Can Blood Flow Restriction Therapy Improve Strength and Cross-Sectional Area for Shoulder External Rotators Better Than Exercise Alone?

Muscle Weakness Clinical Trial

Official title:

Can Blood Flow Restriction Therapy Improve Strength and Muscle Cross-Sectional Area for Shoulder External Rotators Better Than Exercise Alone?

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04596020
• Other study ID #: 2183025
• Status: Recruiting
• Phase: N/A
• Start date: October 10, 2020
• Est. completion date: December 7, 2020

Study information

• Verified date: October 2020
• Source: George Fox University
• Contact: Jason Brumitt, PhD
• Phone: 15045542461
• Email: jbrumitt[@]georgefox.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This 8-week study will investigate whether the application of blood flow restriction (BFR) therapy augments rotator cuff strength in untrained individuals. This is a RCT with subjects randomized to a BFR or non-BFR group. Both groups will do the same training program: 1) first sitting unilateral knee extension and standing unilateral knee curls (w/ or w/o BFR; 4 sets, 30/15/15/15 reps) and 2) scaption and sidelying external rotation (no BFR for either group; 3 sets x 15 reps each).

Description:

This 8-week study will investigate whether the application of blood flow restriction (BFR) therapy augments rotator cuff strength in untrained individuals. This is a RCT with subjects randomized to a BFR or a non-BFR group. Both groups will perform the same training program 2 times a week over 8 weeks with one group performing the lower extremity exercises under occlusion (i.e., BFR applied to the proximal thigh of the dominant leg).

Prior to starting the study the subjects will have their strength assessed by a blinded physical therapist using a hand held dynamometer. The muscles assessed will be the: quadriceps, the hamstrings, the supraspinatus, and the external rotators of the shoulder. Another blinded physical therapist will assess the cross-sectional area of the quadriceps and the supraspinatus tendon using ultrasonography. These tests will be repeated at the conclusion of the study.

Subjects' training weight will be 30% of their 1 repetition max (1RM). 1RM will be determined using hand held dumbbells for the shoulder exercises and machines (knee extension, knee curl machines) for the lower extremity exercises.

Subjects will be randomized to either the BFR or non-BFR group. Subjects in the BFR group will perform the lower extremity exercises under occlusion (i.e., BFR applied to the proximal thigh of the dominant lower extremity). Both groups will perform 4 sets of each lower extremity exercise for 30/15/15/15 reps. After completing the lower extremity exercises the subjects will perform the shoulder exercises (scaption, sidelying external rotation) for 3 sets of 15 repetitions each. The shoulder exercises will not be performed with BFR in either group.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 40
• Est. completion date: December 7, 2020
• Est. primary completion date: December 7, 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Male or female subjects aged 18 and over

Exclusion Criteria:

• Current neck, shoulder (or general upper extremity), and/or thoracic spine pathology;

• Shoulder surgery (or general upper extremity surgery) during the prior 6-month time period;

• Current lower extremity injury and/or having had a lower extremity surgery during the prior 6-month time period;

• Cervical/thoracic spine surgery during the prior 1-year;

• Subject having 1 or more contraindications for BFR training;

• Under the age of 18 years.

Related Conditions & MeSH terms

• Can Blood Flow Restriction Therapy Augments Strength Gains in the Rotator Cuff
• Muscle Weakness

Intervention

Other:
• Blood Flow Restriction Group (exercise with blood flow restriction using a Delfi unit)
Each group performs the same 4 exercises The BFR group will utilize the Delfi BFR unit

Locations

Country	Name	City	State
United States	George Fox University	Newberg	Oregon

Sponsors (1)

Lead Sponsor	Collaborator
George Fox University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Strength Assessment	Strength will be assessed using a hand held dynamometer and traditional manual muscle test positions	Change in Baseline Strength (Newtons) at 8 weeks
Primary	Ultrasonography	Diagnostic ultrasound will be used to measure the cross-sectional area of the quadriceps (specifically the Rectus Femoris) and the tendon of the supraspinatus	Change in Baseline Cross-Sectional Area of the Quadriceps (specifically Rectus Femoris) and the Supraspinatus tendon at 8 Weeks