1,490 research outputs found

    Personality variables that discriminate pseudoseizures patients and epileptic patients used in the 16 PF

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    This project was designed to study the effect of certain personality factors on pseudoseizure patients. It was hypothesized that Factors C and 0 in the 16 Personality Questionnaire could serve as predictor variables for the criterion variable, positive diagnosis of pseudoseizure versus true epileptic seizures. It was also hypothesized that these two groups, pseudoseizure versus epileptic seizure, would differ significantly on a test titled the Sickness Impact Profile. The two scales in this test, psychosocial and physical, were examined. Two discriminant analyses were performed with these two tests being the predictor variables and group membership being the criterion variable. Non-significant results indicated no support for these two hypotheses. Difficulties with reliability of the 16 PF Questionnaire and the small sample size may have contributed to the non-significant results

    Personality variables that discriminate pseudoseizures patients and epileptic patients used in the 16 PF

    Get PDF
    This project was designed to study the effect of certain personality factors on pseudoseizure patients. It was hypothesized that Factors C and O in the 16 Personality Questionnaire could serve as predictor variables for the criterion variable, positive diagnosis of pseudoseizure versus true epileptic seizures. It was also hypothesized that these two groups, pseudoseizure versus epileptic seizure, would differ significantly on a test titled the Sickness Impact Profile. The two scales in this test, psychosocial and physical, were examined. Two discriminant analyses were performed with these two tests being the predictor variables and group membership being the criterion variable. Non-significant results indicated no support for these two hypotheses. Difficulties with rEliaoility of the 16 PF Questionnaire and the small sample size may have contributed to the non-significant results

    In Search of Professional Dispositions that Yield Cultural Relevance in Primary Grade Pedagogy: A Cautionary Tale of One Kindergarten Teacher

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    Primary grade teachers are challenged to establish firm learning foundations for all children, yet for many teachers cultural diversity makes this a complex pedagogical challenge. It is widely assumed that the success with which teachers meet this challenge is reflected in their dispositions toward diversity, and ultimately toward culturally relevant pedagogy as a professional orientation. This article describes a multi-year study of cultural relevance in early mathematics teaching. Using the case of one kindergarten teacher who exhibited positive dispositions toward cultural relevance, the authors examine factors that seemed to work against its adoption in her pedagogy

    Moral Status and the Oversight of Research Involving Chimeric Animals

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    The use of nonhuman animals in research has long been a source of bioethical and scientific debate. We consider the oversight and use of nonhuman animals in chimeric research. We conducted interviews with twelve members of embryonic stem cell research oversight committees, nine members of institutional animal care and use committees, and fourteen scientists involved in human–nonhuman-animal chimeric research in different areas of the United States. Interviews addressed animal welfare and conceptual issues associated with moral status and humanization of nonhuman animals that contain human cells. Our findings suggest that concepts of enhanced moral status and consciousness are not very useful in human–nonhuman-animal chimeric research in part because their meanings are not easily defined, which presents challenges to applying the concepts in research. Instead, scientists and oversight committee members we interviewed seemed to rely on standard assessments of changes in animal welfare when focusing on the ethics of human-animal chimeric research

    Tailoring the process of informed consent in genetic and genomic research

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    Genomic science and associated technologies are facilitating an unprecedented rate of discovery of novel insights into the relationship between human genetic variation and health. The willingness of large numbers of individuals from different ethnic and cultural backgrounds to donate biological samples is one of the major factors behind the success of the ongoing genomic revolution. Although current informed consent documents and processes demonstrate a commitment to ensuring that study participants are well informed of the risks and benefits of participating in genomic studies, there continues to be a need to develop effective new approaches for adequately informing participants of the changing complexities of the scientific and ethical issues that arise in the conduct of genomics research. Examples of these complexities in genomic research include more widespread use of whole-genome sequencing technologies, broad sharing of individual-level data, evolving information technology, the growing demand for the return of genetic results to participants, and changing attitudes about privacy and the expansion of genomics studies to global populations representing diverse cultural, linguistic and socio-economic backgrounds. We highlight and briefly discuss the importance of ten core scientific, cultural and social factors that are particularly relevant to tailoring informed consent in genomic research, and we draw attention to the need for the informed consent document and process to be responsive to the evolving nature of genomic research

    Increasing African American Advance Directives: Implementing the Five Wishes Education Protocol

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    The completion rate of advance directives by older African Americans remains low. This pilot study evaluated attitudes related to African Americans and advance directives and the effectiveness of the Five Wishes Education Protocol to increase completion rates. The researchers used a descriptive, cross-sectional pilot study and convenience sampling. Three group sessions were conducted over a 2-month period at three senior centers. Twenty-two older African Americans participated. The mean total score on the attitude survey indicated that participants were moderately positive towards advance directives. Following the intervention, the completion rate of the advance directive Five Wishes was 77.35% (n=17), and 54.5% (n=12) of the participants provided copies of the Five Wishes advance directives to their healthcare providers
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