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临床试验/NCT07043127
NCT07043127招募中不适用

Clinical Randomized Trial of the Influence of Rehabilitation Therapy Using Strength and Blood Flow Restriction Training on Muscular Fitness and Regeneration After Elective Hip Replacement

University Hospital, Bonn1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2025年1月1日最近更新:
适应症
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
30
试验地点
1
主要终点
Subjective Pain Level

研究概览

简要总结

In the present project, the framework conditions of outpatient rehabilitation at the Bonn Center for Outpatient Rehabilitation will now be used to prove whether sports science-controlled strength and BFR training has a similar effect in the postoperative rehabilitation phase. Strength and BFR training in medical training therapy complements daily exercise therapy in order to ensure implementation in the guideline-based rehabilitation process. . The interventions are carried out as part of the exercise therapy units in outpatient rehabilitation ETM01 following the RTS hip and knee TEP basis KTL 2020.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Double (Participant, Outcomes Assessor)

入排标准

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

入选标准

  • •Ability for Rehabilitation
  • •Total Hip Arthroplasty Surgery during the last 4 Weeks

排除标准

  • •Sickle Cell Anemia
  • •Iatrogenic changes in the vessels of the lower Extremity (e.g. Stents)
  • •Open Wounds or Infections of the lower Extremity

研究组 & 干预措施

Control Group

Active Comparator

Regular Rehabilitation Training

干预措施: Sham-BFR (Other)

Intervention Group

Experimental

BFR-Intervention during Rehabilitation Training

干预措施: BFR (Other)

结局指标

主要结局

Subjective Pain Level

时间窗: Pre- (Baseline) to Post-Rehabilitation (after three weeks of outpatient rehabilitation)

Visual analog scale (0-100mm)

Muscle Strength

时间窗: Pre- (Baseline) to Post-Rehabilitation (after three weeks of outpatient rehabilitation)

Muscle Strength will be assessed by isometric maximal contraction test on a leg press machine

次要结局

未报告次要终点

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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