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1.
J Am Med Inform Assoc ; 18(1): 24-31, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-21169619

RESUMO

OBJECTIVE: Informatics applications have the potential to improve participation in clinical trials, but their design must be based on user-centered research. This research used a fully counterbalanced experimental design to investigate the effect of changes made to the original version of a website, http://BreastCancerTrials.org/, and confirm that the revised version addressed and reinforced patients' needs and expectations. DESIGN: Participants included women who had received a breast cancer diagnosis within the last 5 years (N=77). They were randomized into two groups: one group used and reviewed the original version first followed by the redesigned version, and the other group used and reviewed them in reverse order. MEASUREMENTS: The study used both quantitative and qualitative measures. During use, participants' click paths and general reactions were observed. After use, participants were asked to answer survey items and open-ended questions to indicate their reactions and which version they preferred and met their needs and expectations better. RESULTS: Overall, the revised version of the site was preferred and perceived to be clearer, easier to navigate, more trustworthy and credible, and more private and safe overall. However, users who viewed the original version last had similar attitudes toward both versions. CONCLUSION: By applying research findings to the redesign of a website for clinical trial searching, it was possible to re-engineer the interface to better support patients' decisions to participate in clinical trials. The mechanisms of action in this case appeared to revolve around creating an environment that supported a sense of personal control and decisional autonomy.


Assuntos
Neoplasias da Mama/terapia , Ensaios Clínicos como Assunto , Informação de Saúde ao Consumidor , Internet , Preferência do Paciente , Seleção de Pacientes , Adulto , Idoso , Feminino , Pesquisa sobre Serviços de Saúde/métodos , Humanos , Pessoa de Meia-Idade , Satisfação do Paciente , Desenvolvimento de Programas , Método Simples-Cego , Estados Unidos , Interface Usuário-Computador
2.
J Med Internet Res ; 9(2): e13, 2007 May 15.
Artigo em Inglês | MEDLINE | ID: mdl-17513284

RESUMO

BACKGROUND: Internet-based clinical trial matching systems have the potential to streamline the search process for women with breast cancer seeking alternative treatments. A prototype system was developed to leverage the capabilities of a personal health record system for the purpose of identifying clinical trials. OBJECTIVE: This study examines how breast cancer patients perceive and interact with a preliminary version of an Internet-based clinical trial matching system, while taking into account the demands of diagnosis and treatment decision making. METHODS: Breast cancer patients participated in small group discussions and interacted with the prototype website in a two-phase qualitative research process. The first phase explored the experience of breast cancer patients (n = 8) with treatment decision making, initial responses to the idea of Internet-based clinical trial matching systems, and reactions to the prototype site. In the second phase, a different set of breast cancer patients (n = 7) reviewed revised website content and presentation and participated in a usability test in which they registered on the system and completed a personal health record to set up the matching process. RESULTS: Participants were initially skeptical of the prototype system because it emphasized registration, had a complicated registration process, and asked for complex medical information. Changing content and attending to usability guidelines improved the experience for women in the second phase of the research and enabled the identification of functionality and content issues, such as lack of clear information and directions on how to use the system. CONCLUSIONS: This study showed that women felt favorably about the idea of using the Internet to search for clinical trials but that such a system needed to meet their expectations for credibility and privacy and be sensitive to their situation. Developers can meet these expectations by conforming to established usability guidelines and testing improvements with breast cancer patients. Future research is needed to verify these findings and to continue to improve systems of this nature.


Assuntos
Neoplasias da Mama/terapia , Ensaios Clínicos como Assunto , Internet , Adulto , Idoso , Tomada de Decisões , Feminino , Humanos , Entrevistas como Assunto , Prontuários Médicos , Pessoa de Meia-Idade , Seleção de Pacientes , Pesquisa Qualitativa , Interface Usuário-Computador
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