Simultaneous Physiotherapy and Orthopedic Surgeon Interdisciplinary Care
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Enrollment
- 30
- Primary Endpoint
- Change in Oxford Knee Score Questionnaire
Study Overview
Brief Summary
This study will test a protocol to implement simultaneous physiotherapy and orthopedic surgeon interdisciplinary care for patients undergoing knee replacement surgery. These interdisciplinary sessions will help tailor personalized goals, involving the patient as a key member of the team.
Detailed Description
The purpose of this project is to test a quality improvement protocol to improve outcomes following knee arthroplasty surgery utilizing simultaneous physiotherapy and orthopedic surgeon interdisciplinary care. In an era of increasing demands on health care budgets, it is vital to improve quality of care without substantially increasing its cost. This study will focus on a quality improvement strategy that aims to redeploy existing resources to achieve higher quality care without substantially altering costs. This interdisciplinary approach involves establishing a high functioning team that includes the patient as a pivotal member and builds collaboration in the pre-operative period that can be leveraged in the post-operative period to achieve optimal outcomes. This differs from traditional, siloed care for knee arthroplasty.
Participants will be involved in usual care surrounding knee arthroplasty which includes education sessions and pre-habilitation pre-operatively and rehabilitation post-operatively. Participants will also attend two interdisciplinary sessions at 2 months and 1 month prior to surgery to outline expectations, explore patients' questions and concerns, set expectations for the next interdisciplinary session, and ensure goal congruence between all members of the team. At each of these sessions a physical assessment will also be completed by the orthopedic surgeon and physiotherapist. Following surgery, participants will attend four more interdisciplinary sessions at 2 weeks, 6 weeks, 3 months, and 6 months post-operatively. These sessions will address safety and medical issues, revisit patient expectations, reinforce care team expectations, focus on a personalized rehabilitation plan, and ensure goal congruence between the various team members. The physical assessment will also be repeated.
The objectives of the study are as follows:
- Evaluate the feasibility (e.g., recruitment and retention, administrative and participant burden, lived experiences) of treating knee arthroplasty patients through a novel interdisciplinary program aimed to optimize recovery among patients; and
- Estimate the size of the program's effect on biopsychosocial outcomes among community-dwelling individuals undergoing knee arthroplasty and rehabilitation.
The hypotheses of the study are as follows:
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Intervention Model
- Single Group
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Ages
- 19 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •19 years of age or older
- •Expecting to undergo knee arthroplasty surgery within 12 months
- •Pain or functional limitation due to the musculoskeletal condition
- •Able to walk 10 meters without physical assistance
- •Able to tolerate 50 minutes of activity (including rest breaks, as needed)
- •Have adequate cognitive-communicative ability to participate (based on clinical judgment of the research team)
- •Able to provide informed consent
Exclusion Criteria
- •Are living in long-term care
- •Have significant neurological conditions
- •Are medically unstable
- •Have medical condition(s) significantly impacting lower extremity function
Outcomes
Primary Outcomes
Change in Oxford Knee Score Questionnaire
Time Frame: Baseline, Post-intervention (immediately after 6 month post-op intervention)
Subjectively measures functional ability. Minimum score: 0. Maximum score: 48. Higher score indicates better outcome.
Secondary Outcomes
- Change in EuroQol 5D3L Questionnaire(Baseline, Post-intervention (immediately after 6 month post-op intervention))
- Change in Pain Visual Analogue Scale(Baseline, Post-intervention (immediately after 6 month post-op intervention))
- Change in Keele Assessment of Participation Questionnaire(Baseline, Post-intervention (immediately after 6 month post-op intervention))
- Semi-structured interview(Post-intervention (immediately after 6 month post-op intervention))
- Change in Timed Up and Go Test(Baseline, Post-intervention (immediately after 6 month post-op intervention))
- Satisfaction Survey(Post-intervention (immediately after 6 month post-op intervention))
Investigators
Brodie Sakakibara
Assistant Professor
University of British Columbia