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Effectiveness of Foam Rolling on Selected Muscle Groups on Jumping

C

Charles University, Czech Republic

Status

Completed

Conditions

Hypertension

Treatments

Other: Foam Rolling

Study type

Interventional

Funder types

Other

Identifiers

NCT05764837
Harasimova foam rolling

Details and patient eligibility

About

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.

Full 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.

Enrollment

15 patients

Sex

Female

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Screening

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

15 participants in 2 patient groups

Intervention group
Experimental group
Description:
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.
Treatment:
Other: Foam Rolling
Control group
No Intervention group
Description:
The control group of probands rested in a resting sitting position for 4 minutes after pre-tests, corresponding to the intervention period.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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