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临床试验/NCT07344740
NCT07344740尚未招募不适用

Blood Flow Restriction Resistance Exercise and Cardiac Cycle Dynamics

Montclair State University1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2026年2月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
40
试验地点
1
主要终点
Cardiac cycle durations

研究概览

简要总结

Blood flow restriction resistance exercise uses partial vascular occlusion of a limb during low weight resistance exercises to stimulate muscle strengthening and growth. This is commonly used during rehabilitation from an injury. Because blood flow in and out of the limbs is decreased, this may have consequences for blood flow through the heart. The purpose of this study will be to test cardiac dynamics during blood flow restriction resistance exercise to determine if cardiac blood flow is impacted. It is hypothesized that both non-BFR exercise and BFR exercise will increase heart rate shortening various cardiac cycle parameters, but BFR exercise will increase the isovolumetric contraction time vs non-BFR exercise due to an increase in total peripheral resistance. It is also hypothesized that BFR exercise will lower early ventricular filling parameters due to lower venous return.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Generally healthy

排除标准

  • Uncontrolled hypertension
  • Peripheral vascular disease
  • Lymphedema
  • Sickle cell anemia
  • Heart failure
  • Stroke history
  • Heart attack history
  • Rheumatoid arthritis
  • Chronic kidney disease
  • Severe neuropathy
  • Any condition that may make blood flow restriction resistance exercise riskier like history of blood clots
  • Use of coagulant therapy
  • Susceptible to blood clots

研究组 & 干预措施

Intervention group

Experimental

Blood flow restriction resistance exercise

干预措施: Blood flow restriction resistance exercise (Behavioral)

结局指标

主要结局

Cardiac cycle durations

时间窗: During the intervention for approximately 10 minutes.

Ventricular filling

时间窗: During intervention phase for approximately 10 minutes.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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