- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04689698
The Effect of Flossing to Joint Range of Motion.
Influence of Flossing Tape Therapy on the Range of Motion and Influencing of Fascial Chains in the Lower Limbs
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Methodology:
The weight-bearing lunge test (WBLT) was used to evaluate the change in the ankle joint's range of motion. A simple forward bend test - the Thomayer test - was used to evaluate the therapy's effect on the Superficial fascial backline described by Myers. Both tests are non-invasive. Both tests can be used to evaluate the outcome of a given therapy objectively. Both tests are elementary to perform and highly standardized and commonly used in similar research.
After completing the entrance tests, the tissue flossing method is applied to each proband. The treatment alone does not typically last more than 20 minutes for any proband. As part of the tissue flossing treatment, both lower limbs of the proband will be treated. The "tissue flossing" method will be applied according to the authors' standard recommendations first to the plantar fascia area, then to the ankle joint. Finally, the last treated structure will be the area of fascia cruris. The duration of each application does not exceed 2 minutes. The order of individual applications is determined in advance as follows: right and then left plantar fascia, right and then left ankle joint and right and then left fascia cruris. Each application will be supplemented by the standard manual treatment or supplemented by the proband's active movement. After a total of 6 treatments, the therapeutic unit will be finished, and each proband will be re-examined using the same tests as before the treatment. If a given proband experiences any undesirable complications during the application of the "tissue flossing" method or applying the given method to the proband is subjectively unpleasant, the given treatment will be finished immediately.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Praha, Czechia
- Charles University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- No previous experience with the tissue flossing method
- Each proband had to do recreational or elite sports
Exclusion Criteria:
- persons with an acute, especially infectious disease, person with an injury or persons in the process of recovery after an injury or illness
- vascular diseases
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: experimental group
|
Testing of the ankle in sagittal line and Thomayer test before and after flossing of sole.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Measurement of range of motion of ankle in sagital line
Time Frame: 5 minutes
|
Measurement without flossing of sole in natura
|
5 minutes
|
Measurement of range of motion of ankle in sagital line
Time Frame: 15 minutes
|
Flossing of sole and than measurement after flossing of sole
|
15 minutes
|
Measurement of range of motion of lumbar spine in sagital line
Time Frame: 5 minutes
|
Measurement before flossing of sole
|
5 minutes
|
Measurement of range of motion of lumbar spine in sagital line
Time Frame: 15 minutes
|
Measurement after flossing of sole
|
15 minutes
|
Collaborators and Investigators
Investigators
- Principal Investigator: Jitka Malá, PhDr.Ph.D., Charles University, Faculty of physical education and sport
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Pisarčík, Flossing
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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