Comparison of Complication Rate, Functional Outcome and Quality of Life Between Standard Therapy Versus Fast-track Therapy in Patients Following Hip Replacement Surgery

NCT07199751 | Recruiting

• 1 other identifier: 2025-155-S-CB
• Study Type: observational
• Target: 90
• Locations: 1 country
• Sites: 1

Brief Summary

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.

Conditions

Coxarthrosis

Keywords

enhanced recovery; physiotherapy

Outcome Measures

Primary Outcomes (2)

• Hospital length of stay (days)

  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.

  From day of surgery until discharge, up to 4 days post-surgery

• Hip Disability and Osteoarthritis Outcome Score (HOOS)

  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).

  From baseline (pre-surgery) to 3 months post-surgery

Secondary Outcomes (8)

• Timed Up and Go (TUG) Test

  From baseline (pre-surgery) to 3 months post-surgery

• EQ-5D-5L (EuroQol 5 Dimensions, 5 Levels)

  From baseline (pre-surgery) to 3 months post-surgery

• Range of Motion (ROM) - Neutral Zero Method (degrees)

  From baseline (pre-surgery) to 3 months post-surgery

• Exercise Self-Efficacy Scale (ESES)

  From baseline (pre-surgery) to 3 months post-surgery

• Pain Catastrophizing Scale (PCS)

  From baseline (pre-surgery) to 3 months post-surgery

Study Arms (2)

Fast Track

enhanced Recovery

standard therapy

standard therapy

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Hip arthroplasty elective

You may qualify if:

• 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.

You may not qualify if:

• Age \< 18 years
• The patient is under guardianship, legally incapacitated or has limited legal capacity
• Only partial weight-bearing permitted

Sponsors & Collaborators

• Technical University of Munich: lead

Study Sites (1)

Department Physical Therapy

München, 81675, Germany

RECRUITING

MeSH Terms

Conditions

Osteoarthritis, Hip

Condition Hierarchy (Ancestors)

Osteoarthritis; Arthritis; Joint Diseases; Musculoskeletal Diseases; Rheumatic Diseases

Study Officials

• Rüdiger von Eisenhart-Rothe, Prof. Dr.

  Department of Orthopedics and Sports Orthopedics

  STUDY DIRECTOR

Central Study Contacts

Barbara Vogel, Dr.

CONTACT

0049 41408917; Barbara.vogel@mri.tum.de

Study Design

• Study Type: observational
• Observational Model: OTHER
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Dr. rer. biol. hum.

Study Record Dates

• First Submitted: July 7, 2025
• First Posted: September 30, 2025
• Study Start: June 1, 2025
• Primary Completion: December 31, 2025
• Study Completion: December 31, 2025
• Last Updated: September 30, 2025

Record last verified: 2025-09

Data Sharing

• IPD Sharing: Will not share

Locations

DE (1)