osteoarthritis, arthritis, total hip prosthesis, total knee prosthesis
Conditions
Interventions
The investigational product is the standard procedure (usual clinical care) for total hip replacement or total knee replacement.
Sponsors
LUMC, Leiden
Rijnland Ziekenhuis, Leiderdorp
Diaconessenhuis, Leiden
Groene hart ziekenhuis, Leiden
Lange land ziekenhuis, Zoetermeer
Eligibility
Inclusion criteria
Inclusion criteria: 1. All patients who are scheduled for primary total hip or total knee surgery or revision surgery; 2. Are able to complete questionnaires, either on paper or electronically; 3. Patients > 18 years of age.
Exclusion criteria
Exclusion criteria: 1. No informed consent signed; 2. Insufficient Dutch language skills; 3. Physical or mental status not allowing participation.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Knee or hip functioning (HOOS/KOOS); 2. Physical activity (SQUASH questionnaire, accelerometer); 3. Work status; 4. Quality of life (SF-12 and EQ-5D); 5. Patient satisfaction; 6. Health care usage; 7. Radiological outcome (post-operative femorotibial angle (knee) and alignment of the stem and inclination of the cup (Hip) and post-operative complications. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Sociodemographic characteristics (age, sex); 2. Comorbidities (comorbidity questionnaire, Charnley classification and ASA classification); 3. Frailty (>70 years of age: Groningen Frailty Index); 4. Pre-operative use of pharmacological and non-pharmacological treatment for hip or knee pain; 5. Outcome expectations (the New York Hospital for Special Surgery Questionnaire); 6. Preoperative radiographic damage (Kellgren score, Femorotibial angle and alignment of the stem and inclination of the cup) and hand grip strength. | — |
Contacts
Public ContactC. Tilbury
Postzone J11R Postbus 9600
Outcome results
None listed