Shoulder and Upper Arm InjuryNCT07707960
Blood Flow Restriction on EMG During UQYBT
An observational study of Shoulder and Upper Arm Injury, run by Texas Woman's University at 1 site in United States.
Trial 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. Read more about this study
- Who is it for?
- Ages 18 to 30 yearsHealthy volunteers can take part
- Conditions the study is for
- Shoulder and Upper Arm Injury
- What is being tested?
- Blood flow restriction unit
- Type of treatment
- Medical device
- How many people
- 30 participants
- Where
- 1 siteUnited States
- Study dates
- 1 Jun 2024to 12 Dec 2025
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 30 years
- All sexes
- Healthy volunteers accepted
- Adult
Study population: Healthy adults from 18 to 30 years old
Who may be able to join
- aged 18 to 30 years of age
- able to perform a pushup position for one minute
- able to follow simple commands
Who cannot join
- 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
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Effects of Blood Flow Restriction on Dominant Upper Extremity Electromyography During Upper Quarter Y-Balance Test
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.
Read the 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.
- Conditions
- Shoulder and Upper Arm Injury
- Being tested
- Blood flow restriction unit
- Keywords
- blood flow resistance
- Medical subject headings
- Arm Injuries
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Blood flow restriction unitDevice
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.
| Study group | Role | What they receive |
|---|---|---|
| Cohort performing the Upper Quarter Y-Balance Test with and without BFR applied to their arm | Cohort of 30 healthy participants Receives: Device: Blood flow restriction unit |
What is being measured
The primary outcome is the main question the study is designed to answer.
Electromyography
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.
Measured: 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.
Secondary outcomes (1)
UQYBT Reach Distances
Centimeter reach distances on the UQYBT, which incorporates the UQYBT kit with calibrated length measurements built into the kit.
Measured: 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.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted16 Jul 2026
- Study start1 Jun 2024
- Primary completion12 Dec 2025
- Study completion12 Dec 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Shoulder and Upper Arm InjuryStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 30 participants (actual)
Sponsor and investigators
- Lead sponsor
- Texas Woman's University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Luciano Garcia, Texas Woman's University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07707960
- Sponsor's protocol ID
- TexasWU BFR UQYBT
- Status last verified
- Jul 2026
- First submitted
- 21 Jun 2026
- Last updated
- 16 Jul 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 16 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effects of Blood Flow Restriction on Dominant Upper Extremity Electromyography During Upper Quarter Y-Balance Test
- ClinicalTrials.gov ID
- NCT07707960
- Acronym / sponsor ID
- TexasWU BFR UQYBT
- Conditions
- Shoulder and Upper Arm Injury
- Keywords
- blood flow resistance
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 30 participants (actual)
- Lead sponsor
- Texas Woman's UniversityUniversity, hospital or other
- Study start
- 1 Jun 2024 (actual)
- Primary completion
- 12 Dec 2025 (actual)
- Study completion
- 12 Dec 2025 (actual)
- First posted
- 16 Jul 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Cohort performing the Upper Quarter Y-Balance Test with and without BFR applied to their arm | – | Device: Blood flow restriction unitCohort of 30 healthy participants |
Who may qualify
- Ages
- 18 to 30 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
- Study population
- Healthy adults from 18 to 30 years old
Key inclusion criteria (3 listed)
- aged 18 to 30 years of age
- able to perform a pushup position for one minute
- able to follow simple commands
Key exclusion criteria (3 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Blood flow restriction unitA Delfi PTS (Personal Tourniquet System) unit wrapped around the proximal UE to occlude 50% of blood flow while the participant is performing the trials. | Device | Cohort performing the Upper Quarter Y-Balance Test with and without BFR applied to their arm |
Primary outcome
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.
1 secondary outcome
UQYBT Reach Distances
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.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 16 Jul 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Shoulder and Upper Arm Injury, run by Texas Woman's University at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 16 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
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.). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Jul 2026.