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Recruiting NCT07043127

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

No phase Interventional Total Hip Arthroplasty (THA)

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Sham-BFR, BFR.
Who it may be relevant to
Registry conditions: Total Hip Arthroplasty (THA). Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Germany
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

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

Overview

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.

Interventions

  • Other Sham-BFR
    The exercise protocol provides for units of approx. 25 minutes of BFR training five times a week as part of medical training therapy. Based on the initial strength measurements prior to rehabilitation, the training phase of the intervention group starts with 30% of the 1RM (calculated from the force-velocity profile) and 70% LOP in the operated leg and 75% of the 1RM (calculated from the force-velocity profile) in the unoperated leg. The patients are randomized into 2 groups: 1) intervention gro
  • Other BFR
    The exercise protocol provides for units of approx. 25 minutes of BFR training five times a week as part of medical training therapy. Based on the initial strength measurements prior to rehabilitation, the training phase of the intervention group starts with 30% of the 1RM (calculated from the force-velocity profile) and 70% LOP in the operated leg and 75% of the 1RM (calculated from the force-velocity profile) in the unoperated leg. The patients are randomized into 2 groups: 1) intervention gro

Primary outcome measures

  • Muscle Strength [Time frame: Pre- (Baseline) to Post-Rehabilitation (after three weeks of outpatient rehabilitation)]
  • Subjective Pain Level [Time frame: Pre- (Baseline) to Post-Rehabilitation (after three weeks of outpatient rehabilitation)]

Eligibility criteria

Inclusion criteria

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

Exclusion criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Other

Study locations

Germany · 1 center
  • University Hospital Bonn — Bonn

Identifiers

NCT: NCT07043127 · 2024_E

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗