Knee Replacement Clinical Trials

Clinical trials related to Knee Replacement Procedure

Clinical-randomized Trial of the Effect of Rehabilitation Therapy Using Strength and Blood Flow Restriction Training on Muscular Fitness and Regeneration After Anterior Cruciate Ligament Reconstruction

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

With the intention of improving rehabilitation after anterior cruciate ligament reconstruction, the present project investigates the influence of a targeted strength and blood flow restriction training intervention (BFR training) on the regeneration of muscle mass, strength and functionality of the knee joint. BFR training is characterized by the combination of external venous vascular occlusion with light strength training and still enables users to achieve gains in muscle mass and strength that are comparable to training with high mechanical loads. The positive effects of BFR training in the course of knee arthroplasty have already been demonstrated by our working group as a prehabilitative approach, i.e. as a training intervention prior to surgery. 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. The interventions are carried out as part of the exercise therapy units in outpatient rehabilitation ETM01 in accordance with the S2k guideline on anterior cruciate ligament rupture. Strength and BFR training in medical training therapy supplements the daily exercise therapy to ensure implementation in the rehabilitation process in line with the guidelines.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• ACL reconstruction

• Ability to take part in an outpatient rehabilitation

Locations
Other Locations
Germany
University Hospital Bonn
RECRUITING
Bonn
Contact Information
Primary
Alexander Franz, Dr. med., B.Sc.
alexander.franz@ukbonn.de
+491703750718
Time Frame
Start Date: 2025-06-20
Estimated Completion Date: 2026-12-31
Participants
Target number of participants: 30
Treatments
Active_comparator: Control Group
Control group will perform the exercise protocols with a sham-BFR pressure of 20 mmHg.
Experimental: Intervention Group
Intervention group will perform the exercise protocols with a BFR pressure corresponding to 60% of the individual limb occlusion pressure.
Related Therapeutic Areas
Sponsors
Leads: University Hospital, Bonn

This content was sourced from clinicaltrials.gov