles. The measurements will be performed using the Optojump device, which will provide data on the time of foot contact with the ground and the jump height. The angles of the torso inclination to the vertical will also be measured during jumping.

Detailed Description

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Fifteen women were selected for this experiment in the form of a randomized crossover study. Measurements were taken by leg jumps over 5 obstacles 125 cm apart. The pre-test was performed twice with a two-minute rest between each trial. Immediately after finishing the second trial, a randomly selected half of the probands performed posterior chain facilitation using a foam roller, facilitating first the left leg, then the right leg and finally spinal erectors. Rolling was performed with a sense of maximal intensity and at a high rolling speed across the full length and width of the muscle with both cranial and caudal rolling directions. Facilitation was performed on each muscle group in the distoproximal direction. Immediately following the intervention, a post-test was performed a total of 3 times, 1 minute after the intervention, 3 minutes after the intervention and 5 minutes after the intervention. The control measurement was performed the same way as the intervention, but the control group of probands rested in a resting sitting position for 4 minutes instead of foam rolling. After one week, a second measurement followed, where the original control group underwent the intervention measurement and vice versa.

The Optojump instrument (Microgate, Bolzano, Italy) was used to obtain the resistance and flight phase data. A video recording (GoPro HERO 9) was taken of the skipping procedure, from which photographs were taken over each obstacle at the moment of the greatest trunk tilt (the junction of the trochanter major and the external auditory canal exit) from the vertical axis.

Conditions

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Hypertension

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

SCREENING

Blinding Strategy

NONE

Study Groups

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Intervention group

Facilitation of the posterior chain was performed by foam rolling (BLACKROLL, standard hardness), where the left lower limb was rolled first, then the right lower limb and finally the spinal erectors. Rolling was performed with a sense of the highest intensity and at a high rolling speed, across the full length and width of the muscle with both cranial and caudal rolling directions. Facilitation was performed on each muscle group in the distoproximal direction, in the order of:

m. triceps surae, hamstrings, and m. gluteus maximus, with the proband attending to each muscle group for 30 s. Finally, bilateral facilitation of mm. erectores spinae in the lumbar and thoracic segments was performed, also for 30 s. The frequency of rolling was determined using a metronome at 1.5 Hz.

Group Type EXPERIMENTAL

Foam Rolling

Intervention Type OTHER

Foam rolling was performed for 4 minutes with the goal of affecting the entire myofascial posterior chain.

Control group

The control group of probands rested in a resting sitting position for 4 minutes after pre-tests, corresponding to the intervention period.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Foam Rolling

Foam rolling was performed for 4 minutes with the goal of affecting the entire myofascial posterior chain.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* women
* age range 18-30 years
* regular training at least 3 times a week
* training with a minimum duration of 1.5 hours
* valid medical sports examination
* experience with jumping over hurdles
* having a problem with maintaining the physiological position of the torso when running

Exclusion Criteria

* injuries
* acute illnesses
* chronic disease
* musculoskeletal limitations
* during convalescence
Minimum Eligible Age

18 Years

Maximum Eligible Age

30 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Charles University, Czech Republic

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Jitka Malá, PhDr, Ph.D.

Role: PRINCIPAL_INVESTIGATOR

Charles University, Faculty of physical education and sport

Locations

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Charles University, Faculty of physical education and sport

Prague, , Czechia

Site Status

Countries

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Czechia

Other Identifiers

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Harasimova foam rolling

Identifier Type: -

Identifier Source: org_study_id

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