- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04841733
Effectiveness of Recovery Protocols Combination in Soccer Players
April 18, 2021 updated by: University of Vic - Central University of Catalonia
Evaluation of the Effectiveness of the Combination of Different Post-effort Recovery Methods on Quality and Recovery Time in Semi-professional Soccer Players
The main objective of this project is to compare the effectiveness of combining different recovery methods on perceptual and physical performance on soccer players.
Study Overview
Status
Enrolling by invitation
Conditions
Intervention / Treatment
Detailed Description
A crossover study will be performed and players will be assigned to different recovery methods combinations after their participation in a football game.
The investigators will take baseline measures before the game and post-competition measures 24 hours after the game (one hour before the recovery intervention).
Moreover, another two measure moments will be used, 24 and 48 hours after the recovery intervention.
Study Type
Interventional
Enrollment (Anticipated)
20
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
-
-
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Vic, Spain, 08500
- Universitat de Vic-Universitat Central de Catalunya
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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
16 years and older (Child, Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- semi-professional soccer players
- 75 minutes game participation (minimum)
- 5 years of experience practicing soccer
Exclusion Criteria:
- goalkeepers
- injured players
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: Non-Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Protocol I: Foam Roller (FR) + Cold-Water Immersion (CWI)
Foam Roller (FR) Cold-Water Immersion (CWI)
|
Foam Roller (FR): participants will follow the Foam Roller protocol using a polyvinylchloride pipe roller (10.3-cm diameter, 0.3-cm thickness surrounded by a 1,5-cm thickness neoprene foam).
They will begin with the Foam Roller at the most proximal portion of the muscle and to roll as much body mass as tolerable back and forth along it as smoothly as possible at a cadence of 1 second superior and 1 second inferior as determined with the metronome.
Foam Roller will be performed for 45 seconds followed by a 15-second rest for each muscle group (quadriceps, adductors, hamstrings, abductors and calf) in each extremity and repeated once.
Cold-Water Immersion (CWI): will be the last strategy used.
Participants will immerse their lower body to the level of the hips for 10 minutes in cold water (10° C).
|
Experimental: Protocol II: Stretching (STR) + Cold-Water Immersion (CWI)
Stretching (STR) Cold-Water Immersion (CWI)
|
Cold-Water Immersion (CWI): will be the last strategy used.
Participants will immerse their lower body to the level of the hips for 10 minutes in cold water (10° C).
Stretching (STR): participants will perform 8-min of static stretching, involving 3 bilateral repetitions of 30 seconds held stretches to the quadriceps, adductors, hamstrings, abductors and calf muscles.
|
Experimental: Protocol III: Foam Roller (FR) + Stretching (STR)
Foam Roller (FR) Stretching (STR)
|
Foam Roller (FR): participants will follow the Foam Roller protocol using a polyvinylchloride pipe roller (10.3-cm diameter, 0.3-cm thickness surrounded by a 1,5-cm thickness neoprene foam).
They will begin with the Foam Roller at the most proximal portion of the muscle and to roll as much body mass as tolerable back and forth along it as smoothly as possible at a cadence of 1 second superior and 1 second inferior as determined with the metronome.
Foam Roller will be performed for 45 seconds followed by a 15-second rest for each muscle group (quadriceps, adductors, hamstrings, abductors and calf) in each extremity and repeated once.
Stretching (STR): participants will perform 8-min of static stretching, involving 3 bilateral repetitions of 30 seconds held stretches to the quadriceps, adductors, hamstrings, abductors and calf muscles.
|
Experimental: Protocol IV: Foam Roller (FR) + Stretching (STR) + Cold-Water Immersion (CWI)
Foam Roller (FR) Stretching (STR) Cold-Water Immersion (CWI)
|
Foam Roller (FR): participants will follow the Foam Roller protocol using a polyvinylchloride pipe roller (10.3-cm diameter, 0.3-cm thickness surrounded by a 1,5-cm thickness neoprene foam).
They will begin with the Foam Roller at the most proximal portion of the muscle and to roll as much body mass as tolerable back and forth along it as smoothly as possible at a cadence of 1 second superior and 1 second inferior as determined with the metronome.
Foam Roller will be performed for 45 seconds followed by a 15-second rest for each muscle group (quadriceps, adductors, hamstrings, abductors and calf) in each extremity and repeated once.
Cold-Water Immersion (CWI): will be the last strategy used.
Participants will immerse their lower body to the level of the hips for 10 minutes in cold water (10° C).
Stretching (STR): participants will perform 8-min of static stretching, involving 3 bilateral repetitions of 30 seconds held stretches to the quadriceps, adductors, hamstrings, abductors and calf muscles.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Neuromuscular or physical performance measures change: jump height
Time Frame: Baseline, 1 hour before intervention, 24 hours after intervention, 48 hours after intervention
|
Counter Movement Jump (CMJ) will be performed to determine the maximum height in centimeters (cm).
From standing position with the hands fixed on the hips, participants will be required to bend their knees to a freely chosen angle and perform a maximal vertical jump.
Participants will be instructed to keep their body vertical throughout the jump, and to land with knees fully extended.
Any jump that will be perceived to deviate from the required instructions will be repeated.
Players will jump 3 times as high as possible and the best attempt will be used in subsequent analysis.
A 15-s passive recovery phase will be provided between jumps.
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Baseline, 1 hour before intervention, 24 hours after intervention, 48 hours after intervention
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Neuromuscular or physical performance measures change: jump flight and contact time
Time Frame: Baseline, 1 hour before intervention, 24 hours after intervention, 48 hours after intervention
|
Counter Movement Jump (CMJ) will be performed to determine the jump flight and contact time in milliseconds (ms).
From standing position with the hands fixed on the hips, participants will be required to bend their knees to a freely chosen angle and perform a maximal vertical jump.
Participants will be instructed to keep their body vertical throughout the jump, and to land with knees fully extended.
Any jump that will be perceived to deviate from the required instructions will be repeated.
Players will jump 3 times as high as possible and the best attempt will be used in subsequent analysis.
A 15-s passive recovery phase will be provided between jumps.
|
Baseline, 1 hour before intervention, 24 hours after intervention, 48 hours after intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Subjective perceptual/well-being questionnaire measures change
Time Frame: Baseline, 1 hour before intervention, 24 hours after intervention, 48 hours after intervention
|
The well-being questionnaire (McLean et al. 2010) will assess participants' fatigue, sleep quality, general muscle soreness, stress levels and mood on a five-point scale (scores of 1[worst outcome] to 5 [best outcome], 0.5 point increments).
Overall well-being will then be determined by summing the five scores.
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Baseline, 1 hour before intervention, 24 hours after intervention, 48 hours after intervention
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Total Quality Recovery perceived (TQRper) scale. Subjective perceptual questionnaire measures change
Time Frame: Baseline, 1 hour before intervention, 24 hours after intervention, 48 hours after intervention
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Players will be asked to rate their recovery using the subjective questionnaire Total Quality Recovery perceived (TQRper) scale (Kenttä & Hassmén, 1998) answering the question "how recovered you feel?" on a scale which ranges from 0 (very poorly recovered) to 10 (very well recovered) and it's used as a subjective measurement to assess the fatigue suffered by the players (Laurent et al., 2011).
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Baseline, 1 hour before intervention, 24 hours after intervention, 48 hours after intervention
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Rate of Perceived Exertion (RPE) scale. Subjective perceptual questionnaire measures change
Time Frame: Baseline, 1 hour before intervention, 24 hours after intervention, 48 hours after intervention
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Players will be asked to rate their rate of perceived exertion using Rate of Perceived Exertion (RPE) Borg's scale answering the question "how exhausted do you feel?" on a scale which ranges from 0 (extremely well-rested) to 10 (extremely exhausted) (Casamichana et al., 2013).
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Baseline, 1 hour before intervention, 24 hours after intervention, 48 hours after intervention
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Albert Altarriba-Bartes, UVic-UCC
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.
General Publications
- Laurent CM, Green JM, Bishop PA, Sjokvist J, Schumacker RE, Richardson MT, Curtner-Smith M. A practical approach to monitoring recovery: development of a perceived recovery status scale. J Strength Cond Res. 2011 Mar;25(3):620-8. doi: 10.1519/JSC.0b013e3181c69ec6.
- McLean BD, Coutts AJ, Kelly V, McGuigan MR, Cormack SJ. Neuromuscular, endocrine, and perceptual fatigue responses during different length between-match microcycles in professional rugby league players. Int J Sports Physiol Perform. 2010 Sep;5(3):367-83. doi: 10.1123/ijspp.5.3.367.
- Kentta G, Hassmen P. Overtraining and recovery. A conceptual model. Sports Med. 1998 Jul;26(1):1-16. doi: 10.2165/00007256-199826010-00001.
- Casamichana D, Castellano J, Calleja-Gonzalez J, San Roman J, Castagna C. Relationship between indicators of training load in soccer players. J Strength Cond Res. 2013 Feb;27(2):369-74. doi: 10.1519/JSC.0b013e3182548af1.
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)
April 18, 2021
Primary Completion (Anticipated)
September 1, 2021
Study Completion (Anticipated)
October 1, 2021
Study Registration Dates
First Submitted
April 8, 2021
First Submitted That Met QC Criteria
April 8, 2021
First Posted (Actual)
April 12, 2021
Study Record Updates
Last Update Posted (Actual)
April 20, 2021
Last Update Submitted That Met QC Criteria
April 18, 2021
Last Verified
April 1, 2021
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- RCTREC002
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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