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Clinical Trials/NCT05868304
NCT05868304CompletedNot Applicable

Dynamic and Isometric Strength Analyses of Lower Extremity Blood Flow Restriction Training: A Randomized Controlled Trial

Cedars-Sinai Medical Center2 sites in 1 country16 target enrollmentStarted: February 8, 2023Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
16
Locations
2
Primary Endpoint
the changes in Force plate measures from baseline to 16 weeks

Study Overview

Brief Summary

The purpose of this research is to determine the effects of low-load blood flow restriction (BFR) training compared to conventional strengthening using dynamic force plate and isometric force frame analyses in healthy subjects.

Detailed Description

The purpose of this research is to determine the effects of low-load blood flow restriction (BFR) training compared to conventional strengthening using dynamic force plate and isometric force frame analyses in healthy subjects. The primary research procedures are:

Subjects will be randomized into either BFR or conventional strengthening groups.

BFR and conventional strengthening programs will be implemented. Force plate and force frame data will be collected at baseline, 4, 6, 8, 12, and 16 weeks.

Subject Population. The study will enroll 18 healthy volunteers. The study includes 6 visits.

The total study duration for each subject is 16 weeks.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Healthy volunteers without history of knee pathology requiring physical therapy or surgery
  • Individuals between 18 and 40 years old

Exclusion Criteria

  • History of venous thromboembolism or other hematologic disorder Pregnant
  • Coronary artery disease, peripheral arterial disease, or hypertension (> 140/90 mmHg)

Outcomes

Primary Outcomes

the changes in Force plate measures from baseline to 16 weeks

Time Frame: Measured at 4,6,8,12 and 16 weeks.

Relative strength index (RSI)

the change in Force plate measures from baseline to 16 weeks

Time Frame: Measured at 4,6,8,12 and 16 weeks.

Displacement

the changes in Force Frame measure from baseline to 16 weeks

Time Frame: Measured at 4,6,8,12 and 16 weeks.

Velocity M/sec

The change in Force plate measures from baseline to 16 weeks

Time Frame: Measured at 4,6,8,12 and 16 weeks.

Power (W)

the changes in Force Frame measures from baseline to 16 weeks

Time Frame: Measured at 4,6,8,12 and 16 weeks.

Force (N)

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Orr Limpisvasti

Principal Investigator

Cedars-Sinai Medical Center

Study Sites (2)

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