- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05764837
Effectiveness of Foam Rolling on Selected Muscle Groups on Jumping
The Immediate Effect of Posterior Chain Facilitation by Foam Rolling on Reactive Force Performance
Study Overview
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
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Praha, Czechia
- Charles University, Faculty of physical education and sport
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
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
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.
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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.
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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
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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.
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45 minutes
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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.
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1 hour
|
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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.
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45 min
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Collaborators and Investigators
Investigators
- Principal Investigator: Jitka Malá, PhDr, Ph.D., Charles University, Faculty of physical education and sport
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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