Investigation of the Individual Fatigue Response During Blood Flow Restriction Training
Recruiting
N/A
Interventional Study
Total Knee Anthroplasty
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 85
- Sex
- Any
- Study type
- Interventional
- Purpose
- Diagnostic
- Participants needed
- 20 (estimated)
- Sponsor
- University Hospital, Bonn · Other
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About This Trial
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.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Elective TKA caused by osteoarthritis of the knee
* Ability to perform cycling exercise
* Participant of the Rehab center
Exclusion Criteria:
* Open Wounds
* Iatrogenic Vessel Changes (e.g. Bypasses, Stenting)
* Sickle Cell Anemia
Contacts