Esta página foi traduzida automaticamente e a precisão da tradução não é garantida. Por favor, consulte o versão em inglês para um texto fonte.

CHEST: Uma Colaboração Com Centros de Saúde Comunitários para Implementar SmarT para Asma (CHEST)

4 de setembro de 2026 atualizado por: James Krings, Washington University School of Medicine

CHEST: Uma Colaboração Com Centros Comunitários de Saúde para Implementar SmarT para Asma

Objetivo: Este estudo visa melhorar o tratamento da asma, ajudando os clínicos dos centros de saúde comunitários a prescrever um tratamento recomendado pelas diretrizes, denominado SMART (Terapia Única de Manutenção e Alívio).

Os investigadores fornecerão formação e recursos aos clínicos, darão feedback sobre os padrões de prescrição e disponibilizarão ferramentas educativas para pacientes e profissionais de saúde. Os investigadores irão implementar estes recursos em fases, em várias clínicas. O estudo irá medir quão bem o programa ajuda os clínicos a prescrever a terapia SMART e se reduz as exacerbações da asma nos pacientes.

Visão geral do estudo

Status

Recrutamento

Condições

Intervenção / Tratamento

Descrição detalhada

CHEST é um ensaio clínico randomizado por clusters em degraus híbrido do tipo 1, no qual seis clínicas de centros de saúde comunitários qualificados a nível federal são selecionadas aleatoriamente e iterativamente para fazer uma transição unidirecional do grupo de controlo para o grupo de implementação SMART. A intervenção principal é um pacote de implementação SMART, que contém três componentes: (1) educação a nível do clínico sobre SMART com facilitação/supervisão contínua da prática, (2) auditoria e feedback seriados a nível da clínica e do clínico sobre os padrões de prescrição de inaladores, (3) fornecimento de um auxiliar de educação em papel e online centrado no clínico e no doente, com um plano de ação para a asma congruente com o SMART concebido para doentes com baixa literacia em saúde, e (4) reuniões do comité de operações durante o período de implementação

O estudo está conceptualmente dividido em três fases: (1) a fase de pré-implementação (controlo) focada no desenvolvimento de materiais de implementação e na recolha de dados de base sobre os padrões de prescrição, (2) a fase de implementação ativa, e (3) a pós-implementação, que se focará na avaliação da sustentabilidade e disseminação.

  1. Fase de pré-implementação: A fase de pré-implementação (que durará de 12 a 24 meses por clínica) foi concebida para ser uma linha de base para o estudo. Durante esta fase, nenhuma intervenção específica será introduzida aos clínicos nas clínicas participantes. Esta fase permitirá à equipa do estudo CHEST recolher dados a nível da clínica sobre as práticas atuais de prescrição de cuidados para a asma e os resultados relacionados com a asma.
  2. Fase de implementação ativa: A segunda fase, que durará de 9 a 24 meses por clínica, começará com a introdução do pacote de implementação SMART aos clínicos e funcionários das clínicas IHN participantes.
  3. Fase de pós-implementação: A fase final do estudo é introduzida após a conclusão da implementação ativa do pacote de implementação SMART em todas as clínicas participantes. Na fase de pós-implementação, serão realizadas avaliações formais para avaliar a sustentabilidade do pacote SMART. Além disso, esta fase inclui esforços para disseminar os resultados do estudo. Isto engloba análises do alcance e impacto dos esforços de disseminação, bem como a aplicação prática e adoção dos resultados na comunidade médica em geral.

Tipo de estudo

Intervencional

Inscrição (Estimado)

2000

Estágio

  • Fase 4

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

  • Nome: James Krings, MD MSCI
  • Número de telefone: 3143769452
  • E-mail: kringsj@wustl.edu

Estude backup de contato

Locais de estudo

    • Missouri
      • St Louis, Missouri, Estados Unidos, 63110
        • Recrutamento
        • Washington University in St. Louis School of Medicine
        • Contato:
      • St Louis, Missouri, Estados Unidos, 63104
        • Ainda não está recrutando
        • Affinia healthcare, 2220 Lemp Ave
        • Contato:
      • St Louis, Missouri, Estados Unidos, 63107
        • Recrutamento
        • Affinia healthcare, 4414 North Florissant Avenue
        • Contato:
      • St Louis, Missouri, Estados Unidos, 63111
        • Ainda não está recrutando
        • Family Care Heath Center, 401 Holly Hills Ave
        • Contato:
      • St Louis, Missouri, Estados Unidos, 63106
      • St Louis, Missouri, Estados Unidos, 63110
        • Recrutamento
        • Family Care Heath Center, 4352 Manchester Ave
        • Contato:
      • St Louis, Missouri, Estados Unidos, 63135
        • Recrutamento
        • Affinia healthcare, 3396 Pershall Road,
        • Contato:

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Filho
  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Descrição

A população do estudo pode ser visualizada a nível do cluster (clínica), do clínico, da equipa ou do paciente.

A nível do cluster (clínica): Para ser elegível para participar neste estudo, um cluster (clínica) deve cumprir todos os seguintes critérios:

  1. Participação ativa na Rede de Saúde Integrada de St. Louis para Parcerias Académicas Comunitárias.
  2. Empregar pelo menos 3 clínicos que normalmente tratam asma em adultos (definido como tratar asma de pelo menos um paciente adulto com asma, em média, semanalmente).
  3. Dados fornecidos à Azara para consultas de dados, e
  4. Disposto e capaz de receber todos os componentes do pacote de implementação SMART (ou seja, visita educativa inicial de divulgação, facilitação/supervisão contínua da prática, auditoria e feedback, e fornecimento de educação de auxiliares de educação a nível do paciente e planos de ação SMART para asma e reuniões mensais do comité de operações).

A nível do clínico/equipa clínica:

Para ser elegível para participar neste estudo, um clínico/membro da equipa clínica deve cumprir todos os seguintes critérios:

  1. Fornecimento de um formulário de consentimento informado assinado e datado.
  2. Licenças estaduais atuais de médico, médico assistente, enfermeiro especialista ou assistente médico.
  3. Cuidados regularmente de adultos com asma (o que pode incluir aqueles formados em medicina familiar, medicina interna, obstetrícia/ginecologia e/ou medicina especializada).
  4. Disposto e capaz de integrar o pacote de implementação SMART na sua prática.
  5. Disposto e capaz de participar durante toda a duração do estudo, incluindo os períodos de pré-implementação, implementação ativa e pós-implementação.
  6. Disposto a fornecer dados sobre padrões de prescrição e resultados dos pacientes com asma durante a duração do estudo.

A nível do paciente:

Para ser elegível para participar neste estudo, um paciente deve cumprir todos os seguintes critérios:

  1. Idade ≥12 anos
  2. Diagnóstico de asma, de qualquer gravidade, codificado (ou seja, Classificação Internacional de Doenças [CID]-10-CM: J45**).
  3. O paciente teve ≥2 exacerbações de asma no último ano durante as quais foram prescritos corticosteroides sistémicos, e/ou o episódio contém uma prescrição ativa para um inalador que é congruente com inaladores de corticosteroides inalados (CSI) de dose média (ou superior) ou inaladores de CSI-agonista β de longa duração (LABA) de dose baixa (ou superior) com inaladores concomitantes de agonista β de curta duração para alívio.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição cruzada
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Sem intervenção: Controlo
Durante este período, os padrões de prescrição e os resultados da asma serão observados sem implementação ativa.
Experimental: Active Implementation
The intervention is a SMART implementation bundle delivered at community health centers. It includes (1) clinician education with practice facilitation to support guideline-concordant prescribing and (2) regular audit and feedback on inhaler prescribing patterns (3) workflow integration support, including prescribing preferences, and (4) patient-centered education tools such as instructional videos and a SMART-congruent asthma action plan designed for low health literacy. Educational outreach is co-led by the PI and a certified asthma educator, with quarterly practice facilitation and feedback visits during the active implementation period. All materials are available in paper and digital formats, with continued access to patient tools beyond the intervention. Providers retain full autonomy over prescribing decisions
The intervention is a SMART implementation bundle delivered in Federally Qualified Health Centers. Unlike drug trials, no medication is supplied; providers prescribe according to guidelines. The bundle includes four components: (1) clinician education with practice facilitation, (2) audit and feedback on prescribing, (3) workflow integration support, including prescribing preferences, and (4) patient education tools such as a SMART-aligned asthma action plan and videos tailored for low health literacy

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Clinician-level adoption of the SMART implementation bundle
Prazo: Through study completion, up to 24 months
Proportion of eligible clinicians who adopt all three core components of the SMART implementation bundle Definition of adoption: Clinician-level adoption will be defined as completion and initial use of all three core SMART implementation bundle components: (1) Participation in at least one SMART-focused education and practice facilitation session; (2) Participation in at least one audit-and-feedback session reviewing SMART prescribing performance; and (3) Initial use of SMART patient-centered education tools, defined as documentation and or clinician self-report of the use of the SMART asthma action plan and/or patient education materials during clinical care. Clinicians will be considered eligible if they: (1) are state-licensed physicians, assistant physicians, nurse practitioners, or physician assistants; (2) provide outpatient clinical care to patients aged ≥12 years with asthma at participating clinics; and (3) are actively employed at the clinic during the implementation period
Through study completion, up to 24 months
Clinic-level effectiveness of the SMART implementation bundle, measured as the proportion of SMART-eligible asthma encounters in which SMART is prescribed
Prazo: Through study completion, up to 24 months

Between-group difference in the proportion of SMART-eligible asthma encounters in which SMART is prescribed, comparing implementation vs control periods Unit of analysis: Individual asthma-related clinical encounters among patients aged ≥12 years.

Definition of eligible encounters: Encounters will be classified as SMART-eligible if patients meet study-defined criteria consistent with GINA Step 3-5 treatment, based on exacerbation history and prescribed controller medications, as defined in the study algorithm.

Definition of SMART prescribing: SMART prescribing will be defined as prescription of an inhaled corticosteroid-formoterol inhaler (budesonide-formoterol 160/4.5 µg or mometasone-formoterol 100/6 µg or equivalent) with instructions consistent with use as both maintenance and reliever therapy.

Through study completion, up to 24 months

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Clinic-level Reach: Reach of the SMART implementation bundle
Prazo: Through study completion, up to 24 months

Number and proportion of eligible clinics that participated in ≥1 component of the SMART implementation bundle. Definition of eligible clinics: Clinics within participating health systems (Affinia Healthcare and Family Care Health Centers) will be considered eligible if they provided care to ≥100 patients aged ≥12 years with asthma (ICD-10-CM: J45.xx) during the calendar year preceding implementation (2024).

Definition of reach: Clinics will be classified as "reached" if they participate in ≥1 predefined implementation activity, including kickoff meeting, staff training, workflow integration, clinical decision support deployment, or audit-and-feedback reporting.

Site selection: Final clinic participation will be determined collaboratively by clinic system leadership and the study steering committee based on operational readiness and feasibility.

Through study completion, up to 24 months
Patient-level effectiveness of SMART implementation, measured as the rate of clinic-treated asthma exacerbations and systemic corticosteroid-treated exacerbations
Prazo: Through study completion, up to 24 months

Between-group difference in the rate of asthma exacerbations treated with systemic corticosteroids, comparing implementation vs control periods Definition of asthma exacerbation: An exacerbation will be defined as any of the following:

  1. Prescription of a new systemic corticosteroid associated with an asthma-related clinical encounter (clinic visit, telephone encounter, or telehealth encounter), identified in the electronic health record;
  2. Encounter with a diagnosis code for acute asthma exacerbation (ICD-10-CM: J45.901); or
  3. Dispensing of a systemic corticosteroid (e.g., prednisone, prednisolone, methylprednisolone, dexamethasone) identified through linkage with Missouri Medicaid (MO HealthNet) pharmacy claims data among enrolled patients.
Through study completion, up to 24 months
Clinician-level Reach: Reach of the SMART implementation bundle
Prazo: Through study completion, up to 24 months

Number and proportion of eligible clinicians who participate in ≥1 SMART implementation activity. Definition of eligible clinicians: Clinicians will be considered eligible if they: (1) are physicians, nurse practitioners, or physician assistants; (2) are actively employed at a participating clinic during the implementation period; and (3) provided care to ≥10 patients aged ≥12 years with asthma (ICD-10-CM: J45.xx) during the 12 months preceding implementation. Eligible clinicians may include those practicing in primary care, pediatrics, pulmonology, allergy/immunology, and obstetrics/gynecology settings.

Definition of reach: Clinicians will be classified as "reached" if they participate in ≥1 predefined implementation activity, including attendance at implementation kickoff meetings, educational sessions, practice facilitation encounters, audit-and-feedback sessions, or engagement with implementation tools (e.g., asthma action plans, clinical decision support, or training materials).

Through study completion, up to 24 months
Staff-level Reach: Reach of the SMART implementation bundle
Prazo: Through study completion, up to 24 months

Number and proportion of eligible staff who participate in ≥1 SMART implementation activity. Definition of eligible staff: Staff will be considered eligible if they: (1) are actively employed at a participating clinic during the implementation period; and (2) directly support clinical care delivery for patients aged ≥12 years with asthma. Eligible staff may include nurses, medical assistants, pharmacists, respiratory therapists, pharmacy technicians, care coordinators, and other staff involved in asthma-related clinical workflows, as determined by clinic leadership and study personnel.

Definition of reach: Staff will be classified as "reached" if they participate in ≥1 predefined implementation activity, including attendance at implementation kickoff meetings, educational sessions, practice facilitation encounters, workflow redesign activities, audit-and-feedback sessions, or engagement with implementation tools

Through study completion, up to 24 months
Patient-level Reach: Reach of SMART among eligible patients
Prazo: Through study completion, up to 24 months

Number and proportion of eligible patients prescribed SMART during the implementation period

Definition of eligible patients: Patients will be considered eligible if they: (1) are aged ≥12 years; (2) received care at a participating clinic during the implementation period; and (3) meet the study-defined definition of moderate-to-severe asthma based on diagnosis codes, medication use, and/or exacerbation history as defined in the study protocol.

Definition of reach: Patients will be classified as "reached" if they receive ≥1 prescription for an inhaled corticosteroid-formoterol inhaler prescribed for use as both maintenance and reliever therapy (SMART) during the implementation period. Eligible SMART prescriptions include budesonide-formoterol or mometasone-formoterol prescribed at guideline-consistent dosing for maintenance and reliever use, consistent with GINA recommendations.

Through study completion, up to 24 months
Patient-level safety of SMART therapy (adverse events of special interest and serious adverse events)
Prazo: Through study completion, up to 24 months

Between-group difference in the rate of adverse events of special interest (AESI) and serious adverse events (SAEs), comparing implementation vs control periods Adverse events of special interest (AESI): AESI will include known or anticipated adverse effects potentially associated with inhaled corticosteroid-formoterol therapy, identified using diagnosis codes and/or documented clinical events, including:

  • Oral candidiasis (ICD-10-CM: B37.0)
  • Dysphonia (ICD-10-CM: R49.0)
  • Tremor (ICD-10-CM: R25.1, G25.0, G25.2)
  • Palpitations (ICD-10-CM: R00.2)

Serious adverse events (SAEs): SAEs will be defined according to standard regulatory criteria, including death, life-threatening event, inpatient hospitalization or prolongation of hospitalization, persistent or significant disability/incapacity, or other medically important events potentially related to asthma therapy.

Through study completion, up to 24 months
Clinician-level effectiveness of the SMART implementation bundle, measured as the proportion of clinicians classified as frequent SMART prescribers
Prazo: Through study completion, up to 24 months
Proportion of eligible clinicians classified as frequent SMART prescribers, defined as prescribing SMART in ≥30% of SMART-eligible encounters Definition of eligible clinicians: Clinicians will be considered eligible if they: (1) are physicians, nurse practitioners, or physician assistants; (2) are actively employed at a participating clinic during the implementation period; and (3) managed ≥10 patients aged ≥12 years with moderate-to-severe asthma during the 12 months preceding implementation initiation. Definition of SMART-eligible encounters: Encounters will be classified as SMART-eligible if patients meet study-defined criteria consistent with GINA Step 3-5 treatment, based on exacerbation history and prescribed controller medications, as defined in the study algorithm. Definition of SMART prescribing: SMART prescribing will be defined as the prescription of an inhaled corticosteroid-formoterol inhaler with instructions consistent with use as both maintenance and reliever therapy.
Through study completion, up to 24 months
Clinician-level adherence to the SMART implementation bundle (implementation strategy adherence)
Prazo: Through study completion, up to 24 months

Proportion of eligible clinicians meeting predefined adherence thresholds to implementation bundle components.

Definition of implementation adherence: Clinician adherence to the implementation bundle will be defined as meeting all of the following criteria: (1) Participation in the baseline implementation visit; (2) Participation in ≥50% of offered practice facilitation sessions; (3) Participation in ≥50% of offered audit-and-feedback sessions; and (4) Self-reported use of SMART patient education tools (SMART asthma action plan and/or patient education materials) in ≥50% of SMART-eligible encounters.

Definition of eligible clinicians: Eligible clinicians will include physicians, assistant physicians, nurse practitioners, and physician assistants actively employed at participating clinics who manage patients aged ≥12 years with asthma.

Through study completion, up to 24 months
Clinician-level fidelity to SMART prescribing and delivery (clinical intervention fidelity)
Prazo: Through study completion, up to 24 months

Proportion of clinicians and sampled encounters in which SMART was delivered consistent with recommended clinical practice Definition of fidelity: Fidelity will be defined as clinician-reported delivery of SMART therapy consistent with recommended clinical practice, including:

  1. Prescription of an ICS-formoterol inhaler intended for both maintenance and reliever use;
  2. Discontinuation or intentional non-prescribing of short-acting beta-agonist (SABA) rescue inhalers when appropriate; and
  3. Provision of SMART-specific patient education, including asthma action plan use and instruction on SMART dosing.

Assessment method: Fidelity will be assessed using structured clinician fidelity assessments conducted by study personnel. A random sample of approximately 50 SMART-prescribing encounters across participating clinicians will be selected, and clinicians will be asked to confirm whether SMART was delivered consistent with recommended clinical practice.

Through study completion, up to 24 months
System-level implementation cost and budget impact of the SMART implementation bundle
Prazo: Through study completion, up to 24 months

Estimated implementation costs and exploratory budget impact associated with implementation of the SMART implementation bundle and asthma-related healthcare utilization Objective: To estimate the cost of implementing the SMART implementation bundle and assess the exploratory budget impact of SMART adoption on asthma-related healthcare costs from healthcare system and payer perspectives.

Implementation cost assessment: Implementation costs will be estimated using micro-costing methods and will include: • Personnel time associated with implementation activities (education sessions, practice facilitation, audit-and-feedback delivery, and coordination); • Training and educational material development and dissemination costs; • Implementation infrastructure and operational costs; and • Administrative and implementation support costs borne by participating clinics and the study team.

Through study completion, up to 24 months
Patient-level sustainment of SMART prescribing and asthma outcomes following completion of active implementation (maintenance outcome)
Prazo: Through study completion, up to 24 months

Proportion of SMART-eligible encounters prescribed SMART and rate of asthma exacerbations during the sustainment period compared with the active implementation period Definition of sustainment period: The sustainment period will be defined as the period following completion of active implementation activities (e.g., cessation of structured practice facilitation and audit-and-feedback sessions), during which clinics continue routine clinical care without active implementation support.

Primary sustainment measures: Sustainment will be assessed by comparing:

  1. The proportion of SMART-eligible encounters in which SMART is prescribed during the sustainment period compared with the active implementation period; and
  2. The rate of asthma exacerbations (defined as systemic corticosteroid-treated exacerbations or exacerbation-related encounters) during the sustainment period compared with the active implementation period.
Through study completion, up to 24 months
Clinician-level and system-level sustainment of the SMART implementation bundle and organizational capacity to maintain SMART clinical practice (implementation sustainment outcome)
Prazo: Through study completion, up to 24 months

Continued use of SMART implementation bundle components following completion of active implementation support

Definition of sustainment: Sustainment will be defined as the continued use of SMART implementation bundle components during the sustainment period, including ongoing use of SMART asthma action plans, continued incorporation of SMART into clinical workflows, and continued engagement with SMART-related clinical practices in the absence of active implementation support.

Sustainment capacity assessment: A validated sustainability assessment instrument, such as the Clinical Sustainability Assessment Tool (CSAT), will be administered to clinic leadership, site champions, and clinical staff at the beginning and conclusion of the sustainment period to assess organizational capacity to maintain SMART implementation.

Through study completion, up to 24 months
Patient-level de-implementation of SABA prescribing among patients prescribed SMART (de-implementation outcome)
Prazo: Through study completion, up to 24 months

Proportion of SMART-prescribing encounters in which SABA inhalers are not concurrently prescribed

Definition of de-implementation: De-implementation will be defined as the absence of an active SABA prescription following initiation of SMART therapy or documented discontinuation of an existing SABA prescription at the time SMART is prescribed.

Eligible encounters: All clinical encounters in which SMART is prescribed for maintenance and reliever therapy (ICS-formoterol prescribed for both maintenance and reliever use).

Objective: This outcome assesses the extent to which SMART implementation replaces legacy SABA prescribing practices consistent with guideline-recommended care.

Through study completion, up to 24 months

Outras medidas de resultado

Medida de resultado
Descrição da medida
Prazo
Qualitative assessment of the determinants of patient-level reach of SMART (CFIR-informed)
Prazo: Through study completion, up to 24 months

Identification of barriers and facilitators influencing patient receipt and use of SMART therapy Objective: To identify patient-level determinants influencing receipt and use of SMART therapy among eligible patients, guided by the Consolidated Framework for Implementation Research (CFIR).

Participant recruitment: A purposive sample of eligible patients aged ≥12 years with moderate-to-severe asthma will be invited to participate in semi-structured interviews and/or focus groups. Sampling will include patients who: (1) were prescribed SMART and use it consistently; (2) were prescribed SMART but do not use it consistently; and (3) were eligible for SMART but were not prescribed SMART. This sampling strategy will ensure representation of diverse experiences with SMART implementation.

Through study completion, up to 24 months
Qualitative assessment of the determinants of clinician- and staff-level reach of the SMART implementation bundle (CFIR-informed)
Prazo: Through study completion, up to 24 months

Identification of barriers and facilitators influencing clinician and staff participation in SMART implementation activities Objective: To identify multilevel determinants influencing clinician and staff participation ("reach") in the SMART implementation bundle, guided by the Consolidated Framework for Implementation Research (CFIR).

Participant recruitment: All eligible clinicians, staff, and clinic leadership at participating sites will be invited to complete structured surveys assessing participation and determinants of participation. A purposive sample of clinicians, staff, and clinic leaders representing high, moderate, and low levels of implementation participation will be invited to participate in semi-structured interviews and/or focus groups. Snowball sampling may be used to identify additional individuals with relevant perspectives.

Through study completion, up to 24 months
Digital reach of SMART implementation materials, including the CHEST study website and SMART asthma action plan (AAP)
Prazo: Through study completion, up to 24 months

Number of unique website users, number of website sessions, number of SMART asthma action plan (AAP) downloads, and number of views of SMART-related implementation materials Definition of digital reach: Digital reach will be defined as engagement with the CHEST study website and associated SMART implementation resources by any website user. Metrics will include: (1) number of unique users accessing the website; (2) number of website sessions; (3) number of page views of SMART-related materials; and (4) number of downloads of the SMART asthma action plan (AAP).

Outcome definition: The primary dissemination reach outcomes will include cumulative and monthly counts of website access and SMART AAP downloads. Secondary descriptive metrics will include user engagement trends over time.

Through study completion, up to 24 months
Qualitative assessment of clinician and staff perceptions of the effectiveness of the SMART implementation bundle and SMART therapy (CFIR-informed exploratory outcome)
Prazo: Through study completion, up to 24 months

Identification of clinician and staff perceptions of the effects of the SMART implementation bundle on workflow, prescribing behavior, knowledge, self-efficacy, and asthma care delivery Objective: To assess clinician and staff perceptions of the effectiveness and impact of the SMART implementation bundle and SMART therapy, guided by the Consolidated Framework for Implementation Research (CFIR).

Participant recruitment: All eligible clinic leadership, clinicians, and staff will be invited to complete structured surveys assessing perceived effects of the implementation bundle. A purposive sample of clinicians, staff, and clinic leaders representing varying levels of implementation engagement and SMART prescribing will be invited to participate in semi-structured interviews and/or focus groups. Snowball sampling may be used to identify additional participants with relevant perspectives.

Through study completion, up to 24 months
Qualitative assessment of patient perceptions of the effectiveness and impact of the SMART implementation bundle and SMART therapy (CFIR-informed exploratory outcome)
Prazo: Through study completion, up to 24 months

Identification of patient perceptions of the effects of SMART therapy and associated implementation efforts on asthma management, treatment confidence, self-efficacy, usability, and satisfaction

Objective: To assess patient perceptions of the effectiveness and impact of SMART therapy and the SMART implementation bundle on asthma self-management and care delivery.

Participant recruitment: A purposive sample of eligible patients aged ≥12 years with moderate-to-severe asthma receiving care at participating clinics will be invited to participate in semi-structured interviews and/or focus groups. Sampling will include patients who were prescribed SMART and patients eligible for SMART but not prescribed SMART to capture diverse perspectives. Site CMOs, site champions, and study personnel may assist with identifying eligible participants. Snowball sampling may be used to identify additional participants with relevant perspectives.

Through study completion, up to 24 months
Qualitative assessment of clinician and staff adoption of the SMART implementation bundle (CFIR-informed exploratory outcome)
Prazo: Through study completion, up to 24 months

Identification of clinician and staff perspectives on adoption of the SMART implementation bundle, including reasons for participation, non-participation, and variation in adoption across implementation components Objective: To assess clinician and staff perspectives on adoption of the SMART implementation bundle and identify barriers and facilitators influencing uptake.

Participant recruitment: A purposive sample of clinic leadership, clinicians, and staff eligible for participation in the SMART implementation bundle will be invited to participate in semi-structured interviews and/or focus groups. Participants will be selected to represent a range of adoption levels, including early adopters, delayed adopters, and non-adopters. Site CMOs, site champions, and study personnel may assist with identifying eligible participants. Snowball sampling may be used to identify additional participants with relevant perspectives.

Through study completion, up to 24 months

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Publicações e links úteis

A pessoa responsável por inserir informações sobre o estudo fornece voluntariamente essas publicações. Estes podem ser sobre qualquer coisa relacionada ao estudo.

Publicações Gerais

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

6 de janeiro de 2026

Conclusão Primária (Estimado)

15 de novembro de 2027

Conclusão do estudo (Estimado)

15 de novembro de 2028

Datas de inscrição no estudo

Enviado pela primeira vez

7 de novembro de 2025

Enviado pela primeira vez que atendeu aos critérios de CQ

19 de novembro de 2025

Primeira postagem (Real)

21 de novembro de 2025

Atualizações de registro de estudo

Última Atualização Postada (Real)

10 de setembro de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

4 de setembro de 2026

Última verificação

1 de setembro de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

SIM

Descrição do plano IPD

Sim. Serão partilhados DIP anonimizados, incluindo dados quantitativos (dados demográficos, questionários validados, registos de presenças e dados anonimizados de EHR sobre consultas de asma, diagnósticos e prescrições) e transcrições de entrevistas qualitativas e grupos focais verificadas quanto à precisão e anonimizadas. O protocolo, o plano de análise estatística, o dicionário de dados e o código analítico também serão partilhados através do BioLINCC da NHLBI. Os dados serão armazenados de forma segura no REDCap da WUSM, RIS ou Box antes de serem partilhados. A transcrição compatível com HIPAA e a validação REDCap garantem a precisão. A supervisão e conformidade serão mantidas através do IRB da WUSM, do Gabinete de Segurança da Informação, dos órgãos reguladores dos centros de saúde comunitários e do DSMB do estudo. Os dados seguirão os padrões COREQ, CONSORT e TIDieR e serão partilhados após a publicação primária.

Prazo de Compartilhamento de IPD

Os DPI anonimizados e os materiais de suporte serão submetidos ao BioLINCC do NHLBI no prazo de 12 meses após a conclusão da recolha de dados ou antes da publicação primária, o que ocorrer primeiro. Os dados serão submetidos a uma revisão de qualidade e conformidade antes da disponibilização pública. Os dados partilhados permanecerão arquivados e acessíveis para preservação a longo prazo no BioLINCC, de acordo com as práticas de repositório do NIH e do NHLBI, para permitir futuras análises secundárias e estudos de replicação.

Critérios de acesso de compartilhamento IPD

Os dados de participantes individuais anonimizados e os materiais de suporte serão partilhados através do repositório BioLINCC do NHLBI. O acesso será aberto a investigadores qualificados sem restrições para investigação, replicação ou análises secundárias consistentes com os objetivos do estudo e os interesses de saúde pública. As proteções de privacidade e confidencialidade serão mantidas de acordo com as aprovações do IRB da WUSM, do Gabinete de Segurança da Informação, dos organismos reguladores dos centros de saúde comunitários e do DSMB do estudo. Os pedidos de dados serão revistos e geridos através dos procedimentos padrão do BioLINCC, que requerem a submissão de um pedido de dados e a execução de um Acordo de Distribuição de Materiais de Investigação. A supervisão da conformidade e a proteção contínua da confidencialidade dos participantes serão asseguradas através dos mecanismos de supervisão regulatória da WUSM e do NHLBI.

Tipo de informação de suporte de compartilhamento de IPD

  • PROTOCOLO DE ESTUDO
  • SEIVA
  • CIF
  • ANALYTIC_CODE
  • CSR

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

Se inscrever