Pharmacist led Asthma Management
OtherOther names: Pharmacist Asthma Intervention
NCT Number: NCT02768623
Asthma is one of the most common chronic health conditions, affecting 900,000 Ontarians, 2.4 million Canadians and over 300 million people worldwide. Unlike most other chronic diseases, asthma affects a significant proportion of children - an estimated 21% in Ontario. Asthma is also the leading cause of hospitalization for children in Canada and is a significant cause of school and work absenteeism. Though asthma is generally considered a chronic disease, it can be fatal in some instances - in 2009, an estimated 91 Ontarians died of this condition. Effective management of asthma can prevent exacerbation and more severe negative health consequences. In fact, estimates show that over 80% of the asthma-related deaths could be prevented through proper education. However, evidence also shows that over 55% of patients with moderate to severe asthma do not have their asthma symptoms under control, despite regular doctor visits. Less than a third (31%) of asthma patients report receiving an asthma action plan from their physicians, although such plans are associated with fewer ER visits, lower hospitalization rates and improved lung function. Hence, there is a clear opportunity to improve the management of asthma and reduce the incidence of related complications.
Given the scientific evidence of pharmacists effect on asthma management there is a strong rationale for introducing an asthma-specific pharmacist-led intervention for Ontarians suffering from this chronic disease. However, the implementation of such a program should be preceded by a pilot test to ensure that the program parameters are optimized to drive improved patient outcomes and maximum quality of service. The primary goals of this research project are to examine the impact of a pharmacist led asthma management intervention on patient health outcomes and to determine the optimum program structure to ensure quality of service delivery.
This study employs a mixed-methods study design. Investigators will begin with a cluster randomized controlled trial and end with exit interviews.This study will consist of a prospective, randomized controlled trial conducted in the community setting. A total of 12 pharmacies across the Greater Toronto Region will be recruited for this study. Each of these pharmacies will be randomly assigned in a 1:1 ratio to either the intervention group or the control group. All data will be analyzed using statistical software. Significance level will be set at 0.05. Pharmacy level descriptive characteristics, including mean and standard deviation for the number of patients will be reported. There is a low perceived risk for this study; however, the investigators will take every precaution to ensure this study is conducted in an ethical manner, including protecting patient confidentiality and anonymity.
Looking for future studies?
Notify Me18 year and older
All sexes
Interventional
Not applicable
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Other names: Pharmacist Asthma Intervention
Time frame: Pharmacist will measure peak flow rate incrementally each month for 12 months total.
A peak flow meter will be used to measure PEF.
Time frame: Patients will measure their peak flow twice daily (morning and night) throughout the duration of the study (i.e., 12 months) with their peak flow meter. They will document their peak flow measurements in a diary.
The peak flow diary is a chart given to patients to assist in recording their peak flow measurement using the peak flow meter.
Time frame: Pharmacist will measure Asthma control twice throughout duration of study. First, it will be measured at baseline (month 1) and lastly it will be measured at the final appointment (12 months after baseline).
The Asthma Control Questionnaire will be used to measure Asthma Control.
Time frame: Pharmacist will measure Medication Adherence twice throughout duration of study. First, it will be measured at baseline (month 1) and lastly it will be measured at the final appointment (12 months after baseline).
The Medication Adherence Report Scale for Asthma will be used to measure adherence to asthma medication.
Time frame: Pharmacist will measure Health Care Service Usage twice throughout duration of study. First, it will be measured at baseline (month 1) and lastly it will be measured at the final appointment (12 months after baseline).
The Health Care Service Usage Questionnaire will be used to measure a patient's utilization of health care services.
Time frame: Pharmacist will measure Asthma related quality of life twice throughout duration of study. First, it will be measured at baseline (month 1) and lastly it will be measured at the final appointment (12 months after baseline).
The AQLQ will be used to measure patient's quality of life.
Time frame: Pharmacist will measure health and work performance twice throughout duration of study. First, it will be measured at baseline (month 1) and lastly it will be measured at the final appointment (12 months after baseline).
The Heath and Work Performance Questionnaire will be used to measure patient's presenteeism and absenteeism due to asthma.
Time frame: Pharmacist will measure Asthma self-management twice throughout duration of study. First, it will be measured at baseline (month 1) and lastly it will be measured at the final appointment (12 months after baseline).
The Asthma Self-Management Questionnaire will be used to assess the patient's asthma management techniques.
Time frame: Pharmacist will measure Asthma general knowledge twice throughout duration of study. First, it will be measured at baseline (month 1) and lastly it will be measured at the final appointment (12 months after baseline).
The Asthma General Knowledge Questionnaire for Adult will be used to assess patient's asthma knowledge.
Time frame: The pharmacist will distribute this questionnaire to patients at the final appointment (12 months after baseline).
The Patient Satisfaction Questionnaire will be used to assess patients' satisfaction with the services they received over the study duration.
Zahava Rosenberg-Yunger
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT03978936
Asthma, Bronchial Diseases
Birmingham, Alabama, United States
View Trial DetailsNCT06448585
Allergic Rhinoconjunctivitis, Controlled Asthma
Don Benito, Badajoz, Spain
View Trial DetailsNCT02906761
Asthma, Bronchial Diseases
Besançon, France
View Trial DetailsNCT04865575
Pediatric Asthma, Uncontrolled Asthma
Regensburg, Germany
View Trial Details