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CompletedNCT04540367

Blood Flow Restriction Training for The Shoulder

Blood Flow Restriction Training for The Shoulder: A Case for Proximal Benefit

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
69 (actual)
Sponsor
The Methodist Hospital Research Institute · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

The aim of this study is to determine if BFR-LIX promotes greater increases in shoulder lean mass, rotator cuff strength, endurance, and acute increases in shoulder muscle activation compared to LIX alone.

Detailed description

Healthy Volunteers: Thirty-two healthy adults were randomized into two groups (BFRm=13,f=3, NoBFRm=10,f=6) that performed 8wks of shoulder LIX \[2/wk, 4 sets (30/15/15/fatigue), 20%max\] using common rotator cuff exercises \[cable external rotation (ER), cable internal rotation (IR), dumbbell scaption (SCAP), and side-lying dumbbell ER (SLER)\]. The BFR group also trained with an automated tourniquet placed at the proximal arm (50%-occlusion). Regional lean mass (dual-energy-xray-absorptiometry), isometric strength, and muscular endurance (repetitions-to-fatigue, RTF, 20%max, with and without 50%-occlusion) was measured before and after training. Electromyographic amplitude (EMGa) was also recorded from target shoulder muscles during endurance testing. A mixed-model ANCOVA (covaried on baseline measures) was used to detect within and between-group differences in primary outcome measures (α=0.05). Pitchers: Twenty-eight collegiate baseball pitchers were randomized into 2 groups (BFRN=15, NOBFRN=13) that, in conjunction with offseason training, performed 8wks of shoulder LIX \[Throwing arm only; 2/wk, 4 sets (30/15/15/fatigue), 20%isometric max\] using 4 exercises \[cable external and internal rotation (ER/IR), dumbbell scaption, and side-lying dumbbell ER\]. The BFR group also trained with an automated tourniquet on the proximal arm (50%-occlusion). Regional lean mass (dual-energy x-ray absorptiometry), rotator cuff strength (dynamometry: IR0\&90, ° ER0\&90, ° Scaption, Flexion), and fastball biomechanics were assessed pre- and post-training. Achievable workload (sets × reps × resistance) was also recorded. An ANCOVA (covaried on baseline measures) repeated on training timepoint was used to detect within-group and between-group differences in outcome measures (α=0.05). For significant pairwise comparisons, effect size (ES) was calculated using a Cohen's d statistic and interpreted as: 0-0.1, negligible(N); 0.1-0.3, small(S); 0.3-0.5, moderate(M); 0.5-0.7, large(L); \>0.7, very large(VL).

Conditions

Interventions

TypeNameDescription
DEVICEBlood flow restriction therapyThe study group underwent the same exercises as the control group modified by the use of a tourniquet for blood flow restriction during those exercises.

Timeline

Start date
2017-11-10
Primary completion
2020-08-01
Completion
2020-08-01
First posted
2020-09-07
Last updated
2024-08-09
Results posted
2024-08-09

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT04540367. Inclusion in this directory is not an endorsement.