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1.
J Health Commun ; 22(5): 373-385, 2017 05.
Artigo em Inglês | MEDLINE | ID: mdl-28339327

RESUMO

Clinical trials are essential for developing new and effective treatments and improving patient quality of life; however, many trials cannot answer their primary research questions because they fall short of their recruitment goals. This article reports the results of formative research conducted in two populations, the public and primary care physicians, to identify messages that may raise awareness and increase interest in clinical trials and be used in a national communication campaign. Results suggested that participants were primarily motivated to participate in clinical trials out of a self-interest to help themselves first. Messages illustrated that current treatments were tested via clinical trials, helped normalize trials as routine practices, and reduced concerns over trying something new first. Participants wanted messages that portray trials as state-of-the-art choices that offer some hope, show people like themselves, and are described in a clear, concise manner with actionable steps for them to take. The study revealed some differences in message salience, with healthy audiences exhibiting lower levels of interest. Our results suggest that targeted messages are needed, and that communication with primary health-care providers is an important and necessary component in raising patient awareness of the importance of clinical trials.


Assuntos
Ensaios Clínicos como Assunto , Comunicação em Saúde/métodos , Conhecimentos, Atitudes e Prática em Saúde , Promoção da Saúde/organização & administração , Opinião Pública , Adulto , Feminino , Grupos Focais , Humanos , Masculino , Participação do Paciente/psicologia , Estados Unidos
2.
Int J Stroke ; 10(3): 282-91, 2015 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-25535808

RESUMO

Every year, approximately 62,000 people with stroke and transient ischemic attack are treated in Canadian hospitals. The 2014 update of the Canadian Secondary Prevention of Stroke guideline is a comprehensive summary of current evidence-based recommendations for clinicians in a range of settings, who provide care to patients following stroke. Notable changes in this 5th edition include an emphasis on treating the highest risk patients who present within 48 h of symptom onset with transient or persistent motor or speech symptoms, who need to be transported to the closest emergency department with capacity for advanced stroke care; a recommendation for brain and vascular imaging (of the intra- and extracranial vessels) to be completed urgently using computed tomography/computed tomography angiography; prolonged cardiac monitoring for patients with suspective cardioembolic stroke but without evidence for atrial fibrillation on electrocardiogram or holter monitoring; and de-emphasizing the need for routine echocardiogram. The Canadian Stroke Best Practice Recommendations include a range of supporting materials such as implementation resources to facilitate the adoption of evidence to practice, and related performance measures to enable monitoring of uptake and effectiveness of the recommendations using a standardized approach. The guidelines further emphasize the need for a systems approach to stroke care, involving an interprofessional team, with access to specialists regardless of patient location, and the need to overcome geographical barriers to ensure equity in access within a universal health-care system.


Assuntos
Guias como Assunto , Prevenção Secundária/métodos , Prevenção Secundária/normas , Acidente Vascular Cerebral/prevenção & controle , Pressão Sanguínea , Canadá , Humanos , Estilo de Vida , Metabolismo dos Lipídeos , Inibidores da Agregação Plaquetária/uso terapêutico , Desenvolvimento de Programas/normas , Fatores de Risco , Acidente Vascular Cerebral/epidemiologia
3.
Ethn Dis ; 16(4): 920-5, 2006.
Artigo em Inglês | MEDLINE | ID: mdl-17061747

RESUMO

With the highest prevalence of diabetes in the United States, American Indians and Alaska Natives are at greatest risk for diabetic eye disease (DED), a leading cause of blindness. The National Eye institute (NEI) conducted formative research to understand DED-related knowledge, identify approaches to managing this disease, and design a communication plan to increase awareness and reduce DED among these populations. The NEI conducted qualitative research at five locations in indian country with representatives from national organizations, tribal members, and healthcare providers. While diabetes ranked high on their list of primary community health issues in need of attention, study participants had only a basic level of diabetes-related knowledge, acknowledged the need for DED education, and underscored the importance of the use of interpersonal and culturally appropriate communication strategies. This is the first exploratory qualitative research study to examine the status of diabetic eye disease among American indians and Alaska Natives whose primary purpose was to inform the design of a national DED communication campaign.


Assuntos
Conscientização , Retinopatia Diabética/etnologia , Retinopatia Diabética/etiologia , Indígenas Norte-Americanos/estatística & dados numéricos , Programas Nacionais de Saúde , Educação de Pacientes como Assunto , Adulto , Fatores Etários , Comunicação , Fatores de Confusão Epidemiológicos , Estudos Transversais , Retinopatia Diabética/diagnóstico , Feminino , Conhecimentos, Atitudes e Prática em Saúde , Acessibilidade aos Serviços de Saúde , Necessidades e Demandas de Serviços de Saúde , Humanos , Masculino , Pessoa de Meia-Idade , Avaliação de Programas e Projetos de Saúde , Pesquisa Qualitativa , Estados Unidos/epidemiologia , United States Indian Health Service
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