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Impacts of an Advanced Practice Physiotherapy Model of Care for Adults With a Peripheral Musculoskeletal Disorders Referred to an Orthropaedic Outpatient Clinic

Impacts of an Advanced Practice Physiotherapy Model of Care for Adults With a Peripheral Musculoskeletal Disorders Referred to an Orthropaedic Outpatient Clinic: a Prospective Observational Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05714332
Enrollment
104
Registered
2023-02-06
Start date
2022-11-15
Completion date
2024-01-02
Last updated
2025-07-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Musculoskeletal Disorders

Keywords

Advanced practice, Physiotherapy, Musculoskeletal disorders, Orthopedic, Observation

Brief summary

The goal of this prospective observational study is to evaluate advanced practice physiotherapy and orthopedic surgeon care and clinical outcomes for new patients with a peripheral musculoskeletal disorders consulting at the orthopedic outpatient clinic of the Hôpital Jean-Talon. The main questions it aims to answer are: 1. To describe the models of care at the Hôpital Jean-Talon orthopedic outpatient clinic; 2. To assess change in pain, disability, quality of life and pain catastrophizing at 6, 12 and 26 weeks after the initial evaluation; 3. To assess interprofessional collaboration between the advanced practice physiotherapists and orthopedic surgeons; 4. To assess patient satisfaction with care; 5. To assess waiting time before an initial consultation. Researchers will compare patients cared in the advanced practice physiotherapy and orthopedic surgeon group and the orthopedic surgeon only group.

Interventions

OTHERAdvanced practice physiotherapy and orthopedic surgeon management

Management of their musculoskeletal condition by an advanced practice physiotherapist and an orthopedic surgeon.

OTHEROrthopedic surgeon management

Management of their musculoskeletal condition by an orthopedic surgeon.

Sponsors

Ciusss de L'Est de l'Île de Montréal
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Adults with peripheral musculoskeletal disorders * New consultation at the Hôpital Jean-Talon orthopedic outpatient clinic * Legally able to consent * Understand and speak French or English * Beneficiaries of the provincial universal health insurance coverage (RAMQ)

Exclusion criteria

* Patients directly referred from the emergency department (not considered as patients referred to the outpatient clinic).

Design outcomes

Primary

MeasureTime frameDescription
Brief pain inventory severity6 weeks (change from baseline)Pain questionnaire (0-10; higher score=worse)
Brief pain inventory inventory6 weeks (change from baseline)Pain interference (disability) questionnaire (0-10; higher score=worse)

Secondary

MeasureTime frameDescription
Knee injury and Osteoarthritis Outcomes Score (KOOS)6 weeks (change from baseline)Disability questionnaire for knee disorders (0-100; higher=better)
Foot and Ankle Ability Measure (FAAM)6 weeks (change from baseline)Disability questionnaire for ankle/foot disorders (0-100; higher=better)
EQ-5D-5L6 weeks (change from baseline)Health-related quality of life questionnaire (to be converted in QALYs 0-1; higher=better)
EQ-5D-VAS6 weeks (change from baseline)Health-related quality of life questionnaire (0-100; higher=better)
Pain Catastrophizing Scale (PCS)6 weeks (change from baseline)Health-related quality of life questionnaire (0-50; higher=worse)
Patient perceptions of team effectiveness (Patient-PTE)0 week (post initial consultation)Perceptions of team effectiveness questionnaire (24-144; higher=better)
Shortened Disability of the Arm, Shoulder and Hand (QuickDASH)6 weeks (change from baseline)Disability questionnaire for upper extremity disorders (0-100; higher=worse)
Modified MedRisk12 weeksPatient satisfaction questionnaire (0-100; higher=better)
Provider perceptions of team effectiveness (Prodiver-PTE)Through study completion (once)Perceptions of team effectiveness questionnaire (26-156; higher=better)
Waiting timePre-interventionWaiting time (time in days and minutes)
Adverse events12 weeksRate of adverse events
Treatment and compliance6 weeksTreatment received and % of treatment compliance
modified validated version of the 9-item visit-specific satisfaction questionnaire (VSQ-9)0 week (post initial consultation)Patient satisfaction questionnaire (0-100; higher=better)
Hip disability and Osteoarthritis Outcomes Score (HOOS)6 weeks (change from baseline)Disability questionnaire for hip disorders (0-100; higher=better)

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026