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Clinical Trials/NCT07707960
NCT07707960CompletedNot Applicable

Effects of Blood Flow Restriction on Dominant Upper Extremity Electromyography During Upper Quarter Y-Balance Test

Texas Woman's University1 site in 1 country30 target enrollmentStarted: June 1, 2024Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
30
Locations
1
Primary Endpoint
Electromyography

Study Overview

Brief Summary

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.

Detailed Description

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.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 30 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • aged 18 to 30 years of age
  • able to perform a pushup position for one minute
  • able to follow simple commands

Exclusion Criteria

  • no spine, upper extremity, or lower extremity pain
  • no spine, upper extremity, or lower extremity surgery or disorder in the past six months
  • no blood clotting or vascular disorder which would make BFR harmful

Outcomes

Primary Outcomes

Electromyography

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.

Secondary Outcomes

  • UQYBT Reach Distances(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.)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Luciano Garcia

Assistant Professor

Texas Woman's University

Study Sites (1)

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