Knee Osteoarthritis Clinical Trial
— PATI-ProjectOfficial title:
What Matters to Patients With Severe Hip or Knee Osteoarthritis? Decisional Quality, Patient Involvement and Health Outcome
This clinical trial aims to investigate if shared decision-making, and the use of an in-consultation patient decision aid (PtDA), increases the decisional quality and therefore treatment satisfaction and outcome of patients with severe hip or knee osteoarthritis. Finally, an evaluation will be conducted on patient-reported outcomes on pain, physical function, quality of life (QoL), and patient satisfaction, up to one year after surgery.
Status | Recruiting |
Enrollment | 551 |
Est. completion date | July 11, 2026 |
Est. primary completion date | October 11, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Severe primary osteoarthritis eligible for primary total hip arthroplasty (THA) / primary total knee arthroplasty (TKA) / primary partial knee arthroplasty (UKA) - Able to understand and read Danish - Informed consent Exclusion Criteria: - Previous THA, TKA, or UKA on the contralateral side - Cognitive impairment - Non-OA-related reason for the visit - No digital mailbox (E-boks) |
Country | Name | City | State |
---|---|---|---|
Denmark | Odense University Hospital, OUH | Odense | |
Denmark | Odense University Hospital, OUH | Svendborg | |
Denmark | Lillebaelt Hospital - Vejle | Vejle |
Lead Sponsor | Collaborator |
---|---|
Vejle Hospital | Odense University Hospital |
Denmark,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Participant's Qol when undergoing hip or knee replacement surgery as measured by EuroQol (EQ-5D) | QoL: EuroQol (EQ-5D): Measuring the health-related quality of life. Presenting in three levels; Level 1: Indicating no problem, to Level 3: Indicating extreme problems | Three months and one year following surgery. | |
Other | The participant's pain and physical function after undergoing hip replacement surgery as measured by the Oxford Hip Score (OHS) questionnaire | Oxford Hip Score (OHS): Measuring function and pain with patients undergoing hip replacement surgery. Total scores range from 0 (poorest function) to 48 (maximal function). | Three months and one year following surgery | |
Other | The participant's pain and physical function after undergoing knee replacement surgery as measured by the Oxford Knee Score (OKS) questionnaire | Oxford Knee Score (OKS): Measuring function and pain with patients undergoing knee replacement surgery. Total scores range from 0 (poorest function) to 48 (maximal function). | Three months and one year following surgery | |
Other | The participant's physical function after undergoing hip or knee replacement surgery as measured by Forgotten Joint Score (FJS) questionnaire | Forgotten joint score (FJS): Measuring the participants' awareness of their artificial joint during activity of daily living (ADL). Minimum value: 0. Maximum value: 100. The higher score, the less the patient is aware of their affected joint. | Three months and one year following surgery. | |
Other | Participant's regret of the treatment decision as measured by the Decision Regret Scale questionnaire. | The Decision Regret Scale: Minimum value: 0. Maximum value: 100. The higher the value the more regret. | Three months and one year following surgery. | |
Other | Participant's satisfaction after undergoing hip or knee replacement surgery as measured by the patient satisfaction questionnaire (PSQ) | The patient satisfaction questionnaire (PSQ): The higher the value the more satisfaction. | Three months and one year following surgery. | |
Primary | The participant's decisional quality according to The Hip/Knee Osteoarthritis Decision Quality Instrument (HK-DQI). | Informed Patient-Centered (IPC) decision is calculated as the percentage of patients who are well-informed and received their preferred treatment. | Within one week after inclusion in the consultation | |
Secondary | Participant's engagement in the decision-making process as measured by the CollaboRATE questionnaire | Minimum value: 0. Maximum value: 100. The higher the value the more shared decision-making | Within one week after inclusion in the consultation | |
Secondary | Participant's involvement in the decision-making process as measured by the HK-DQI questionnaire | HK-DQI, section 3, decision-making process: Minimum value: 0. Maximum value: 100. The higher the value the more shared decision-making | Within one week after inclusion in the consultation | |
Secondary | The duration of consultation when PtDA is used compared to standard consultation without the use of PtDA. | The time duration will be documented by the surgeons | Through study completion, an average of 1 year |
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