- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04630951
Blood Flow Restriction Strength Training in Professional Soccer Players
Effects of Blood Flow Restriction Resistance Training on Muscle Characteristics, Strength and Performance of Professional Soccer Players
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
PARTICIPANTS:
Participants are soccer players of RCD Mallorca (Second Spanish Football Division) and RCD Mallorca B (Third Spanish Football Division).Before to start the study, every participant will receive an informed consent about the clinical study. This informed consent will be signed by them according to Declaration of Helsinki. At the same time, the data will be anonymized and only the main researcher of the study will have access to it, to ensure compliance with the Data Protection Law.
W-UP:
The warm-up will consist of 5 minutes running slow (treadmill), 5 minutes mobility, and 5 minutes of running exercises. In addition, the warm-up will contain a familiarization with the jump test
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Balearic Islands
-
Palma De Mallorca, Balearic Islands, Spain, 07122
- Christian
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- No injuries in the last 6 months
- 1 years experience minimun in the division.
Exclusion Criteria:
- Amateurs players
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Strength training based on low loads with blood flow restriction (Experimental group I)
|
Low Load (20-50% 1RM), 4 set of 30/15/15/15 repetitions, 30 seconds resting between sets.
|
|
Experimental: Strenght training based on high loads (Experimental group II)
|
High Load (60-80% 1RM) 4 sets of 8 repetitions, 2 minutes resting between sets
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from Baseline in Muscle Mass
Time Frame: Change from Baseline in Muscle Mass at 6 Weeks
|
Muscle Mass mesured with measuring tape
|
Change from Baseline in Muscle Mass at 6 Weeks
|
|
Change from Baseline in Maximum Voluntary Isometric Contraction (MVIC)
Time Frame: Change from Baseline in Maximum voluntary Isometric Contraction at 6 Weeks
|
MVIC mesured by Force Platform (Vald Performance, Brisbane, QLD)
|
Change from Baseline in Maximum voluntary Isometric Contraction at 6 Weeks
|
|
Change from Baseline in Electrical Muscle Activity
Time Frame: Change from Baseline in Electrical Muscle Activity at 6 weeks
|
Electrical Muscle Activity mesured by Surface Electromyography (mDurance®, España)
|
Change from Baseline in Electrical Muscle Activity at 6 weeks
|
|
Change from Baseline in Countermovement Jump (CMJ)
Time Frame: Change from Baseline in countermovement Jump (CMJ Test) at 6 weeks
|
CMJ Test measured by Force Platform (Vald Performance, Brisbane, QLD)
|
Change from Baseline in countermovement Jump (CMJ Test) at 6 weeks
|
|
Change from in Force-Velocity Profile (F-V)
Time Frame: Change from Baseline in Force-Velocity Profile at 6 Weeks
|
F-V Profile measured by MyJump App
|
Change from Baseline in Force-Velocity Profile at 6 Weeks
|
|
Change from Baseline in Sprint Ability
Time Frame: Change from Baseline in Sprint Ability at 6 weeks
|
Sprint Ability measured by MySprint App
|
Change from Baseline in Sprint Ability at 6 weeks
|
|
Change from Post-Intervention in Sport Injuries Incidence
Time Frame: Change from Post-Intervention up to 8 months.
|
Incidence of injuries related to sport practice
|
Change from Post-Intervention up to 8 months.
|
Collaborators and Investigators
Investigators
- Principal Investigator: Christian Castilla López, University of Balearic Islands
- Study Director: Natalia Romero Franco, University of Balearic Islands
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 (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 160CER20
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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