Comparison of Complication Rate, Functional Outcome and Quality of Life Between Standard Therapy Versus Fast-track Therapy in Patients Following Hip Replacement Surgery
The fast track group vs. control group will be compared with regard to hospitalization time and the non-inferiority of the fast track group vs. control group with regard to HOOS will be assessed.
The questionnaires will only be collected in the study: Eq-5d-5l, HOOS, self-efficacy, enjoyment of movement, fear of movement, pain catastrophizing.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* Age ≥18 years
* The patient will undergo surgery at Klinikum rechts der Isar, Technical University of Munich (TUM)
* Written informed consent for participation in the study after detailed explanation of the nature, significance, risks and scope of the clinical trial
* Written informed consent from the patient for data collection and data processing, with the patient fully informed.
* Sufficient German language skills of the patient.
Exclusion Criteria:
* Age \< 18 years
* The patient is under guardianship, legally incapacitated or has limited legal capacity
* Only partial weight-bearing permitted
Primary outcome measure(s)
Hospital length of stay (days) — From day of surgery until discharge, up to 4 days post-surgery The total number of days a participant remains admitted in the hospital from the day of surgery until discharge. While the expected length of stay is approximately 4 days, some participants may stay longer depending on clinical needs.
Hip Disability and Osteoarthritis Outcome Score (HOOS) — From baseline (pre-surgery) to 3 months post-surgery The Hip Disability and Osteoarthritis Outcome Score (HOOS) is a validated, patient-reported instrument for assessing hip-related pain, function, and quality of life.
Scores range from 0 to 100, with higher scores indicating better outcomes (less pain, better function, improved quality of life).
Trial sites (1)
Facility
City
Region
Status
Department Physical Therapy
München
Germany
Recruiting
More Technical University of Munich trials in Germany
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
We use cookies to analyse site traffic and improve your experience. With your consent, we may also use cookies for advertising. You can change your choice at any time.