Simultaneous Physiotherapy and Orthopedic Surgeon Interdisciplinary Care (SPOSIC)
SPOSIC
1 other identifier
interventional
30
0 countries
N/A
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Feb 2023
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 1, 2022
CompletedFirst Posted
Study publicly available on registry
December 27, 2022
CompletedStudy Start
First participant enrolled
February 1, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2024
CompletedDecember 27, 2022
December 1, 2022
1.5 years
December 1, 2022
December 21, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in Oxford Knee Score Questionnaire
Subjectively measures functional ability. Minimum score: 0. Maximum score: 48. Higher score indicates better outcome.
Baseline, Post-intervention (immediately after 6 month post-op intervention)
Secondary Outcomes (6)
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)
Change in EuroQol 5D3L Questionnaire
Baseline, 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)
- +1 more secondary outcomes
Study Arms (1)
Receives interdisciplinary sessions
EXPERIMENTALInterdisciplinary care by a team that includes: orthopedic surgeon, physiotherapist, a patient navigator, and the patient
Interventions
Along with usual care, participants receive six interdisciplinary sessions at 2 months and 1 month pre-operatively and 2 weeks, 6 weeks, 3 months, and 6 months post-operatively attended by an orthopedic surgeon, a physiotherapist, a patient navigator, and the patient. The pre-operative interdisciplinary sessions will outline expectations, explore patients' questions and concerns, set expectations for the next interdisciplinary session, and ensure goal congruence between all members of the team. Along with usual care during the post-operative period, participants will receive interdisciplinary sessions that 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.
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- Are living in long-term care
- Have significant neurological conditions
- Are medically unstable
- Have medical condition(s) significantly impacting lower extremity function
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of British Columbialead
- Interior Healthcollaborator
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Brodie Sakakibara, PhD
The University of British Columbia
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
December 1, 2022
First Posted
December 27, 2022
Study Start
February 1, 2023
Primary Completion
August 1, 2024
Study Completion
August 1, 2024
Last Updated
December 27, 2022
Record last verified: 2022-12
Data Sharing
- IPD Sharing
- Will not share