Comparing care for low-acuity patients in different healthcare settings
The Right Care, for the Right Patient, at the Right Time, by the Right Provider: A Value-based Comparison of the Management of Ambulatory Patients With Acute Health Concerns in walk-in Clinics, Primary Care Physician Practices and Emergency Departments
This study is testing how well low-acuity patients with common health issues are cared for in emergency rooms, walk-in clinics, and primary care offices, comparing in-person visits to telemedicine.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 4000 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | CHU de Quebec-Universite Laval Academic / other |
| Locations | 7 sites (Kingston, Ontario and 6 other locations) |
| Trial ID | NCT05892666 on ClinicalTrials.gov |
What this trial studies
This observational study aims to evaluate the value of care received by ambulatory patients with acute health concerns in emergency departments, walk-in clinics, and primary care practices. It will compare in-person visits and telemedicine consultations, focusing on various common complaints such as sore throat, cough, and urinary issues. Patients will be recruited through a random sampling schedule, with follow-up phone calls to assess their experiences and outcomes. The study seeks to provide insights into the cost-effectiveness and quality of care across different healthcare settings.
Who should consider this trial
Good fit: Ideal candidates include ambulatory patients aged 18 and over presenting with specific acute health complaints in emergency departments, walk-in clinics, or primary care practices.
Not a fit: Patients who are transported by ambulance or those not covered by provincial health insurance may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could help optimize healthcare delivery for low-acuity patients, potentially reducing unnecessary emergency department visits.
How similar studies have performed: Other studies have shown varying success in comparing care models for low-acuity patients, but this specific approach focusing on telemedicine during the COVID-19 pandemic is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
We shall include patients: 1. aged 18 years and over; 2. seen in person or via telemedicine in an ED, a walk-in clinic, or the primary care practice where they are registered; 3. ambulatory during the entire visit or consultation; 4. with one of the following presenting complaints: 1. acute diarrheas, defined as at least one day (24h) reported with three or more loose or liquid stools in the last seven days; 2. Sore throat; 3. Nasal congestion; 4. Increased or purulent nasal discharge; 5. Earache or ear discharge; 6. Shortness of breath; 7. Cough; 8. Increased or purulent sputum; 9. Muscle aches; 10. Anosmia; 11. Dysgeusia; 12. Burning urine; 13. Urinary frequency and urgency; 14. Dysuria; 15. Limb traumatic injury; 16. Cervical, thoracic or lumbar back pain; 17. Fever. We shall exclude patients: 1. transported by ambulance; 2. not covered by the provincial health insurance plan; 3. having consulted for a similar problem in the previous 30 days since patients with refractory disease represent a population with different care needs.; 4. living in a long-term healthcare facility or incarcerated; 5. with cognitive impairment that prevents reliable answers to the research questions; 6. receiving palliative care.
Where this trial is running
Kingston, Ontario and 6 other locations
- Kingston Health Sciences Centre — Kingston, Ontario, Canada (Not_yet_recruiting)
- Queen's Family Health Team — Kingston, Ontario, Canada (Not_yet_recruiting)
- Ottawa Hospital — Ottawa, Ontario, Canada (Not_yet_recruiting)
- CISSS de Lanaudière — Joliette, Quebec, Canada (Not_yet_recruiting)
- CIUSSS-Nord de Montréal — Montreal, Quebec, Canada (Not_yet_recruiting)
- CIUSSS de la Capitale-Nationale — Québec, Canada (Not_yet_recruiting)
- Centre de recherche CHU de Québec - Université Laval — Québec, Canada (Recruiting)
Study contacts
- Principal investigator: Simon Berthelot, MD MSc FRCPC CCMF(MU) — CHU de Québec-Université Laval
- Study coordinator: Simon Berthelot, MD MSc FRCPC
- Email: simon.berthelot@crchudequebec.ulaval.ca
- Phone: 418 525-4444
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.