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Impacts of Physiotherapy Services in a Quebec Emergency Department

Impacts of Physiotherapy Services in a Quebec Emergency Department - Randomized Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04009369
Enrollment
78
Registered
2019-07-05
Start date
2018-09-10
Completion date
2019-06-27
Last updated
2020-10-28

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

Conditions

Musculoskeletal Diseases, Musculoskeletal Injury, Musculoskeletal Pain

Keywords

Health care access, Health services, Professional practices

Brief summary

Emergency departments (ED) in several countries integrated physiotherapists in order to reduce wait times for patients with musculoskeletal disorders (MSKD). These initiatives have indeed reduced wait times, length of stay, time waited before seeing a professional and the prescription of unnecessary consultations and diagnostic tests. In Canada, such initiatives are marginal and their effects have not been studied. The objectives of the project are to evaluate the effects of physiotherapy management of patients with MSKD in ED compared to usual practice on clinical course of patients, use of services and resources, and waiting time and length of stay in ED. The hypothesis is that patients presenting with a MSKD to the ED with direct access to a physiotherapist will have better clinical outcomes and that use of services, waiting time, and length of stay are going to be inferior to those of the EP group.

Detailed description

Background and rationale: Emergency departments (ED) in several countries integrated physiotherapists, which led, for patients with musculoskeletal disorders (MSKD), to a reduction in wait times, length of stay, time waited before seeing a professional and the prescription of unnecessary consultations and diagnostic tests. Furthermore, early access to physiotherapy is associated with a decrease in pain and psychological symptoms and decreased risks of developing persistent pain. In Canada, such initiatives are still marginal and their effects have not been studied. Objectives: Evaluate the effects of direct access physiotherapy management of patients with MSKD in the ED compared to the usual management by the emergency physician on clinical course of patients (pain, quality of life and disability) and use of services and resources at one and three months, and waiting time and length of stay in the ED. Methods: A randomized controlled trial is currently in progress at the Centre hospitalier de l'Université Laval (CHUL). Two groups of 50 participants each are recruited over a six months period: one group with direct access to a physiotherapist (PT) in the ED and one control group with the usual access care to the emergency physician. Data is extracted from the patients' medical record, administrative data from the ED, self-administered forms given to the patients during their ED stay and either electronic or phone follow-ups (1 and 3 months). Data will be analysed using descriptive (demographic and clinical profiles) and inferential statistics (repeated ANOVA between groups across time points and Student T tests for independent samples). Importance of potential findings for MSK health: ED overcrowding causes prolonged lengths of stay, increased rates of patient leaving without being seen, increased medical errors, increased mortality among ambulatory and non-ambulatory patients and decreased patient satisfaction. This project will measure the effects of integrating PTs into the ED in a Canadian hospital setting and help identify ways to improve the current services offered to patients with a MSKD presenting to the ED. Direct access to PT may improve musculoskeletal health outcomes and support positive patient experience.

Interventions

OTHERDirect access to a PT

Direct access to a PT in the ED immediately after triage and prior to physician assessment.

Sponsors

CHU de Quebec-Universite Laval
CollaboratorOTHER
Integrated University Health and Social Services Center of the Capitale-Nationale
CollaboratorOTHER
Laval University
CollaboratorOTHER
Rose Gagnon
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Triage category 3, 4 or 5 * Discharged home with a minor MSKD after ED care * Able to consent * Able to understand French and to complete the questionnaire either verbally or in writing

Exclusion criteria

* Major MSKD requiring urgent care * Presence of a red flag or an unstable clinical condition * Living in a long-term care facility

Design outcomes

Primary

MeasureTime frameDescription
Level of Pain: Numeric Pain Rating ScaleBaseline, 1 and 3 monthsScale ranging from 0 to 10 where 0 means no pain at all and 10 means the worst pain ever.
Pain Interference on Function: Brief Pain InventoryBaseline, 1 and 3 monthsList of 10 items (work, sleep, general activity, etc.) represented on a scale ranging from 0 to 10 where 0 means Does Not Interfere and 10 means Completely Interferes. Subscales are averaged and the resulting score is out of 10. A higher score means a higher interference of pain on function.

Secondary

MeasureTime frameDescription
Diagnostic Tests : Standardized FormBaseline, 1 and 3 monthsForm were every diagnostic test received by the patient was checked as a Yes or No answer. (X-ray, MRI, CT Scan, ultrasound, etc.)
Consultations with Another Health Professional : Standardized FormBaseline, 1 and 3 monthsForm were every consultation being prescribed to the patient was checked as a Yes or No answer.
Pain Catastrophizing: Pain Catastrophizing ScaleBaselineList of 13 items (thoughts and feelings about pain) represented on a scale ranging from 0 to 4 where 0 means Not at all and 4 means All the time. Subscales are summed and the resulting score is out of 52. A higher score means a higher tendency to catastrophise pain.
Wait TimeBaselineDifference between beginning of the intervention and time of arrival between groups during their ED visit
Length of StayBaselineDifference between departure time and time of arrival between groups during their ED visit
Satisfaction: Visit-Specific Satisfaction InstrumentBaselineList of 7 items (Answers to your questions, Technical skills of the healthcare provider, etc.) represented on a scale ranging from 1 to 5 where 1 means Excellent and 5 means Poor. Subscales are transformed in results out of 100 (1 = 100% and 5 = 0%), averaged and the resulting score is out of 100%. A higher score means higher satisfaction.
Interventions received by the participants : Standardized FormBaseline, 1 and 3 monthsForm were every intervention received by the patient was checked as a Yes or No answer. (Advice, medication, technical aids, referral to another health professional, etc.)

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 8, 2026