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Study identifier: NCT07394582 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Preoperative Optimization Before Total Hip or Knee Replacement Surgery

Condition: Prehabilitation · Preoperative Care  ·  Sponsor: Medical University Innsbruck

PhaseNA
Planned participants180
Who can joinAll sexes, 18 Years to 99 Years
Healthy volunteersNo

About this study

Preoperative Optimisation prior to Hip and Knee Arthroplasty (PrOpE) Many patients scheduled for planned hip or knee replacement surgery have health conditions that may affect recovery, such as reduced physical fitness, nutritional problems, multiple medications, or increased stress and anxiety. These factors can increase the risk of complications and delay recovery after surgery. The PrOpE study examines whether a structured preparation programme before surgery, known as preoperative optimization or prehabilitation, can be safely implemented and may support recovery after hip or knee replacement. Aim of the study The main aim is to assess the feasibility of a comprehensive preoperative optimisation programme and to explore its potential effects on recovery and health outcomes. The results will help improve future care for patients undergoing major orthopaedic surgery. Who can participate? Adult patients scheduled for elective total hip or knee replacement surgery who are classified as ASA \>2, aged between 18 and 99 years old and without a severe cognitive impairment. Participation is voluntary. Study design A total of 180 participants will be included and randomly assigned to one of two groups: • Standard Care Group: Participants receive usual medical care before and after surgery. • Intervention Group: In addition to standard care, participants receive an individualised preparation programme over several weeks before surgery. This programme may include: * Personal…

This description comes directly from the study's public registry record.

Talk to the study team

Helmut Raab, MD  ·  +435050480833  ·  helmut.raab@tirol-kliniken.at

Christine Eckhardt, MD, PhD  ·  christine.eckhardt@i-med.ac.at

Always discuss trial participation with your own doctor first.

Locations (1)

Medical University InnsbruckInnsbruck, Tyrol, AustriaRecruiting

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Source record: clinicaltrials.gov/study/NCT07394582