NCT04808024

Brief Summary

The aim of the study is to assess the impact of SMR intervention in the hamstring muscles on the activity of the biceps and gluteus muscles.

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
40

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jan 2021

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 4, 2021

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

March 16, 2021

Completed
3 days until next milestone

First Posted

Study publicly available on registry

March 19, 2021

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 21, 2021

Completed
10 days until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2021

Completed
Last Updated

March 19, 2021

Status Verified

March 1, 2021

Enrollment Period

4 months

First QC Date

March 16, 2021

Last Update Submit

March 17, 2021

Conditions

Outcome Measures

Primary Outcomes (3)

  • 1. Surface electromyography (sEMG) examination before SMR

    The sEMG examination of the biceps and gluteus muscles will be performed using the MyoTrace 400 recorder by Noraxon USA Inc. with a sampling frequency of 1000 Hz, using the bipolar method, in accordance with SENIAM standards.The bioelectrical activity of the muscles will be tested during the squat.

    Before the SMR intervention

  • Surface electromyography (sEMG) examination immediately after SMR

    The change in bioelectrical activity of the biceps and gluteus muscles will be performed. The bioelectrical activity of the muscles will be tested during the squat.

    Immediately after the SMR intervention

  • Surface electromyography (sEMG) examination 5 minutes after SMR

    The change in bioelectrical activity of the biceps and gluteus muscles will be performed. The bioelectrical activity of the muscles will be tested during the squat.

    5 minutes after the SMR intervention

Study Arms (2)

Players of amateur football leagues

EXPERIMENTAL

The players of amateur football leagues who will receive SelfMyofascial Release intervention

Procedure: SelfMyofascial Release

Control group

NO INTERVENTION

The players of amateur football leagues who will receive no intervention

Interventions

Myofascial auto-release consisted of rolling the roller on a group of knee flexors for 3.5 minutes between the sciatic tumor and the knee joint in both directions, omitting the popliteal fossa. Before and after the intervention, sEMG of the biceps and gluteal muscles will be performed.

Players of amateur football leagues

Eligibility Criteria

Age18 Years - 40 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • signing informed consent to participate in the study
  • age in the range of 18-40 years

You may not qualify if:

  • people who had orthopedic injuries to the lower limbs and the lumbar-pelvic-iliac complex in the last year
  • people who reported pain in the lower limbs and the lumbar-pelvic-iliac complex on the day of the examination
  • people who underwent myofascial therapy in the last 6 weeks
  • people with non-specific neuromuscular disorders

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department of Kinesitherapy and Special Methods, SHS in Katowice, Medical University of Silesia, Katowice, Poland

Katowice, Silesian Voivodeship, 40-752, Poland

RECRUITING

Study Officials

  • Magdalena Dąbrowska-Galas

    Department of Kinesitherapy and Special Methods, SHS in Katowice, Medical University of Silesia in Katowice, Katowice, Poland

    STUDY DIRECTOR

Central Study Contacts

Tomasz Król

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lecturer at Department of Kinesitherapy and Special Methods, SHS in Katowice, Medical University of Silesia, Katowice, Poland

Study Record Dates

First Submitted

March 16, 2021

First Posted

March 19, 2021

Study Start

January 4, 2021

Primary Completion

April 21, 2021

Study Completion

May 1, 2021

Last Updated

March 19, 2021

Record last verified: 2021-03

Data Sharing

IPD Sharing
Will not share

The datasets used and / or analyzed in the present study will be available from the respective author upon reasonable request.

Locations