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Determining the Impact of a New Physiotherapist Led Primary Care Model for Back Pain

Primary Purpose

Back Pain

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Physiotherapist-led primary care model for back pain
Usual care
Sponsored by
Queen's University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Back Pain

Eligibility Criteria

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

Inclusion Criteria:

  • Adults (18 years and over) with back pain of any duration
  • Seeking primary care for back pain at a participating site
  • Primary care visit may be a first or repeat visit

Exclusion Criteria:

  • Patients who do not consent to participation
  • Patients who report being unable to understand, read, and write English

Sites / Locations

  • Queen's University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Physiotherapist-led primary care model for back pain

Usual care

Arm Description

The PT-led primary care model for back pain will involve incorporating a PT within the primary care team at the first point of contact for people with back pain at no cost to the patient. Patients in this model will be given the choice of seeing the PT or family doctor. They will be encouraged to book with the PT except when the primary reason for visit is for medication renewals or when the patient has additional health concerns that need attention from their physician in the same visit. There will be 4 key components of the PT led primary care intervention: 1) Initial assessment and screening; 2) Brief individualized intervention at the first visit; 3) Health services navigation; 4) Providing additional PT care for people with an unmet need.

The physician led primary care intervention will be unstandardized to best reflect standard clinical practice in Canada. This usually includes a visit to a primary care physician, who would perform a history and physical examination, provide LBP education, and prescribe medications and/or refer based on their assessment findings and patient preferences.

Outcomes

Primary Outcome Measures

Recruitment of primary care teams
Ability to recruit four primary care teams (Family Health Teams or Community Health Centres) to paricipate
Recruitment of patient participants
Recruitment rate (participants/week) or total number of participants recruited in 14 weeks
Assessment completion
Percentage of all assessment items completed by participants completing each assessment
Retention of patient participants
Attrition rate
Physiotherapist confidence in carrying out the interventions
The PT will rate his/her confidence in each component of the intervention after the training on a scale from 0-10 with higher scores indicating greater confidence in carrying out that component of the intervention.
Treatment fidelity
Treatment fidelity will be measured by consistency with the intervention described in the protocol measured through an intervention checklist completed by the physiotherapist and an audit of the EMR notes.

Secondary Outcome Measures

Self-reported disability
measured using the Roland Morris Disability Questionnaire (0 to 24 with higher scores indicating greater disability)
Self-reported pain intensity
measured using a numeric pain rating scale from 0 to 10 with higher scores indicating greater pain intensity (measured at rest, during walking, and during a lifting task)
Health Related Quality of Life
measured using the EuroQoL-5D-5L (0 to 100 with greater scores indicating greater self-reported health related quality of life)
Global rating of change
measured using an 11-point scale (-5 to +5 with negative scores indicating a worsening of physical functioning related to back pain and positive scores indicating an improvement of physical functioning related to back pain)
Satisfaction with health care
measured using an 11-point scale(-5 to +5 with negative scores indicating a dissatisfaction with health care received and positive scores indicating satisfaction with health care received)
Catastrophic Thinking
measured using the Pain Catastrophizing Scale (0 to 52 with higher scores indicating greater catastrophic thinking)
Depressive symptoms
measured using the 9-item Patient Health Questionnaire (PHQ-9) (0 to 27 with greater scores indicating increased depressive symptoms)
Adverse events
measured using an adverse events questionnaire that asks 1) if the patient has experienced any adverse events as a result of the treatments received (yes/no); 2) how long the event lasted (hours or days); 3) how severe the adverse event was (0-10 scale); 4) what adverse events were experienced.
Health care accessibility
Percentage of patients receiving care within 48 hours.
Health care accessibility
Percentage of patients who score medium or high risk on the STarT Back tool who receive physiotherapy care.
Health care utilization
All health care visits (aggregated and dis-aggregated) including: primary care visits, emergency department visits, hospitalizations, surgeries, consultations with other health care providers, diagnostic imaging, medications, and other care received by the patient
Costs (piloted for a cost utility analysis in a future trial)
Includes all health care costs plus societal costs using a human capital approach for loss of productivity
Medications prescribed
Measured as a process outcome
Diagnostic imaging ordered
Measured as a process outcome
referrals to other health care providers made
Measured as a process outcome
notes made by primary care provider to employers or insurers
Measured as a process outcome

Full Information

First Posted
October 16, 2017
Last Updated
March 21, 2019
Sponsor
Queen's University
Collaborators
Canadian Institutes of Health Research (CIHR)
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1. Study Identification

Unique Protocol Identification Number
NCT03320148
Brief Title
Determining the Impact of a New Physiotherapist Led Primary Care Model for Back Pain
Official Title
Determining the Impact of a New Physiotherapist Led Primary Care Model for Back Pain: A Pilot Cluster Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2019
Overall Recruitment Status
Completed
Study Start Date
September 20, 2017 (Actual)
Primary Completion Date
January 15, 2019 (Actual)
Study Completion Date
January 15, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Queen's University
Collaborators
Canadian Institutes of Health Research (CIHR)

4. Oversight

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

5. Study Description

Brief Summary
This is a pilot cluster randomized controlled trial to determine the feasibility of a cluster randomized trial to evaluate the individual and health system impact of implementing a new physiotherapist-led primary care model for back pain in Canada.
Detailed Description
This study aims to determine the feasibility of conducting a cluster randomized trial in primary care settings in Ontario to evaluate the individual health outcomes and health system impact of implementing a new physiotherapist-led primary care model for people with back pain. The primary purpose of this pilot study is to determine the feasibility including recruitment and retention of primary care teams (sites) and patient participants, carrying out the assessment procedures, and implementing the physiotherapist-led primary care intervention including training the physiotherapist to adopt this role.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Back Pain

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
This is a pilot cluster randomized controlled trial randomizing 4 sites to the PT-led primary care model for back pain or usual care model
Masking
None (Open Label)
Masking Description
Due to the nature of the new model of care and comparison, it is not possible to blind the patients or health care providers. Since the primary outcomes are self-reported outcome measures, the assessor is also not blind to the intervention.
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Physiotherapist-led primary care model for back pain
Arm Type
Experimental
Arm Description
The PT-led primary care model for back pain will involve incorporating a PT within the primary care team at the first point of contact for people with back pain at no cost to the patient. Patients in this model will be given the choice of seeing the PT or family doctor. They will be encouraged to book with the PT except when the primary reason for visit is for medication renewals or when the patient has additional health concerns that need attention from their physician in the same visit. There will be 4 key components of the PT led primary care intervention: 1) Initial assessment and screening; 2) Brief individualized intervention at the first visit; 3) Health services navigation; 4) Providing additional PT care for people with an unmet need.
Arm Title
Usual care
Arm Type
Active Comparator
Arm Description
The physician led primary care intervention will be unstandardized to best reflect standard clinical practice in Canada. This usually includes a visit to a primary care physician, who would perform a history and physical examination, provide LBP education, and prescribe medications and/or refer based on their assessment findings and patient preferences.
Intervention Type
Behavioral
Intervention Name(s)
Physiotherapist-led primary care model for back pain
Intervention Description
Assessment and screening: taking a history; screening for red flags, comorbidities, and risk factors of ongoing pain and disability; physical examination Brief individualized intervention at the first visit: effective communication, cognitive reassurance, a few exercises, and advice/strategies to stay active. Health services navigation: PT assistance with navigating healthcare services based on the assessment findings. First, red-flags requiring emergency or urgent referrals. Next, comorbid conditions that would benefit from care from other healthcare providers. Finally, referral to PT (if appropriate). Providing additional physiotherapy care to people with an unmet need: Additional physiotherapy care will be provided to patients who have an identified need for physiotherapy but no physiotherapy coverage through private or government health insurance plans.
Intervention Type
Other
Intervention Name(s)
Usual care
Intervention Description
The physician led primary care intervention will be unstandardized to best reflect standard clinical practice in Canada.
Primary Outcome Measure Information:
Title
Recruitment of primary care teams
Description
Ability to recruit four primary care teams (Family Health Teams or Community Health Centres) to paricipate
Time Frame
Baseline
Title
Recruitment of patient participants
Description
Recruitment rate (participants/week) or total number of participants recruited in 14 weeks
Time Frame
Baseline to 14 weeks
Title
Assessment completion
Description
Percentage of all assessment items completed by participants completing each assessment
Time Frame
Baseline, 6-week 12-week, 6,9,12 month follow-up. The primary time point for this assessment is 12-week follow-up.
Title
Retention of patient participants
Description
Attrition rate
Time Frame
Retention of participants at 6-week, 12-week, 6, 9, and 12-month follow-up assessments. The primary timeline for this outcome is 12-month follow-up.
Title
Physiotherapist confidence in carrying out the interventions
Description
The PT will rate his/her confidence in each component of the intervention after the training on a scale from 0-10 with higher scores indicating greater confidence in carrying out that component of the intervention.
Time Frame
Baseline
Title
Treatment fidelity
Description
Treatment fidelity will be measured by consistency with the intervention described in the protocol measured through an intervention checklist completed by the physiotherapist and an audit of the EMR notes.
Time Frame
6-week follow-up
Secondary Outcome Measure Information:
Title
Self-reported disability
Description
measured using the Roland Morris Disability Questionnaire (0 to 24 with higher scores indicating greater disability)
Time Frame
Baseline, 6-week, 12-week, 6-month, 9-month, and 12-month follow-up
Title
Self-reported pain intensity
Description
measured using a numeric pain rating scale from 0 to 10 with higher scores indicating greater pain intensity (measured at rest, during walking, and during a lifting task)
Time Frame
Baseline, 6-week, 12-week, 6-month, 9-month, and 12-month follow-up
Title
Health Related Quality of Life
Description
measured using the EuroQoL-5D-5L (0 to 100 with greater scores indicating greater self-reported health related quality of life)
Time Frame
Baseline, 6-week, 12-week, 6-month, 9-month, and 12-month follow-up
Title
Global rating of change
Description
measured using an 11-point scale (-5 to +5 with negative scores indicating a worsening of physical functioning related to back pain and positive scores indicating an improvement of physical functioning related to back pain)
Time Frame
Baseline, 6-week, 12-week, 6-month, 9-month, and 12-month follow-up
Title
Satisfaction with health care
Description
measured using an 11-point scale(-5 to +5 with negative scores indicating a dissatisfaction with health care received and positive scores indicating satisfaction with health care received)
Time Frame
Baseline, 6-week, 12-week, 6-month, 9-month, and 12-month follow-up
Title
Catastrophic Thinking
Description
measured using the Pain Catastrophizing Scale (0 to 52 with higher scores indicating greater catastrophic thinking)
Time Frame
Baseline, 6-week, 12-week, 6-month, 9-month, and 12-month follow-up
Title
Depressive symptoms
Description
measured using the 9-item Patient Health Questionnaire (PHQ-9) (0 to 27 with greater scores indicating increased depressive symptoms)
Time Frame
Baseline, 6-week, 12-week, 6-month, 9-month, and 12-month follow-up
Title
Adverse events
Description
measured using an adverse events questionnaire that asks 1) if the patient has experienced any adverse events as a result of the treatments received (yes/no); 2) how long the event lasted (hours or days); 3) how severe the adverse event was (0-10 scale); 4) what adverse events were experienced.
Time Frame
Baseline, 6-week, 12-week, 6-month, 9-month, and 12-month follow-up
Title
Health care accessibility
Description
Percentage of patients receiving care within 48 hours.
Time Frame
Baseline, 6-week, 12-week, 6-month, 9-month, and 12-month follow-up
Title
Health care accessibility
Description
Percentage of patients who score medium or high risk on the STarT Back tool who receive physiotherapy care.
Time Frame
Baseline, 6-week, 12-week, 6-month, 9-month, and 12-month follow-up
Title
Health care utilization
Description
All health care visits (aggregated and dis-aggregated) including: primary care visits, emergency department visits, hospitalizations, surgeries, consultations with other health care providers, diagnostic imaging, medications, and other care received by the patient
Time Frame
Baseline, 6-week, 12-week, 6-month, 9-month, and 12-month follow-up
Title
Costs (piloted for a cost utility analysis in a future trial)
Description
Includes all health care costs plus societal costs using a human capital approach for loss of productivity
Time Frame
Baseline, 6-week, 12-week, 6-month, 9-month, and 12-month follow-up
Title
Medications prescribed
Description
Measured as a process outcome
Time Frame
Baseline, 6-week, 12-week, 6-month, 9-month, and 12-month follow-up
Title
Diagnostic imaging ordered
Description
Measured as a process outcome
Time Frame
Baseline, 6-week, 12-week, 6-month, 9-month, and 12-month follow-up
Title
referrals to other health care providers made
Description
Measured as a process outcome
Time Frame
Baseline, 6-week, 12-week, 6-month, 9-month, and 12-month follow-up
Title
notes made by primary care provider to employers or insurers
Description
Measured as a process outcome
Time Frame
Baseline, 6-week, 12-week, 6-month, 9-month, and 12-month follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adults (18 years and over) with back pain of any duration Seeking primary care for back pain at a participating site Primary care visit may be a first or repeat visit Exclusion Criteria: Patients who do not consent to participation Patients who report being unable to understand, read, and write English
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jordan Miller, PhD
Organizational Affiliation
Queen's University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Queen's University
City
Kingston
State/Province
Ontario
ZIP/Postal Code
K7L 3N6
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
There is no plan to share individual participant data from this pilot study. This data will be used to inform the protocol for a fully powered cluster randomized trial.
Citations:
PubMed Identifier
29121989
Citation
Miller J, Barber D, Donnelly C, French S, Green M, Hill J, MacDermid J, Marsh J, Norman K, Richardson J, Taljaard M, Wideman T, Cooper L, McPhee C. Determining the impact of a new physiotherapist-led primary care model for back pain: protocol for a pilot cluster randomized controlled trial. Trials. 2017 Nov 9;18(1):526. doi: 10.1186/s13063-017-2279-7.
Results Reference
derived

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Determining the Impact of a New Physiotherapist Led Primary Care Model for Back Pain

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