Safety and Effects of High-Intensity Blood Flow Restriction Training in the Rotator Cuff

ConditionHealthy Adult
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorUniversity of Valencia

About this trial

This study aims to analyze the effects of an 8-week strength training program combining different exercise intensities and blood flow restriction (BFR) conditions on safety, tolerability, muscle adaptations, and physical performance variables. Three training modalities will be compared: 1) high-intensity exercise with BFR therapy; 2) low-intensity exercise with BFR therapy; and 3) high-intensity exercise without BFR therapy. All groups will perform the same exercise modality, differing only in intensity and the application of BFR.

Participants will be randomly assigned to one of the three groups and will undergo a 8-week intervention. The variables of interest will be assessed in each group for subsequent analysis and comparison.

Eligibility criteria

Qualifiers

Healthy, untrained adults

Age between 18 and 65

Disqualifiers

Current participation in an upper limb strength training program

Presence of comorbidities that increase cardiovascular risk (uncontrolled ischemic heart disease, uncontrolled hypertension, diabetes, etc.)

Patients with more than one thromboembolism risk factor (obesity, history of thrombosis, prolonged immobilization, recent surgery, use of contraceptives, etc.)

Current diagnosis of any pathology affecting the cervical spine, shoulder, and/or thoracic spine

Trial design

Treatments tested in this trial

  • High-intensity exercise with BFR
  • Low-intensity exercise with BFR
  • High-intensity exercise without BFR

Treatment groups

60 Participants
are divided into 3 treatment groups

Locations

This trial has no locations

Sponsors and collaborators