Foam Rolling and Tissue Flossing of the Cuff Muscles

November 2, 2020 updated by: Sebastian Klich, University School of Physical Education in Wroclaw

Foam Rolling and Tissue Flossing of the Cuff Muscles: Acute Effect on Jump Height, Sprint Performance and Achilles Tendon Stiffness

The hypothesis is that self-myofascial release (SMR) intervention on the cuff muscles would affect positively sprint performance and jump height, as well as, decrease Achilles tendon stiffness. The second hypothesis is that tissue flossing would be more effective than foam rolling.

The participants will be randomly assigned to foam rolling, tissue flossing, and control group (without any intervention). After the intervention, repeated measures will be performed (15m sprint, countermovement jump (CMJ) and Achilles tendon stiffness). This will aim to improve sprint time, jump height and decrease tendon stiffness.

Study Overview

Status

Completed

Detailed Description

Foam rolling provides beneficial results in ankle range of motion, muscle flexibility or muscle sourness. Tissue flossing is popular in athletic training and physical therapy, as an effective strategy for ankle range of motion or performance. However, there is a lack of knowledge about the use of foam rolling and tissue flossing during a 60 minutes post-intervention examination on the performance and soft tissue stiffness.

The main aim of this study is to investigate the effect of foam rolling and tissue flossing of the cuff on sprint performance, jump height and Achilles tendon stiffness at different time points. The second aim is to assess the effectiveness of those self-myofascial release methods (SMR).

This study will include healthy, recreational active subjects aged between 20 and 25 years old.

Study Type

Interventional

Enrollment (Actual)

60

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

    • Lower Silesia
      • Wrocław, Lower Silesia, Poland, 51-612
        • University Team Sport Hall

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

20 years to 25 years (ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Regular physical exercise activity (~3 times per week).

Exclusion Criteria:

  • Experience with the application of foam rolling and tissue flossing.
  • Current or prior pain or injury in the lower extremity.
  • Previous history of surgery in the lower extremity.
  • Cardiovascular disabilities.

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: PARALLEL
  • Masking: DOUBLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Foam rolling
Foam rolling of cuff muscles.
Foam rolling performed on cuff muscles in 3 sets of 30 seconds per each muscle part in duration with a 15-second rest between sets. The first sets on the central part of the cuff muscles, the second on the medial and third on the lateral side of the cuff.
EXPERIMENTAL: Tissue flossing
Tissue flossing of cuff muscles.
A standard cuff muscle bandaging technique on cuff muscle. After the application, each participant is asked to perform a 2 min ankle-exercise program.
NO_INTERVENTION: Control group
Without any intervention.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in counter-movement jump (CMJ)
Time Frame: Baseline, 5 minutes, 15 minutes, 30 minutes, 45 minutes, 60 minutes
A maximum vertical jump with counter-movement.
Baseline, 5 minutes, 15 minutes, 30 minutes, 45 minutes, 60 minutes
Change in 15-meter sprint run
Time Frame: Baseline, 5 minutes, 15 minutes, 30 minutes, 45 minutes, 60 minutes
The 15-meter sprint involves a participant starting behind a timing gate and running through a second timing gate 15 meters away.
Baseline, 5 minutes, 15 minutes, 30 minutes, 45 minutes, 60 minutes
Change in viscoelastic properties of the Achilles tendon.
Time Frame: Baseline, 5 minutes, 15 minutes, 30 minutes, 45 minutes, 60 minutes
Stiffness measured on (1) Achilles tendon origin, (2) Achilles tendon on the center ankle joint, and (3) intermuscular septum between medial and lateral head of the gastrocnemius muscle.
Baseline, 5 minutes, 15 minutes, 30 minutes, 45 minutes, 60 minutes

Collaborators and Investigators

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

Investigators

  • Study Director: Adam Kawczyński, Prof., University School of Physical Education in Wrocław

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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)

September 7, 2020

Primary Completion (ACTUAL)

October 9, 2020

Study Completion (ACTUAL)

October 16, 2020

Study Registration Dates

First Submitted

April 22, 2020

First Submitted That Met QC Criteria

April 24, 2020

First Posted (ACTUAL)

April 29, 2020

Study Record Updates

Last Update Posted (ACTUAL)

November 3, 2020

Last Update Submitted That Met QC Criteria

November 2, 2020

Last Verified

November 1, 2020

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • USPEWroclaw
  • 26/2016 (OTHER: University School of Physical Education in Wroclaw)

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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