Acute Effects of Tissue Flossing on Muscle Properties and Jump Performance in Handball

December 13, 2025 updated by: Charles University, Czech Republic

Acute Effects of Tissue Flossing on the Viscoelastic Properties of the Muscles and Jump Performance in Handball Players: a Crossover Design

Purpose of the Study This study looked at how two popular warm-up techniques-tissue flossing and foam rolling-affect muscle flexibility, muscle properties, and jumping ability in young male handball players. The goal was to see which method might be better for preparing athletes for performance.

What Are These Techniques?

Tissue flossing: Wrapping a special elastic band tightly around a muscle or joint for a short time while moving. This temporarily reduces blood flow, and when the band is removed, blood rushes back in, which may boost muscle readiness.

Foam rolling: Using your body weight to roll muscles over a firm foam cylinder. This applies pressure to the muscle and fascia, helping to relax tight areas and increase flexibility.

Who Took Part? 30 male handball players, around 17 years old, who were healthy and injury-free. None had regularly used tissue flossing or foam rolling before.

How Was the Study Done?

Each player tried all three conditions on separate days:

Tissue flossing

Foam rolling

Control (no special technique, just exercises)

Before and after each session, the researchers measured:

Active range of motion (AROM) - how far they could move their leg muscles without help

Muscle properties - stiffness and tone of key thigh muscles

Jump performance - height and speed of force production in a countermovement jump

Measurements were taken before, 2 minutes after, and 15 minutes after each warm-up.

Study Overview

Status

Completed

Conditions

Study Type

Interventional

Enrollment (Actual)

30

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

      • Prague, Czechia, 261 01
        • Faculty of Physical Education and Sport at Charles University

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

  • Child
  • Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Self-identified male
  • Aged approximately 16-18 years
  • Active handball player with at least 8 years of playing experience
  • Currently healthy with no injuries in the past 3 months
  • Able to perform physical activity and complete all testing procedures
  • No prior regular use of tissue flossing (TF) or foam rolling (FR) techniques

Exclusion Criteria:

  • Current or recent (within 3 months) musculoskeletal injury
  • Any medical condition that would limit safe participation in exercise testing
  • Previous experience with tissue flossing (TF) or regular use of foam rolling (FR)
  • Inability to follow study instructions or complete all sessions

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: Other
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Tissue Flossing conditioning
Tissue flossing using a 5 cm x 3.5 m green Sanctband Comprefloss band was wrapped around the thigh area. After the floss band was applied, the participants did 10 bodyweight squats, making sure to bend their knees to a 90-degree angle. Next, they did 10 dynamic lunges on each leg, switching legs after each lunge. After finishing these exercises, the floss band was removed.
Tissue flossing using a 5 cm x 3.5 m green Sanctband Comprefloss band was wrapped around the thigh area. After the floss band was applied, the participants did 10 bodyweight squats, making sure to bend their knees to a 90-degree angle. Next, they did 10 dynamic lunges on each leg, switching legs after each lunge. After finishing these exercises, the floss band was removed.
Experimental: Foam rolling conditioning
Each participant rolled the quadriceps on the right, then the left, for 30 seconds each, and did the same for the hamstrings, starting with the right and then the left, also for 30 seconds each side.
Using a firm foam roller to roll the quadriceps and hamstrings for 30 seconds per side.
No Intervention: No intervention
Participants perform standard dynamic warm-up exercises (bodyweight squats and lunges) with no additional device or treatment.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Active Range of Motion
Time Frame: Before the intervention, 2 minutes after, and 15 minutes after the intervention.
Measured using the Active Knee Extension (AKE) test for both legs to assess hamstring flexibility.
Before the intervention, 2 minutes after, and 15 minutes after the intervention.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Jump Performance - Jump Height
Time Frame: Before the intervention, 2 minutes after, and 15 minutes after the intervention.
Height achieved in a countermovement jump (CMJ) without arm swing, measured with a force plate.
Before the intervention, 2 minutes after, and 15 minutes after the intervention.
Jump Performance - Braking Rate of Force Development
Time Frame: Before the intervention, 2 minutes after, and 15 minutes after the intervention.
The rate at which force is developed during the braking phase of the CMJ, measured via force plate.
Before the intervention, 2 minutes after, and 15 minutes after the intervention.

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Viscoelastic Muscle Properties - Stiffness
Time Frame: Before the intervention, 2 minutes after, and 15 minutes after the intervention.
Muscle stiffness of the rectus femoris (RF), vastus lateralis (VL), and biceps femoris (BF) in both legs, measured with the MyotonPRO device
Before the intervention, 2 minutes after, and 15 minutes after the intervention.
Viscoelastic Muscle Properties - Tone
Time Frame: Before the intervention, 2 minutes after, and 15 minutes after the intervention
Muscle tone (oscillation frequency) of the RF, VL, and BF in both legs, measured with the MyotonPRO device.
Before the intervention, 2 minutes after, and 15 minutes after the intervention

Collaborators and Investigators

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

February 10, 2023

Primary Completion (Actual)

June 3, 2023

Study Completion (Actual)

June 3, 2023

Study Registration Dates

First Submitted

August 15, 2025

First Submitted That Met QC Criteria

December 13, 2025

First Posted (Actual)

December 29, 2025

Study Record Updates

Last Update Posted (Actual)

December 29, 2025

Last Update Submitted That Met QC Criteria

December 13, 2025

Last Verified

August 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • 177/2020

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

De-identified individual participant data (IPD) that underlie the results reported in this article will be made available upon reasonable request to the corresponding author (anna.pisz@ftvs.cuni.cz). Data will be available immediately following publication, with no end date.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL

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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