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Positive Cueing in Knee Arthroplasty.

Primary Purpose

Osteoarthritis, Knee, Psychological Stress, Mental Stress

Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Positive cueing in the information video before a primary TKA
Sponsored by
Leiden University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Osteoarthritis, Knee

Eligibility Criteria

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

Inclusion Criteria: 18 years or older end-stage knee osteoarthritis for which participants were scheduled for a TKA sufficient Dutch languages skills to understand the information video able to fill out the questionnaires. Exclusion Criteria: not receiving TKA for osteoarthritis of the knee not sufficient Dutch languages skills to understand the information video not able to fill out the questionnaires.

Sites / Locations

  • LUMC

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Standard information video before primary total knee arthroplasty

Positive cueing in the information video before a primary total knee arthroplasty

Arm Description

Information video (about procedure, complications, rehabilitation) shown to the participants before TKA in the OLVG.

The information video was adapted from the existing standard information video used in OLVG. The concept of positive cueing was applied to the standard video by an expert team including a psychiatrist and clinical psychologist. Illustrations which were incomprehensible or with negative associations were removed. Four rules were followed to use positive cueing: make patients aware that they are able to influence their own recovery process, be descriptive in explanations; objectively describe the performed procedure, name equivalent, not negatively charged feelings, explain why specific steps and actions during the procedure are performed, so the patients understand what is going to happen, do not use medical langue, but use accessible, understandable language instead.

Outcomes

Primary Outcome Measures

Feasibility outcome measure: acceptibility.
The primary feasibility outcome score was the acceptability to participate, assessed with a developed questionnaire. The investigators conducted a questionnaire about the experience of the participants with a Likart scale 1 - 5, existing of 4 questions. A total score of 12 or higher was interpreted as acceptable since the patient seemed have a positive experience according to the questionnaire. As part of the primary outcome measure (acceptibility), we monitored the time it took a patient to participate in the study. The study should not take more than one hour to be acceptable.

Secondary Outcome Measures

Feasibility outcome measure: rate of recruitment
We determined the rate of recruitment by dividing the number of patients included in this study by the number of patients waiting for total knee arthroplasty meeting all inclusion criteria who were scheduled to be seen on the preoperative outpatient clinic appointment.
Feasibility outcome measure: comprehensibility
Do patients understand what is expected of them during the trial. We analyzed comprehensibility for the patients with a developed questionnaire with a cut off point < 9 and by assessing the rate of completion of the questionnaires (number of questions completed). Specific items that were consistently missing from the questionnaires and were not filled out by the patients were noted. Also, patients received one question about whether they thought the information in the video was easy to understand, cut off point < 3.
Feasibility outcome measure:patients' feedback to the current protocol.
After finishing the questionnaire we asked two feedback questions regarding the protocol: what patients thought of participating in the study, and whether they had suggestions to improve the study process. The feedback from the patients were transcribed and similar answers were categorized.

Full Information

First Posted
January 8, 2023
Last Updated
January 26, 2023
Sponsor
Leiden University Medical Center
Collaborators
Onze Lieve Vrouwe Gasthuis, Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
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1. Study Identification

Unique Protocol Identification Number
NCT05703087
Brief Title
Positive Cueing in Knee Arthroplasty.
Official Title
The Effect of Positive Cueing in the Information Video for Patients Undergoing Total Knee Arthroplasty: a Feasibility Study for a Randomized Controlled Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Completed
Study Start Date
September 21, 2021 (Actual)
Primary Completion Date
November 1, 2021 (Actual)
Study Completion Date
November 1, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Leiden University Medical Center
Collaborators
Onze Lieve Vrouwe Gasthuis, Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

4. Oversight

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

5. Study Description

Brief Summary
To the knowledge of the investigators, the feasibility of an RCT assessing the use of positive cueing in an information video for patients undergoing primary TKA is currently unclear. The investigators conducted a feasibility study with the primary objective to assess the acceptability of the randomized controlled trial (RCT) procedure for participating patients. The secondary objective was to evaluate the rate of recruitment, the comprehensibility (do patients understand what is expected of them during the trial) and if there were any adjustments necessary to the design of the study. The outcome of the current feasibility study will be used to determine whether adjustments are required to the design of the RCT before we proceed.
Detailed Description
Even though total knee arthroplasty (TKA) is a cost-effective treatment, 10 - 34% of the patients report pain and discomfort up to two years after the procedure. Preoperative symptoms of anxiety and/or depression (which is present in approximately 10 - 58.6% of TKA patients seem to be related to poor pain coping techniques, which can lead to higher levels of pain up to two years after surgery. Our previous systematic review showed that a reduction of preoperative symptoms of anxiety and depression may lead to a reduction of postoperative pain after TKA. In radiology, anesthesiology, and pediatric departments multiple studies have been performed on reducing the perception of pain with the use of language and hypnosis. This led to the concept of positive cueing. With positive cueing, general language without negative suggestions is used in provided information and instructions about the management of potential discomfort. Correct use of positive cueing has been shown to improve patients' satisfaction and to decrease need for additional treatments (such as blood transfusion) after several medical procedures, whereas use of negative language (warning patients for pain or negative experiences) seems to result in higher pain and anxiety scores. Before TKA, patients are informed about the procedure and the risk of complications. Positive cueing might positively influence perioperative anxiety symptoms and subsequently improve pain after TKA. The investigators plan to conduct a randomized controlled trial (RCT) to address the question whether the use of positive cueing in the information video for patients undergoing a primary TKA, compared to the standard care video, will reduce the level of preoperative symptoms of anxiety and improve pain coping styles. To the knowledge of the reviewers, no previous studies addressed this topic. Hence, the feasibility of an RCT assessing the use of positive cueing in an information video for patients undergoing primary TKA is currently unclear. As such, this feasibility study was conducted with the primary objective to assess the acceptability of the RCT procedure for participating patients. Secondly, the rate of recruitment, the comprehensibility (do patients understand what is expected of them during the trial) and if there were any adjustments necessary to the design of the study were evaluated. The outcome of the current feasibility study will be used to determine whether adjustments are required to the design of the RCT before the investigators proceed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis, Knee, Psychological Stress, Mental Stress

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
A single-center feasibility study. We compared the use of positive cueing in the information video before a primary total knee arthorplasty (TKA) with the standard information video.
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Standard information video before primary total knee arthroplasty
Arm Type
No Intervention
Arm Description
Information video (about procedure, complications, rehabilitation) shown to the participants before TKA in the OLVG.
Arm Title
Positive cueing in the information video before a primary total knee arthroplasty
Arm Type
Experimental
Arm Description
The information video was adapted from the existing standard information video used in OLVG. The concept of positive cueing was applied to the standard video by an expert team including a psychiatrist and clinical psychologist. Illustrations which were incomprehensible or with negative associations were removed. Four rules were followed to use positive cueing: make patients aware that they are able to influence their own recovery process, be descriptive in explanations; objectively describe the performed procedure, name equivalent, not negatively charged feelings, explain why specific steps and actions during the procedure are performed, so the patients understand what is going to happen, do not use medical langue, but use accessible, understandable language instead.
Intervention Type
Behavioral
Intervention Name(s)
Positive cueing in the information video before a primary TKA
Intervention Description
Two weeks before the surgery, in the outpatient clinic (during their preoperative appointment), the pre-surgery information video was shown to the patients. Patients were randomly allocated to either the positive cueing group (intervention) or the standard care group (control) with Castor EDC (14) using a variable block randomization model. Patients did not know whether they watched the adapted video or the standard video.
Primary Outcome Measure Information:
Title
Feasibility outcome measure: acceptibility.
Description
The primary feasibility outcome score was the acceptability to participate, assessed with a developed questionnaire. The investigators conducted a questionnaire about the experience of the participants with a Likart scale 1 - 5, existing of 4 questions. A total score of 12 or higher was interpreted as acceptable since the patient seemed have a positive experience according to the questionnaire. As part of the primary outcome measure (acceptibility), we monitored the time it took a patient to participate in the study. The study should not take more than one hour to be acceptable.
Time Frame
During the preoperative outpatient clinic visit two weeks before surgery. Directly after watching the video's and completing questionnaires.
Secondary Outcome Measure Information:
Title
Feasibility outcome measure: rate of recruitment
Description
We determined the rate of recruitment by dividing the number of patients included in this study by the number of patients waiting for total knee arthroplasty meeting all inclusion criteria who were scheduled to be seen on the preoperative outpatient clinic appointment.
Time Frame
The number of the patients on the waiting list for total knee arthroplasty and the included patients were assessed two weeks before surgery, during the outpatient clinic visit.
Title
Feasibility outcome measure: comprehensibility
Description
Do patients understand what is expected of them during the trial. We analyzed comprehensibility for the patients with a developed questionnaire with a cut off point < 9 and by assessing the rate of completion of the questionnaires (number of questions completed). Specific items that were consistently missing from the questionnaires and were not filled out by the patients were noted. Also, patients received one question about whether they thought the information in the video was easy to understand, cut off point < 3.
Time Frame
During the preoperative outpatient clinic visit two weeks before surgery. Directly after watching the video's and completing questionnaires.
Title
Feasibility outcome measure:patients' feedback to the current protocol.
Description
After finishing the questionnaire we asked two feedback questions regarding the protocol: what patients thought of participating in the study, and whether they had suggestions to improve the study process. The feedback from the patients were transcribed and similar answers were categorized.
Time Frame
During the preoperative outpatient clinic visit two weeks before surgery. Directly after watching the video's and completing questionnaires.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18 years or older end-stage knee osteoarthritis for which participants were scheduled for a TKA sufficient Dutch languages skills to understand the information video able to fill out the questionnaires. Exclusion Criteria: not receiving TKA for osteoarthritis of the knee not sufficient Dutch languages skills to understand the information video not able to fill out the questionnaires.
Facility Information:
Facility Name
LUMC
City
Leiden
ZIP/Postal Code
2333 ZA
Country
Netherlands

12. IPD Sharing Statement

Plan to Share IPD
No

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Positive Cueing in Knee Arthroplasty.

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