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Набор скоро начнётся NCT07018583

Pharmacist Counseling & Self-Management Program for Asthma Patients in a Midwest Chain Pharmacy, USA

Без фазы С лечением Asthma Patients

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Pharmacist's Counseling and Self-Management Application Program, Usual Care.
Кому может быть актуально
Состояния в реестре: Asthma Patients. Базовые параметры: 25 лет — 64 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Список центров уточняется — проверьте первичный протокол.
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

The Effectiveness of Pharmacist's Counseling and Self-Management Application Program on Asthma Management Outcomes Among Asthma Patients at a Midwest Chain Pharmacy in Iowa, United States

Обзор

This clinical trial aims to evaluate the effectiveness of a pharmacist-led counseling and self-management application program on improving asthma management outcomes among adult patients with asthma receiving care at a Midwest chain pharmacy in Iowa, United States. The study investigates whether integrating the pharmacist counseling with self-management theory can enhance patients' medication adherence, asthma control, inhaler technique, and overall asthma awareness. These outcomes will be assessed at both 3 and 6 months after enrollment. Participants will be randomly assigned to one of two arms. The intervention group, which will receive a comprehensive pharmacist-led counseling program supported by a mobile application ("Don R.Ph Application"). The control group, which will receive standard pharmacy care as per usual practice.

Подробное описание

Protocol of the Study This research employs a randomized controlled trial (RCT) methodology to evaluate the effectiveness of a pharmacist-led counseling and self-management application program for asthma management.

Study Design:

This is a 6-month, repeated-measures, parallel-group RCT designed to assess the intervention's impact on asthma outcomes. The study comprises two groups:

Intervention Group: Participants will receive a pharmacist-led counseling session combined with access to a self-management mobile application.

Control Group: Participants will receive usual care provided within the pharmacy setting.

Data Collection Process:

1. Screening: Eligible participants will be identified based on predefined inclusion and exclusion criteria. 2. Randomization and Blinding: After screening, eligible participants will be randomly assigned to either the intervention or control group in a single-blind manner.

Sample Size and Allocation:

* A total of 397 patients with asthma diagnosis codes will be initially screened for eligibility. * Among these, 220 patients meeting the criteria will be assigned unique codes and recorded in Microsoft Excel.

Using simple randomization, 42 participants will be allocated to each group, maintaining a 1:1 ratio via computerized random number generation (using the RANDBETWEEN function in Excel) to minimize selection bias.

4\. Informed Consent: Participants will be provided with detailed study information and will give written informed consent prior to participation.

5\. Baseline Data Collection: Baseline demographic and clinical data will be gathered for all participants in both groups.

6\. Interventions:

* Intervention Group: Participants will undergo a structured pharmacist-led counseling and self-management program utilizing the "Don R.Ph. Asthma Management Application," a digital tool designed to support and monitor asthma management through six core steps over two 3-month cycles. * Control Group: Participants will receive standard pharmacy care, including medication reviews, patient education, and counseling on medication use as needed or upon request.

7\. Follow-up and Duration: Follow-up data will be collected at three and six months during and after the intervention period.

The study spans six months, with the intervention structured into six steps:

Month 1:

Step 1: Initial Disclosure Step 2: Problem Assessment Step 3: Commitment to Action Step 4: Skill Enhancement

Month 2:

Step 5: Monitoring via mobile application

Month 3:

Step 6: Follow-up and evaluation via mobile app and in-person counseling

This cycle will be repeated in months 4-6 to reinforce behavioral changes and optimize long-term outcomes.

The "Don R.Ph. Asthma Management Application" is a digital platform to support and monitor the pharmacist-led counseling process through eight key features:

1. Setting Your Goal! - Enables patients to establish personalized asthma management objectives. 2. Understanding Asthma - Offers educational videos about asthma and proper medication use. 3. How to Use Inhalers - Demonstrates correct inhaler techniques via videos. 4. Healthy Lifestyle - Shares practical tips to promote overall health and asthma control. 5. Asthma Self-Management \& Action Plan - Guides patients in creating and following tailored action plans. 6. Automated Consultation - Provides automated, personalized guidance and reminders 7. Let Us Know - Offers quick access to emergency pharmacist contact for urgent concerns. 8. Assess Your Goal Achievement - Allows patients to monitor their progress toward management goals through self-assessment tools.

Вмешательства

  • Поведенческое Pharmacist's Counseling and Self-Management Application Program
    This interventional study is structured around established counseling principles and self-management theory, consisting of six sequential stages: Initial Disclosure, Problem Assessment, Commitment to Action, Skill Enhancement, Monitoring, and Follow-up and Evaluation. These stages are delivered through both in-person pharmacist counseling and a dedicated mobile application. The intervention follows a repeated-measures design, with assessments conducted at 3 and 6 months after enrollment.
  • Поведенческое Usual Care
    Usual care or Standard pharmacy practices such as medication reviews, patient education during the initial visit or when medication changes occur, and counseling upon patient request. No additional structured counseling or self-management tools are provided.

Первичные конечные точки

  • Medication Adherence [Срок оценки: Baseline, 3 months, and 6 months]
  • Asthma Control [Срок оценки: Baseline, 3 months, and 6 months]
Вторичные конечные точки (2)
  • Inhaler technique skill [Срок оценки: Baseline, 3 months, and 6 months]
  • Asthma Awareness [Срок оценки: Baseline, 3 months, 6 months]

Критерии участия

Критерии включения

  • Adult patients with asthma are 25 - 64 years of age.
  • Have been receiving medications from the pharmacy of either Inhaled Corticosteroids (ICS) or a fixed combination of ICS with a long-acting beta-agonist (bronchodilator) and regular patronage of the pharmacy for the previous six months.
  • Confirmed diagnosis from either the physician's diagnosis or the patient's self-report.
  • No respiratory comorbidities (i.e., COPD or lung diseases).
  • Uses a smartphone (IOS or Android).
  • Ability to communicate with the pharmacist in English.
  • Volunteer to participate in the program for the period.

Критерии исключения

  • The adult patient with asthma aged < 25 years or > 64 years old.
  • The patient with one of the following - coronary heart disease, severe hypertension, severe heart failure, severe musculoskeletal disorder, mental health condition, dementia, chronic obstructive lung disease, or COVID-19.
  • Participating in another "Pharmacy Counseling or Education Program."
  • The patient does not have a smartphone (iOS or Android).
  • The patient does not have sufficient comprehension or the ability to communicate effectively in English.
  • The patient is unwilling or unable to participate in the entire program.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Простое слепое
Основная цель
Организация здравоохранения

Центры проведения

Список центров уточняется — проверьте первичный протокол.

Идентификаторы

NCT: NCT07018583 · NRRU2025-001_DON

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗