The Immediate Physiological and Perceptual Response to Blood-flow Restricted Strength Training With Eccentric Loading
E-BFR
2 other identifiers
interventional
48
1 country
1
Brief Summary
Decreasing workloads in strength training makes it more tolerable for a broad range of people. When designed as blood-flow restriction training, similar gains in strength and muscle mass are achieved compared to traditional training. Adding high training loads to blood-flow restriction training only in the eccentric phase (BFR-ECC) might achieve superior gains in muscle strength while still maximizing tolerability of the training stimuli. This study aims to investigate the acute physiological and perceptual response of blood-flow restriction training with eccentric loading in comparison to traditional eccentric training. The study recruits healthy individuals ≥ 18 years.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable healthy
Started Jan 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 31, 2025
CompletedFirst Submitted
Initial submission to the registry
February 6, 2025
CompletedFirst Posted
Study publicly available on registry
March 4, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 28, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
July 28, 2025
CompletedJuly 31, 2025
July 1, 2025
6 months
February 6, 2025
July 28, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
minute ventilation
recorded with breath-by-breath analysis
During the intervention (i.e., exercise) for 10 minutes
Secondary Outcomes (5)
Other variables from breath-by-breath analysis
During the intervention (i.e., exercise) for 10 minutes
Rate of perceived exertion
Immediately after the intervention (i.e., exercise)
Near-infrared spectroscopy of the vastus lateralis
During the intervention (i.e., exercise) for 10 minutes
Delayed onset muscle soreness
24, 48, and 72 hours after each of the intervention (i.e., exercise)
Feasibility and tolerability
After study completion (i.e., after the second study visit, up to 2 weeks)
Study Arms (2)
Eccentric blood-flow restriction trainig
EXPERIMENTALEccentric free-flow training
ACTIVE COMPARATORInterventions
Eccentric blood-flow restriction training
Eligibility Criteria
You may qualify if:
- Clinically Healthy
You may not qualify if:
- Physical or intellectual impairment precluding informed consent or protocol adherence
- Pain during exercise of any origin
- History of thromboembolic event in the lower extremity
- Known pregnancy (no testing is carried out)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Zurich
Zurich, 8001, Switzerland
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
February 6, 2025
First Posted
March 4, 2025
Study Start
January 31, 2025
Primary Completion
July 28, 2025
Study Completion
July 28, 2025
Last Updated
July 31, 2025
Record last verified: 2025-07