Effectiveness of Foam Rolling on Selected Muscle Groups on Jumping

March 1, 2023 updated by: Charles University, Czech Republic

The Immediate Effect of Posterior Chain Facilitation by Foam Rolling on Reactive Force Performance

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.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

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.

Study Type

Interventional

Enrollment (Actual)

15

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

      • Praha, Czechia
        • Charles University, Faculty of physical education and sport

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

18 years to 30 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Description

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

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: Screening
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: 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.

Foam rolling was performed for 4 minutes with the goal of affecting the entire myofascial posterior chain.
No Intervention: Control group
The control group of probands rested in a resting sitting position for 4 minutes after pre-tests, corresponding to the intervention period.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Angles of inclination of the fuselage to the vertical.
Time Frame: 45 minutes
Measurements were made using video recording (GoPro HERO 9), with 1080p resolution and a recording rate of 240fps. Subsequent analysis of torso tilt was performed in Kinovea, with video frames taken over each obstacle at the moment of greatest torso tilt relative to the vertical axis. Using the marked point above the trochanter major ossis femoris and the external auditory canal outlet, a trunk axis was created and used to measure the angle relative to the vertical axis.
45 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Foot to ground contact time.
Time Frame: 1 hour
The Optojump instrument (Microgate, Bolzano, Italy) was used to acquire the resist phase data by means of laser shadowing. This data was transcribed into OptoJumpNext, from where it was transferred to an excel program and processed there.
1 hour
Jump height.
Time Frame: 45 min
The Optojump (Microgate, Bolzano, Italy) was also used to obtain the jump height data by using the resistance phase time, which is plugged into the formula, to obtain the jump height.
45 min

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Jitka Malá, PhDr, Ph.D., Charles University, Faculty of physical education and sport

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)

January 9, 2023

Primary Completion (Actual)

January 24, 2023

Study Completion (Actual)

January 30, 2023

Study Registration Dates

First Submitted

February 15, 2023

First Submitted That Met QC Criteria

March 1, 2023

First Posted (Actual)

March 13, 2023

Study Record Updates

Last Update Posted (Actual)

March 13, 2023

Last Update Submitted That Met QC Criteria

March 1, 2023

Last Verified

January 1, 2023

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Harasimova foam rolling

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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