- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04353219
The Effect of Compression Stockings During Training on Running Performance
Studies that have examined the effects of compression stocking on athlete's performance have been carried out in a single test, i.e., the athlete's was examined during running/riding/jumping with and without the compression stocking.
Yet, using the stocking during all training session and for longer period of time might further enhance the performance. Compression stocking were found to have a positive effect on the athlete' recovery. We hypotheses that if the athlete will train with the stocking on a regular basis and his/her recovery will improve, it will also improve the performance. In addition, the athlete's body may need an adjustment period to use the compression stocking. As such, the advantages of using compression stocking might only be revealed after training with the socks during a period of time and not just performing the tests/competitions with it.
Study Overview
Status
Intervention / Treatment
Detailed Description
All runners will be examined for: demographical parameters, time of 5 Km run, distance of forward jumping with two leg.
The sample will be divided into 2 research group: research group - all training with compression stocking and control group -training without compression stocking. Both groups will continue their training program for 8 weeks according to their coach. A second examination for the same tests at the end of the 8 weeks.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Haifa, Israel
- Haifa University, Department of PHysical Therapy
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Runners with at least 3 years of experience and background in competitions (participated in at least 5 competitions participated).
- Train between 4-5 time per week, for minimum of 40 minutes and a minimum of 8 km per training.
- Running minimum 35 km per week.
Exclusion Criteria:
- Runners who practiced in the past with compression stocking.
- Complains of lower limb pains
- Medical history of lower limb or back surgery.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: DIAGNOSTIC
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: DOUBLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: research group
training program with compression stocking
|
participants will continue their training program as prepared by their coach with compression stocking
Other Names:
|
ACTIVE_COMPARATOR: control group
training program without compression stocking
|
participants will continue their training program as prepared by their coach without compression stocking
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
change from baseline of time running 5 Km
Time Frame: 8 weeks
|
time in minutes of running 5 Km
|
8 weeks
|
change from baseline of forward two legs jump distance
Time Frame: 8 weeks
|
distance of forward jumping in centimeters
|
8 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
change from baseline of average pulse during running
Time Frame: 8 weeks
|
heart pulse along the running
|
8 weeks
|
change from baseline of maximum pulse during running
Time Frame: 8 weeks
|
maximal heart pulse along the running
|
8 weeks
|
Collaborators and Investigators
Sponsor
Publications and helpful links
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
Keywords
Other Study ID Numbers
- 995
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Sharing Time Frame
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
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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