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临床试验/NCT07611526
NCT07611526招募中不适用

Investigation of the Individual Fatigue Response During Blood Flow Restriction Training on a Cycle Ergometer Following Orthopedic Surgical Interventions

University Hospital, Bonn1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2026年6月26日最近更新:
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
20
试验地点
1

研究概览

简要总结

The aim of the present pilot study is to investigate the feasibility of an exercise pressure response approach for assessing physiological strain during BFR training in a clinically supervised setting. Patients undergoing rehabilitation following total knee arthroplasty (TKA) will be included. The results are intended to contribute to an improved evaluation of load management during BFR training.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Diagnostic
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Elective TKA caused by osteoarthritis of the knee
  • Ability to perform cycling exercise
  • Participant of the Rehab center

排除标准

  • Open Wounds
  • Iatrogenic Vessel Changes (e.g. Bypasses, Stenting)
  • Sickle Cell Anemia

研究组 & 干预措施

High Load

Experimental

High Load (HL-BFR) The second group will perform cycle ergometer training with BFR at a higher individual intensity (60% of heart rate reserve [HRR]) as the first session. One week later, the patients will complete the second exercise session using the protocol of the "LL-BFR" group.

干预措施: Cycling BFR (Device)

Low Load

Experimental

Low Load (LL-BFR) The first group will perform cycle ergometer training with BFR at a low individual intensity (40% of heart rate reserve [HRR]) as the first session. One week later, the patients will complete the second exercise session using the protocol of the "HL-BFR" group.

干预措施: Cycling BFR (Device)

研究者

发起方
University Hospital, Bonn
申办方类型
Other
责任方
Principal Investigator
主要研究者

Alexander Franz

Dr. med., B.Sc.

University Hospital, Bonn

研究点 (1)

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