Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID07043127

Clinical Randomized Trial of Rehabilitation Using Strength and Blood Flow Restriction Training After Elective Hip Replacement

Led by University Hospital, Bonn · Updated on 2025-12-08

30

Participants Needed

1

Research Sites

21 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating whether sports science-controlled strength and blood flow restriction (BFR) training has similar effects on muscular fitness and recovery during outpatient rehabilitation after elective hip replacement surgery. The study compares these methods as part of medical training therapy within a guideline-based rehabilitation process at the Bonn Center for Outpatient Rehabilitation. Participants will be randomized into two groups: one group receives strength training combined with BFR using specific occlusion pressures based on their initial strength measurements, while the control group receives a sham-BFR intervention with a low occlusion pressure. Both groups undergo approximately 25-minute training sessions five times a week during outpatient rehabilitation lasting three weeks. During the study, participants' muscle strength and subjective pain levels will be measured before and after the three-week rehabilitation period. Researchers will assess the effects of the different training interventions on these outcomes. The trial includes double-masked procedures and randomization, with participant involvement focused on outpatient exercise therapy sessions and strength assessments.

CONDITIONS

Brief Title

Impact of Rehabilitation Therapy Using Strength and Blood Flow Restriction Training on Muscular Fitness and Regeneration After Elective Hip Replacement

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Ability for rehabilitation
  • Total hip arthroplasty surgery during the last 4 weeks
  • Age 18 years or older
Not Eligible

You will not qualify if you...

  • Sickle cell anemia
  • Iatrogenic changes in the vessels of the lower extremity (e.g., stents)
  • Open wounds or infections of the lower extremity

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 3 weeks

Participants undergo rehabilitation training with either blood flow restriction (BFR) intervention or sham-BFR as part of their rehabilitation therapy after elective hip replacement.

Approximately 5 sessions per week

Trial Site Locations

Total: 1 location

1

University Hospital Bonn

Bonn, North Rhine-Westphalia, Germany, 53127

Actively Recruiting

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Research Team

A

Alexander Franz, Dr. med., B.Sc.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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