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Evaluation of a Community Pharmacist Managed Asthma Consultation Service

2018年8月27日 更新者:Zahava Rosenberg-Yunger

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.

調査の概要

研究の種類

介入

入学 (実際)

19

段階

  • 適用できない

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

はい

受講資格のある性別

全て

説明

Inclusion Criteria:

  • Provided written consent
  • Intending to refill all asthma-related prescriptions at the study pharmacy
  • Diagnosed with asthma by a physician or nurse practitioner
  • Taking inhaled corticosteroids for which the dose and/or medication has remained unchanged for at least 2 months
  • 18 years of age or older
  • Uncontrolled asthma (defined as in the past 4 weeks the patient has used their rescue medications 4 or more times in a given week and/or the patient has woken up in the night from their asthma in a given week).

Exclusion Criteria:

  • Pregnant women
  • Unable or unwilling to return to the pharmacy for scheduled visits
  • Unable to speak English language well enough to communicate with the pharmacist and complete the questionnaires independently
  • Terminal illness or poor prognosis (life expectancy less than 3 years)
  • History of alcoholism or drug abuse
  • Comorbidities/health issues:

    • Chronic obstructive pulmonary disorder (emphysema; chronic bronchitis)
    • Acute respiratory infection
    • Pulmonary fibrosis
    • Cancer (in the past 5 years preceding enrolment)
    • Organ transplantation
    • Dementia, cognitive impairment or other psychiatric disorder (Cognitive Impairments such as those found under the Diagnostic and Statistical Manual of Mental Disorders (DSM-IV-TR) common Axis I and Axis II disorders
    • Any other health issue that may hinder performance on pulmonary function test
  • Enrolled in an Employee Assistance Program for disease management within 6 months preceding the study enrolment date OR planning to enroll in the next 12 months
  • Enrolled in another asthma management/clinical study OR planning to enroll in a similar study in the next 12 months
  • Had a MedsCheck or MedsCheck Follow-Up done within the 3-month period preceding the anticipated date of the first study appointment
  • Patients who do not wish their physician to be notified of their participation

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:ヘルスサービス研究
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
アクティブコンパレータ:Control Group
Patients in the control group will receive standard, dispensing services they currently receive from pharmacists. Control group pharmacists will continue to provide these services in accordance with the standards of practice adopted by the Ontario College of Pharmacists. They will not provide either of the 3 intervention components outlined above. Should a control group patient request additional information and/or services, the pharmacist will comply and provide these as deemed necessary for the particular patient. This could include the full range of educational and drug therapy optimization services outlined for the intervention group. If this occurs then the pharmacists will document all services provided in order for the research team to account for this in the analysis.
実験的:Intervention Group

Pharmacists in the intervention group will provide patients with a comprehensive disease management program for asthma. The 3 major components of pharmacists' intervention are outlined below. The services delivered will be customized based on each patient's case.

  1. Medication review and drug therapy optimization
  2. Patient education
  3. Improving patient adherence
他の名前:
  • Pharmacist Asthma Intervention

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Peak Expiratory Flow Rate (PEF)
時間枠:Pharmacist will measure peak flow rate incrementally each month for 12 months total.
A peak flow meter will be used to measure PEF.
Pharmacist will measure peak flow rate incrementally each month for 12 months total.

二次結果の測定

結果測定
メジャーの説明
時間枠
Peak Flow Diary
時間枠: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.
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.
Asthma Control
時間枠: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.
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 Medication Adherence Report Scale for Asthma
時間枠: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.
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).
Health Care Service Usage Questionnaire
時間枠: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.
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).
Asthma Quality of Life Questionnaire (AQLQ)
時間枠: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.
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).
Heath and Work Performance Questionnaire
時間枠: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.
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).
Asthma Self-Management Questionnaire
時間枠: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.
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).
Asthma General Knowledge Questionnaire for Adults
時間枠: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.
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).
Patient Satisfaction Questionnaire
時間枠: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.
The pharmacist will distribute this questionnaire to patients at the final appointment (12 months after baseline).

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • 主任研究者:Zahava Rosenberg-Yunger, PhD、Ryerson University; Ontario Pharmacists Association

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2016年6月1日

一次修了 (実際)

2018年4月16日

研究の完了 (実際)

2018年4月16日

試験登録日

最初に提出

2016年3月8日

QC基準を満たした最初の提出物

2016年5月9日

最初の投稿 (見積もり)

2016年5月11日

学習記録の更新

投稿された最後の更新 (実際)

2018年8月28日

QC基準を満たした最後の更新が送信されました

2018年8月27日

最終確認日

2018年8月1日

詳しくは

本研究に関する用語

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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