Texas Woman's University
Houston, Texas, 77030, United States
NCT Number: NCT07707960
This study will help determine if blood flow restriction (BFR) changes muscle activity on people performing single arm support while reaching with the opposite arm.
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Notify Me18 year–30 year
All sexes
Observational
Houston, Texas, 77030, United States
This study will determine the muscular activation effects of blood flow restriction (BFR) on healthy subjects while they are performing the upper quarter y-balance test (UQYBT) with their dominant arm in stance.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
A Delfi PTS (Personal Tourniquet System) unit wrapped around the proximal UE to occlude 50% of blood flow while the participant is performing the trials.
Time frame: Data will be collected on a single day only. Each subject will only have data collection on one single day. The time frame will be only one hour from the start of data collection to the end. No follow up trials or data collection.
UE and scapular EMG using Delsys Electromyography Unit with Trignio electrodes on the lower trapezius, serratus anterior, anterior deltoid, biceps brachii, and extensor carpi radialis brevis.
Time frame: Data will be collected on a single day only. Each subject will only have data collection on one single day. The time frame will be only one hour from the start of data collection to the end. No follow up trials or data collection.
Centimeter reach distances on the UQYBT, which incorporates the UQYBT kit with calibrated length measurements built into the kit.
Texas Woman's University
Other
Effects of Blood Flow Restriction on Dominant Upper Extremity Electromyography During Upper Quarter Y-Balance Test
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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