Effectiveness of Quick Icing (QI) Technique on Strenght of Jump. (QIJ)
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|ClinicalTrials.gov Identifier: NCT04008602|
Recruitment Status : Suspended (COVID-19)
First Posted : July 5, 2019
Last Update Posted : September 16, 2020
|Condition or disease||Intervention/treatment||Phase|
|Muscle Strength||Device: Quick icing Device: Prolonged Cold||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||150 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Triple (Participant, Care Provider, Investigator)|
|Official Title:||Effectiveness of Quick Icing Technique on Force of Jump: Valuation Through a Jump Platform and a Mobile Application.|
|Actual Study Start Date :||July 21, 2019|
|Estimated Primary Completion Date :||December 1, 2020|
|Estimated Study Completion Date :||December 1, 2021|
Active Comparator: Experimental: Quick Icing
Group receiving the application of cold on the ventral side of the thigh (bilaterally) for 30 seconds, using the technique of ice beakers dynamically.
Device: Quick icing
Brief Application of cold, for a period of up to 30 seconds on a body surface which seeks to promote the activation of the nervous system to produce increased excitability.
Other Name: Brief cooling
Active Comparator: Experimental: Prolonged Cold
Group receiving the intervention of "ice bag" for a period of eight minutes n the ventral side of the thigh (bilaterally).
Device: Prolonged Cold
Prolonged application of cold, for at least 5 minutes or more, on a body surface that aims to reduce nervous system activation by reducing the decreased nerve conduction velocity.
No Intervention: Control:
Group that does not receive intervention and that will rest for ten minutes.
- Comparing maximum jump strength changes pre and post application of cold. [ Time Frame: Baseline and 2 hours later (1 session of treatment) ]Force evaluated through movil aplication and jump plataform.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04008602
|Universidad Andrés Bello|
|Santiago de Chile, Las Condes, Chile, 7591538|
|Principal Investigator:||Hernán A de la Barra Ortiz, Mg.||Universidad Andrés Bello|