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Clinical Trials/CTRI/2024/07/070972
CTRI/2024/07/070972
Not yet recruiting
未知

Effect of Blood Flow Restriction (BFR) Training and Variable Repetition Duration (VRD)Training on Physical Performance Parameters in Fitness Enthusiasts: An Experimental Study - NI

Sarfraznawaz F Shah0 sites0 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Sarfraznawaz F Shah
Status
Not yet recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional

Investigators

Sponsor
Sarfraznawaz F Shah

Eligibility Criteria

Inclusion Criteria

  • Fitness enthusiasts actively engaged in regular exercise or sports activities (e.g.,resistance training, running, cycling, etc.) (150mins/week)
  • \- Participants with no history of cardiovascular or musculoskeletal disorders that would contraindicate BFR training.
  • \- Participants willing to commit to a 6\-week structured training program consisting of BFR and VRD training.
  • \- Participants with no prior experience with BFR training or similar occlusion techniques.
  • \- Ability to understand and follow the study protocols and instructions provided by the research team.
  • \- Willingness to provide informed consent to participate in the study

Exclusion Criteria

  • \- Individuals with a history of cardiovascular diseases, hypertension, or other medical conditions that may pose a risk during BFR training.
  • \- Participants with musculoskeletal injuries or conditions that would limit their ability to perform exercise safely.
  • \- Pregnant or breastfeeding women due to potential risks associated with BFR training.
  • \- Individuals currently using medications or supplements that may affect exercise performance or cardiovascular responses.
  • \- Participants with a known allergy or sensitivity to materials used in BFR cuffs or bands.
  • \- Athletes or individuals participating in high\-intensity training programs that may interfere with the study outcomes.
  • \- Individuals with a history of thrombotic disorders or blood clotting abnormalities.

Outcomes

Primary Outcomes

Not specified

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