High-Load, Low-Load, and Passive Blood Flow Restriction in Competitive Sprinters
Recruiting
N/A
Interventional Study
Blood Flow Restriction
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 – 30
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 18 (estimated)
- Sponsor
- Riphah International University · Other
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About This Trial
This randomized clinical trial will include competitive male and female sprinters aged 16-30 years, recruited through purposive sampling. Participants will be randomly assigned to one of three groups: (A) HL-BFR (70-85% 1RM with BFR during sets), (B) LL-BFR (20-30% 1RM with BFR), or (C) Passive BFR (BFR applied between sets). The intervention will consist of a 6-week sprint-specific resistance tra…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Age between 16-30 years
* Competitive sprinters with at least 2 years of sprint-specific training
* Healthy individuals without cardiovascular, metabolic, musculoskeletal, or neurological disorders
* Willingness to participate in a 6-week training program
Exclusion Criteria:
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Contacts