- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05094713
Effects of Muscle Flossing on Quadriceps Muscle Potentiation (MF_TMG_CMJ)
October 25, 2022 updated by: Science and Research Centre Koper
Effects of Tissue Flossing on Muscle Contractile Properties and Jumping Performance in Recreationally Active Students
Tissue flossing involves wrapping a thick rubber band around a joint or muscle, which can partially occlude blood flow.
In practice, it is often used while concomitantly performing a range of motion exercises (ROM) for 1 to 3 minutes in duration.
The mechanisms involved in tissue flossing with a floss band may be similar to those involved in ischemic preconditioning.
Previous results would support the use of tissue flossing on ROM, while there are no clear conclusions on post-activation effects on sports-related performance and muscle contractile properties.
This may be attributed to the different methodologies used in the studies.
Therefore, the time course associated with tissue flossing benefits remains to be investigated.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Nowadays, various methods are used for acute performance enhancement.
The most recent of these is tissue flossing, which is becoming increasingly popular for both performance enhancement and rehabilitation.
However, the effects of flossing on athletic performance have not been clearly demonstrated, which could be due to differences in the methodology used.
In particular, the rest periods between the end of the preconditioning activity and the performance of the criterion task or assessment tools varied considerably in the published literature.
Therefore, the present study aimed to investigate the effects of applying tissue flossing to the thigh on bilateral countermovement jump performance and contractile properties of vastus lateralis (VL) muscle.
Nineteen recreational athletes (11 males; aged 23.1 ± 2.7 years) were randomly assigned to days of flossing application (3 sets for 2 min of flossing with 2 min rest between sets) with preset experimental pressure (EXP = 95 ± 17.4 mmHg) or control condition (CON = 18.9 ± 3.5 mmHg).
The first part of the measurements was performed before and after warm-up consisting of 5 min of cycling followed by dynamic stretching and specific jumping exercises, while the second part consisted of six measurement points after flossing application (0.5, 3, 6, 9, 12, 15 min).
Study Type
Interventional
Enrollment (Actual)
19
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
-
-
-
Koper, Slovenia, 6000
- Science and Research Centre Koper
-
-
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
18 years to 35 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Healthy and physically active individuals
- without a history of lower limb injuries and/or surgeries at least 1 year prior to investigation.
Exclusion Criteria:
- neuromuscular and metabolic disorders;
- the presence of acute and/or chronic pain
- alcohol and drug consumption etc.
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: Basic Science
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Flossing - control
Control group where flossing wrapping pressure is between 20 and 30 mmHg
|
Control group where flossing wrapping pressure is between 20 and 30 mmHg
Other Names:
|
|
Experimental: Flossing with medium wrapping pressure
A flossing band will be applied over tight musculature with medium wrapping pressure
|
Flossing of the tight muscles with medium wrapping pressure, which is individualized in based on the tight circumference of the participant.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Contractile muscle properties
Time Frame: 75 min
|
Contractile muscle properties assessed using tensiomyography (Tc, Dm, Tr, Ts, Td)
|
75 min
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
CMJ jump height
Time Frame: 75 min
|
Counter-movement jump height assessed using force plate
|
75 min
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Rate of perceived exertion
Time Frame: 75 min
|
Rate of perceived exertion of fatigue
|
75 min
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Armin Paravlic, PhD, SRC Koper and Faculty of Sport
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.
Helpful Links
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)
July 20, 2021
Primary Completion (Actual)
October 1, 2021
Study Completion (Actual)
October 15, 2021
Study Registration Dates
First Submitted
October 13, 2021
First Submitted That Met QC Criteria
October 13, 2021
First Posted (Actual)
October 26, 2021
Study Record Updates
Last Update Posted (Actual)
October 27, 2022
Last Update Submitted That Met QC Criteria
October 25, 2022
Last Verified
October 1, 2022
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- MFPAP
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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