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What Matters to Patients With Severe Hip or Knee Osteoarthritis? (PATI-Project)

Primary Purpose

Hip Osteoarthritis, Knee Osteoarthritis

Status
Not yet recruiting
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Shared decision-making supported by an in-consultation PtDA to patients with severe osteoarthritis in their hip or knee
Sponsored by
Vejle Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Hip Osteoarthritis focused on measuring Hip Osteoarthritis, Knee Osteoarthritis, Shared Decision Making, Total knee arthroplasty, Partiel knee arthroplasty, Total hip arthroplasty, Decision quality, HK-DQI

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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)

Sites / Locations

  • Odense University Hospital, OUH
  • Odense University Hospital, OUH
  • Lillebaelt Hospital - Vejle

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Shared decision-making (SDM)

Usual practice

Arm Description

Patients will be informed by a nurse before being consulted by the surgeon randomized to SDM and use the in-consultation PtDA during the consultation on patients with severe hip or knee osteoarthritis

Patients will be informed by a nurse before being consulted by the surgeon randomized to usual practice during the consultation on patients with severe hip or knee osteoarthritis

Outcomes

Primary Outcome Measures

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.

Secondary Outcome Measures

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
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
The participant's pain and physical function after undergoing hip replacement surgery as measured by the Oxford Hip Score (OHS) questionnaire
Oxford Knee Score (OHS): Measuring function and pain with patients undergoing knee replacement surgery. Total scores range from 0 (poorest function) to 48 (maximal function).
The participant's pain and physical function after undergoing knee replacement surgery as measured by 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).
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 ADL. Minimum value: 0. Maximum value: 100. The higher score, the less the patient is aware of their affected joint.
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
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
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.
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.

Full Information

First Posted
June 8, 2023
Last Updated
July 24, 2023
Sponsor
Vejle Hospital
Collaborators
Odense University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05972525
Brief Title
What Matters to Patients With Severe Hip or Knee Osteoarthritis?
Acronym
PATI-Project
Official Title
What Matters to Patients With Severe Hip or Knee Osteoarthritis? Decisional Quality, Patient Involvement and Health Outcome
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
September 11, 2023 (Anticipated)
Primary Completion Date
July 11, 2024 (Anticipated)
Study Completion Date
March 11, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Vejle Hospital
Collaborators
Odense University Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed Description
Osteoarthritis (OA) is the most common joint disease and a major cause of disability worldwide. The condition typically affects the hip or knee, and as the condition progresses it frequently causes debilitating pain and stiffness in the affected joints; thus impairing mobility, and decreasing function and quality of life(QoL). Approximately 10,300 primary hip arthroplasties (THA) and 10,000 primary knee arthroplasties (TKA/UKA) were performed in Denmark in 2021. For the majority of patients with severe osteoarthritis, evidence shows that joint replacement surgery is life-changing. Despite this documented effect, not all patients achieve optimal results. Patient dissatisfaction following THA and TKA has been reported as 7 % and 11-18%, respectively. It is hypothesized that a lack of adequate information and patient involvement in the decision process might lead to the misalignment of patients' expectations and subsequent dissatisfaction. Considerable evidence shows that patients prefer more information and greater involvement. This strongly supports the concept that patients need to be actively involved in treatment decisions. Accordingly, increasing patient involvement in healthcare decisions may be beneficial. Shared decision-making (SDM) supports patients' active involvement in the process and improves the quality of decisions. SDM can be facilitated using a PtDA, which has shown significant benefits in a range of patient groups. However, research on SDM and PtDAs in patients with severe hip or knee OA is lacking. The overall aim of this project is to investigate if an in-consultation PtDA increases the decision quality for patients with severe OA of the hip or knee.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hip Osteoarthritis, Knee Osteoarthritis
Keywords
Hip Osteoarthritis, Knee Osteoarthritis, Shared Decision Making, Total knee arthroplasty, Partiel knee arthroplasty, Total hip arthroplasty, Decision quality, HK-DQI

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The group of hip and knee surgeons at Vejle, Odense, and Svendborg hospitals will be randomized 1:1 either to continue standard consultation or to practice SDM supported by the in-consultation PtDA.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
551 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Shared decision-making (SDM)
Arm Type
Experimental
Arm Description
Patients will be informed by a nurse before being consulted by the surgeon randomized to SDM and use the in-consultation PtDA during the consultation on patients with severe hip or knee osteoarthritis
Arm Title
Usual practice
Arm Type
No Intervention
Arm Description
Patients will be informed by a nurse before being consulted by the surgeon randomized to usual practice during the consultation on patients with severe hip or knee osteoarthritis
Intervention Type
Behavioral
Intervention Name(s)
Shared decision-making supported by an in-consultation PtDA to patients with severe osteoarthritis in their hip or knee
Intervention Description
The intervention group has been involved in the development process of the PtDA. After receiving a training course in SDM and the use of a PtDA, the surgeons will practice SDM supported by an in-consultation PtDA during the consultations with the participant.
Primary Outcome Measure Information:
Title
The participant's decisional quality according to The Hip/Knee Osteoarthritis Decision Quality Instrument (HK-DQI).
Description
Informed Patient-Centered (IPC) decision is calculated as the percentage of patients who are well-informed and received their preferred treatment.
Time Frame
Within one week after inclusion in the consultation
Secondary Outcome Measure Information:
Title
Participant's engagement in the decision-making process as measured by the CollaboRATE questionnaire
Description
Minimum value: 0. Maximum value: 100. The higher the value the more shared decision-making
Time Frame
Within one week after inclusion in the consultation
Title
Participant's involvement in the decision-making process as measured by the HK-DQI questionnaire
Description
HK-DQI, section 3, decision-making process: Minimum value: 0. Maximum value: 100. The higher the value the more shared decision-making
Time Frame
Within one week after inclusion in the consultation
Title
The participant's pain and physical function after undergoing hip replacement surgery as measured by the Oxford Hip Score (OHS) questionnaire
Description
Oxford Knee Score (OHS): Measuring function and pain with patients undergoing knee replacement surgery. Total scores range from 0 (poorest function) to 48 (maximal function).
Time Frame
Three months and one year following surgery
Title
The participant's pain and physical function after undergoing knee replacement surgery as measured by Oxford Knee Score (OKS) questionnaire
Description
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).
Time Frame
Three months and one year following surgery
Title
The participant's physical function after undergoing hip or knee replacement surgery as measured by Forgotten Joint Score (FJS) questionnaire
Description
Forgotten joint score (FJS): Measuring the participants' awareness of their artificial joint during ADL. Minimum value: 0. Maximum value: 100. The higher score, the less the patient is aware of their affected joint.
Time Frame
Three months and one year following surgery.
Title
Participant's Qol when undergoing hip or knee replacement surgery as measured by EuroQol (EQ-5D)
Description
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
Time Frame
Three months and one year following surgery.
Title
The duration of consultation when PtDA is used compared to standard consultation without the use of PtDA.
Description
The time duration will be documented by the surgeons
Time Frame
Through study completion, an average of 1 year
Title
Participant's regret of the treatment decision as measured by the Decision Regret Scale questionnaire.
Description
The Decision Regret Scale: Minimum value: 0. Maximum value: 100. The higher the value the more regret.
Time Frame
Three months and one year following surgery.
Title
Participant's satisfaction after undergoing hip or knee replacement surgery as measured by the patient satisfaction questionnaire (PSQ)
Description
The patient satisfaction questionnaire (PSQ): The higher the value the more satisfaction.
Time Frame
Three months and one year following surgery.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Trine Ahlmann, PhD stud
Phone
+4561164836
Email
trine.alman.pedersen@rsyd.dk
First Name & Middle Initial & Last Name or Official Title & Degree
Claus Varnum, Ass.Prof.MD
Phone
+4579405779
Email
Claus.Varnum@rsyd.dk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Trine Ahlmann, PhD stud
Organizational Affiliation
Vejle Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Claus Varnum, Ass.Prof.MD
Organizational Affiliation
Vejle Hospital
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Martin Lindberg-Larsen, Ass.Prof.MD.
Organizational Affiliation
Odense University Hospital
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Charlotte Myhre Jensen, Ass.Prof.RN
Organizational Affiliation
Odense University Hospital
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Karina Dahl Steffensen, Prof.MD.
Organizational Affiliation
Vejle Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Odense University Hospital, OUH
City
Odense
ZIP/Postal Code
5000
Country
Denmark
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Trine Ahlmann, PhD student
Phone
+4561164836
Email
Trine.Alman.Pedersen@rsyd.dk
Facility Name
Odense University Hospital, OUH
City
Svendborg
ZIP/Postal Code
5700
Country
Denmark
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Trine Ahlmann, PhD student
Phone
+4561164836
Email
Trine.Alman.Pedersen@rsyd.dk
Facility Name
Lillebaelt Hospital - Vejle
City
Vejle
ZIP/Postal Code
7100
Country
Denmark
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Trine Ahlmann, PhD student
Phone
+4561164836
Email
Trine.Alman.Pedersen@rsyd.dk

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
All data of the outcome measures will be available in an anonymized form if required by the scientific journal, in which the results of the trial will be published.
IPD Sharing Time Frame
Data will be available after the publication of the trial
IPD Sharing Access Criteria
Data access will be reviewed by the author's group

Learn more about this trial

What Matters to Patients With Severe Hip or Knee Osteoarthritis?

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