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PharmacyeAMS-PharmNCT07038642

The Electronic Asthma Management System in Pharmacies

A study testing Pharmacy Clinical Decision Support System for Asthma Management in people with Pharmacy and Asthma Management, run by Unity Health Toronto at 3 sites in Canada.

Enrolling by invitation

Enrolling by invitation. The study team selects and invites participants, usually from an existing group of patients.

Sites and contacts
Official record
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Trial summary

The goal of this study is to assess the effect of an electronic asthma management system in pharmacies (eAMS-Pharm) on asthma control assessment, asthma medication adjustment, asthma action plan delivery, and prompting for specialist referral in severe asthma. Read more about this study

Who is it for?
Ages 16 years and older
Conditions the study is for
Pharmacy, Asthma Management, Asthma
What is being tested?
Pharmacy Clinical Decision Support System for Asthma Management
Could I receive a placebo?
No, everyone receives an active treatment
How many people
100 participants
Where
3 sitesCanada
Study dates
23 Jun 2025to 15 Jan 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 16 years and older
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult
  • Eligible patients would be those who have asthma and are seen at one of the three study pharmacies during the study period
  • Eligible pharmacy team members would be staff (pharmacists/RPhTs/assistants/students) at any one of the three study pharmacies

Trial locations and contacts

3 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Canada3 sites
  • Medical Place Pharmacy

    Ajax, Ontario, L1L 2J5

  • LiveWell Pharmacy

    Niagara Falls, Ontario, L2J 2K5

  • Westmount Place Pharmacy

    Waterloo, Ontario, N2L 2R5

Other trials in Canada

About this study

Official title: The Electronic Asthma Management System in Pharmacies (eAMS-Pharm)

The goal of this study is to assess the effect of an electronic asthma management system in pharmacies (eAMS-Pharm) on asthma control assessment, asthma medication adjustment, asthma action plan delivery, and prompting for specialist referral in severe asthma. The study assesses the differences on pharmacy processes (affecting both the pharmacy team and patients) and pharmacy-delivered care using an interrupted time-series analysis (six-months before vs. six-months after the introduction of eAMS-Pharm in study pharmacy sites).

The eAMS-Pharm uses patient data (asthma control, asthma flare-up risk, and current medications) to provide clinical decision support to pharmacists, empowering them to bridge existing gaps between guideline-recommended asthma care and patient care received.

Read the detailed description

Asthma is the third most common chronic disease in adults and is increasing in prevalence. Although effective therapies exist and well-controlled asthma is achievable in most patients, studies demonstrate that up to 90% of Canadians with asthma are poorly controlled. This poor control and associated health system burden are attributable to 4 major gaps in care: 1) failure to ascertain asthma control according to guideline criteria; 2) failure to escalate pharmacotherapy in response to suboptimal control; 3) failure to provide a written asthma action plan (AAP) (a personalized plan produced by a health care professional for a patient, providing education and guidance for self-management of flares); and 4) failure to refer patients with severe asthma to specialty care for biologic therapies (these were 4 of the 6 quality statements in Health Quality Ontario's Asthma Quality Standards).

The Electronic Asthma Management System (eAMS) is a validated tool that has the potential to address the 4 major gaps in care. The eAMS consists of a web-based portal-based e-questionnaire, which collects asthma parameters directly from patients. A point-of-care Computerized Decision Support System (CDSS) receives and processes questionnaire data to produce guideline-based decision support such as assessments of asthma control, relevant medication change recommendations, and a personalized asthma action plan (AAP). There are also web-based education resources in the patient portal. The eAMS was proven to improve asthma management in primary care across these care gaps and is used in 16 primary care clinics, with ~215 providers and ~7200 patients with asthma. Now, with the increasingly critical role that pharmacists are playing in Canada's healthcare ecosystem, the eAMS can also be used to empower pharmacists to help optimize chronic disease care.

Pharmacists' scope of practice is growing rapidly in Ontario and across Canada. At the same time, asthma control remains suboptimal for millions of Canadians. Furthermore, the eAMS has been extensively studied and validated as an optimal tool to improve asthma management in primary care. The use of the eAMS in pharmacies presents a unique opportunity to involve pharmacists in chronic disease care while also reducing the burden on primary care. To address limited primary care access and given rapid the expansion of pharmacists' role of in care delivery, the investigators adapted the platform to build the eAMS-Pharm - a chronic disease quality improvement tool for pharmacists. The results of this study will inform the broader implementation of the eAMS across pharmacies and similar knowledge translation tools in pharmacies in the future.

Being tested
Pharmacy Clinical Decision Support System for Asthma Management
Keywords
Asthma, Pharmacy, Asthma management, Computerized decision support system
Medical subject headings
Asthma

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Pharmacy Clinical Decision Support System for Asthma ManagementBehavioural

    A pharmacy clinical decision support system that generates individualized advice for asthma patients is provided to the pharmacist/RPht/assistant/student.

Study groups in NCT07038642
Study groupRoleWhat they receive
Control - NoneNo interventionA retrospective, pharmacy chart review will assess pharmacy-delivered care in the six-month pre-intervention period.
Intervention - The Electronic Asthma Management System in Pharmacies (eAMS-Pharm)Active comparatorThroughout the intervention period, the eAMS-Pharm will be provided to pharmacists/RPhTs/assistants/students (for use in eligible patients).
Receives: Behavioral: Pharmacy Clinical Decision Support System for Asthma Management

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Medication adjustments

    Using pharmacist chart review, the investigators will assess the proportion and trend in patients receiving medication adjustments

    Measured: 12 months, broken into individual time series periods

  2. Asthma control assessment

    Using pharmacist chart review, the investigators will assess the proportion and trend of patients receiving asthma control assessment by guideline criteria

    Measured: 12 months, broken into individual time series periods

  3. Asthma action plan creation

    Using pharmacist chart review, the investigators will assess the proportion and trend of asthma action plans being created for patients

    Measured: 12 months, broken into individual time series periods

Secondary outcomes (15)
  1. System usage: virtual and in-person visit frequency

    Using pharmacist chart review, investigators will assess the number of times the system was used in virtual (i.e., telemedicine) visits and in in-person visits

    Measured: 6 months

  2. System usage: content access frequency

    Using system analytics, investigators will assess the type of content accessed (clinical tools, clinical decisions, educational materials) by patients and pharmacy teams

    Measured: 6 months

  3. System usage: patient engagement frequency, by method

    Using system analytics, investigators will assess the number of patients who engaged with the system by the programmatic (mass invite) method, or as a walk-in patient following programmatic invitations

    Measured: 6 months

  4. System usage: time required for access and documentation

    Using system analytics, investigators will assess how long it takes pharmacy teams to access and complete clinical decision making within the system. Last screen timestamp minus first screen timestamp will be used to measure time

    Measured: 6 months

  5. Quantitative patient Likert-Scale questionnaire

    Exclusively throughout the intervention, electronic questionnaires developed by the investigators will be sent to consenting patients to assess quantitative patient feedback on system functionality and care quality received, as 5-point Likert scales. Multiple choice and yes/no questions will also bee used to determine demographics and relevant asthma diagnosis information

    Measured: 6 months

  6. Qualitative patient free-text feedback questionnaire

    Exclusively throughout the intervention, electronic questionnaires developed by the investigators will be sent to consenting patients to assess qualitative patient feedback on benefits and drawbacks of the system, as measured through two free-text questions

    Measured: 6 months

  7. Pharmacy team feedback: 10-item System Usability Scale - SUS

    Exclusively throughout the intervention, electronic questionnaires developed by the investigators will be sent to consenting pharmacy team members to assess feedback on system usability, as measured by The System Usability Scale (SUS), a 10-item 5-point Likert scale

    Measured: 6 months

  8. Quantitative pharmacy Likert-Scale questionnaire

    Exclusively throughout the intervention, electronic questionnaires developed by the investigators will be sent to consenting pharmacy team members to assess quantitative pharmacy team feedback on technology interest, role of pharmacies in chronic disease care and asthma action plans, system functionality, and benefits and drawbacks of the system on pharmacy workflows, as measured with 5-point Likert scales

    Measured: 6 months

  9. Qualitative pharmacy free-text feedback questionnaire

    Exclusively throughout the intervention, electronic questionnaires developed by the investigators will be sent to consenting pharmacy team members to assess qualitative pharmacy team feedback on system usage, as measured through 6 free text questions. To supplement the outcome of revenue metrics, the pharmacy team feedback questionnaire will also ask pharmacy team members to estimate revenue for time spent

    Measured: 6 months

  10. Prescription/action plan sign-back proportions

    Using pharmacist chart review, the investigators will assess the proportion of prescriptions/action plans which receive sign-back from prescribers in each analysis period

    Measured: 12 months, broken into individual time series periods

  11. Revenue metrics: pharmaceutical opinion proportion

    Using pharmacist chart review, the investigators will assess the proportion of eligible visits for which a pharmaceutical opinion was successfully billed

    Measured: 12 months, broken into individual time series periods

  12. Revenue metrics: MedsCheck proportion

    Using pharmacist chart review, the investigators will assess the proportion of eligible visits for which a MedsCheck was successfully billed

    Measured: 12 months, broken into individual time series periods

  13. Revenue metrics: total dollar revenue per patient

    Using pharmacist chart review, the investigators will assess the total average revenue per eligible patient by summing pharmaceutical opinion, MedsChecks, markups, and dispensing fees

    Measured: 12 months, broken into individual time series periods

  14. Revenue metrics: dollar reimbursement for time spent in system

    Using pharmacist chart review, the investigators will assess the overall reimbursement for time pharmacy team members spent in the system. To measure, investigators will sum the total revenue per patient and divide by time spent in the system for each patient over visits. An average will be calculated across all patients

    Measured: 6 months

  15. Specialist referral prompt proportion

    Using pharmacist chart review, the investigators will assess the proportion of severe asthma patients, as identified by medications currently prescribed and filled, and who are not already seeing a specialist, for whom a prompt for specialist referral was sent to the prescriber

    Measured: 12 months, broken into individual time series periods

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Jun 2025
  2. Study start23 Jun 2025
  3. Primary completion23 Dec 2025 (estimated)
  4. Study completion15 Jan 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Health services research
Allocation
Non-randomised
Intervention model
Sequential
Model description
Interrupted time series analysis
Masking
None (open label)
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07038642
Sponsor's protocol ID
46441
Acronym
eAMS-Pharm
Status last verified
Aug 2025
First submitted
5 Jun 2025
Last updated
17 Aug 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Pharmacy Clinical Decision Support System for Asthma Management in people with Pharmacy and Asthma Management, run by Unity Health Toronto at 3 sites in Canada.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: enrolling by invitation, as of the sponsor's last update on 17 Aug 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 3 sites in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Medication adjustments (time frame: 12 months, broken into individual time series periods). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Aug 2025.

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