NCT05736133

Brief Summary

This is a pilot cluster randomized controlled trial to to evaluate the individual and health system impacts of implementing a new physiotherapist-led primary care model for hip and knee pain in Canada.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
205

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Oct 2023

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 9, 2023

Completed
12 days until next milestone

First Posted

Study publicly available on registry

February 21, 2023

Completed
7 months until next milestone

Study Start

First participant enrolled

October 2, 2023

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 17, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 17, 2025

Completed
Last Updated

March 20, 2025

Status Verified

March 1, 2025

Enrollment Period

1.3 years

First QC Date

February 9, 2023

Last Update Submit

March 17, 2025

Conditions

Outcome Measures

Primary Outcomes (4)

  • Participant Recruitment Rate

    A full trial will be feasible if the investigators are able to recruit 1.5 participants per week per site over 20 weeks

    20 weeks

  • Assessment Procedures

    The investigators consider ≥80% of all assessment items completed and a mean time for completion of ≤60 minutes acceptable.

    12 months

  • Retention

    The investigators consider an attrition rate of ≤20% at 12-month follow-up successful. ≤35% attrition will be considered partially successful; however, additional retention strategies would be required for the full trial based on evidence that ≥20% attrition threatens trial validity

    12 months

  • PT Treatment Fidelity

    Treatment fidelity will be measured through an audit of a PT fidelity checklist and electronic medical record (EMR) to determine the consistency of the care provided. An acceptable level of fidelity will be considered ≥80% for each intervention component.

    20 weeks

Secondary Outcomes (31)

  • Self-Reported Functioning

    Baseline and 3, 6, 9, and 12 months follow-up

  • Self-Reported Pain Intensity

    Baseline and 3, 6, 9, and 12 months follow-up

  • Health-Related Quality of Life

    Baseline and 3, 6, 9, and 12 months follow-up

  • Pain Self Efficacy

    Baseline and 3, 6, 9, and 12 months follow-up

  • Catastrophic Thinking

    Baseline and 3, 6, 9, and 12 months follow-up

  • +26 more secondary outcomes

Other Outcomes (4)

  • Baseline Characteristics

    Baseline

  • Comorbidities

    Baseline

  • Chronicity of Pain

    Baseline

  • +1 more other outcomes

Study Arms (2)

Physiotherapist-led primary care model for hip and knee pain

EXPERIMENTAL

The index intervention will incorporate a PT within the primary care team and make them available at the first point of contact for people with hip or knee pain. There will be 4 key components of this intervention: 1) Initial assessment and screening; 2) Brief individualized intervention at first visit; 3) Health services navigation; 4) Providing additional PT care for people with an unmet need (e.g., no insurance coverage for PT).

Other: Physiotherapist-led primary care model for hip and knee pain

Usual physician-led primary care model for hip and knee pain

ACTIVE COMPARATOR

Participants will be seen by a primary care physician or a nurse practitioner, depending on the current practice at the clinic. Participants in both groups will be permitted to seek additional care outside of the primary care clinic.

Other: Usual physician-led primary care model for hip and knee pain

Interventions

1. Initial assessment and screening: The PT will provide a comprehensive assessment according to established clinical practice guidelines. 2. Brief individualized intervention at first visit: The PT intervention will be at the discretion of the PT to reflect real-world PT intervention. 3. Health services navigation: Participants will be provided with options available to them in their community for rehabilitation. For example, they may be referred to community PT for ongoing management or presented with group exercise options. Participants will be assessed regarding the need for specialist referrals or resources available to manage complex clinical presentations such as comorbidity or frailty. Participants may be referred to the primary care provider if no specialized services are needed or when the PT cannot provide a direct referral. All individuals may have their medications reviewed by a physician if deemed appropriate by the PT or requested by the participant.

Physiotherapist-led primary care model for hip and knee pain

The physician led primary care intervention will be unstandardized to best reflect standard clinical practice in Canada.

Usual physician-led primary care model for hip and knee pain

Eligibility Criteria

Age19 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • \- Adults \>= 19 years who ask to book a primary care visits where the primary reason is for hip or knee pain of any duration.

You may not qualify if:

  • Cannot understand, read, and write English
  • Known cancer causing hip or knee pain

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Queen's University

Kingston, Ontario, K7L 3N6, Canada

Location

MeSH Terms

Conditions

Osteoarthritis, HipOsteoarthritis, Knee

Interventions

Papaverine

Condition Hierarchy (Ancestors)

OsteoarthritisArthritisJoint DiseasesMusculoskeletal DiseasesRheumatic Diseases

Intervention Hierarchy (Ancestors)

BenzylisoquinolinesAlkaloidsHeterocyclic CompoundsOpiate AlkaloidsIsoquinolinesHeterocyclic Compounds, 2-RingHeterocyclic Compounds, Fused-Ring

Study Officials

  • Jordan Miller, PhD

    Queen's University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Masking Details
Due to the nature of the new model of care and comparison, it is not possible to blind the patient participants or health care providers. Since the primary outcomes are self-reported outcome measures, the assessor is also not blind to the intervention.
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: This is a pilot cluster randomized controlled trial randomizing 14 sites to the PT-led primary care model for hip/knee pain or to the usual care model
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Assistant Professor, School of Rehabilitation Therapy, Queen's University

Study Record Dates

First Submitted

February 9, 2023

First Posted

February 21, 2023

Study Start

October 2, 2023

Primary Completion

January 17, 2025

Study Completion

January 17, 2025

Last Updated

March 20, 2025

Record last verified: 2025-03

Data Sharing

IPD Sharing
Will not share

The is no plan to share individual IPD with other researchers

Locations