NCT05764837

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
15

participants targeted

Target at below P25 for not_applicable hypertension

Timeline
Completed

Started Jan 2023

Shorter than P25 for not_applicable hypertension

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 9, 2023

Completed
15 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 24, 2023

Completed
6 days until next milestone

Study Completion

Last participant's last visit for all outcomes

January 30, 2023

Completed
16 days until next milestone

First Submitted

Initial submission to the registry

February 15, 2023

Completed
26 days until next milestone

First Posted

Study publicly available on registry

March 13, 2023

Completed
Last Updated

March 13, 2023

Status Verified

January 1, 2023

Enrollment Period

15 days

First QC Date

February 15, 2023

Last Update Submit

March 1, 2023

Conditions

Keywords

SMRplyometricsjumps over hurdlesposterior myofascial chain

Outcome Measures

Primary Outcomes (1)

  • Angles of inclination of the fuselage to the vertical.

    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 Outcomes (2)

  • Foot to ground contact time.

    1 hour

  • Jump height.

    45 min

Study Arms (2)

Intervention group

EXPERIMENTAL

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.

Other: Foam Rolling

Control group

NO INTERVENTION

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

Interventions

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

Intervention group

Eligibility Criteria

Age18 Years - 30 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • 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

You may not qualify if:

  • injuries
  • acute illnesses
  • chronic disease
  • musculoskeletal limitations
  • during convalescence

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Charles University, Faculty of physical education and sport

Prague, Czechia

Location

MeSH Terms

Conditions

Hypertension

Condition Hierarchy (Ancestors)

Vascular DiseasesCardiovascular Diseases

Study Officials

  • Jitka Malá, PhDr, Ph.D.

    Charles University, Faculty of physical education and sport

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
SCREENING
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 15, 2023

First Posted

March 13, 2023

Study Start

January 9, 2023

Primary Completion

January 24, 2023

Study Completion

January 30, 2023

Last Updated

March 13, 2023

Record last verified: 2023-01

Data Sharing

IPD Sharing
Will not share

Locations