Researchers examining peers' behavioral intentions toward students diagnosed with ADHD have frequently used vignettes and asked students to indicate their willingness to engage with an individual described either with or without symptoms of ADHD. The Shared Activities Questionnaire (SAQ-B) is one instrument that has been used to measure students' intentions to engage with students represented in these vignettes. Confirmatory factor analysis results from 183 middle school students supported the three-factor model underlying the SAQ-B, although there were some areas of model misfit. To examine the effects of experimentally manipulating two vignette conditions (describing a peer displaying ADHD symptoms or a peer without these symptoms) on students' responses to items on the SAQ-B, a multiple indicators, multiple causes (MIMIC) analysis was used. Results of the MIMIC analyses identified 4 of the 24 SAQ-B items that exhibited statistically significant uniform differential item functioning between the experimental vignette conditions. Comparisons of the latent variable means between experimental conditions indicated that participants expressed greater willingness to engage with a peer without ADHD symptoms than with one with symptoms on academic activities; no differences were found on the latent variable means for social and recreational activities. Familiarity with ADHD did not have a significant relation to participants' willingness to engage in any of the three types of activities. Implications for practice and research are discussed.
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http://dx.doi.org/10.1016/j.jsp.2013.01.002 | DOI Listing |
AJPM Focus
February 2025
Department of Medicine, University of Alabama, Bermingham, Alabama.
Introduction: Sickle cell disease (SCD) is an inherited blood disorder affecting approximately 100,000 individuals in the U.S. A lack of knowledgeable providers, particularly for adult patients, has led to a significant number of adults without access to high-quality care.
View Article and Find Full Text PDFCamb Q Healthc Ethics
January 2025
Erasmus School of Law and Erasmus School of Health Policy & Management, Erasmus University Rotterdam, Rotterdam, The Netherlands.
Who should decide what passes for disinformation in a liberal democracy? During the COVID-19 pandemic, a committee set up by the Dutch Ministry of Health was actively blocking disinformation. The committee comprised civil servants, communication experts, public health experts, and representatives of commercial online platforms such as Facebook, Twitter, and LinkedIn. To a large extent, vaccine hesitancy was attributed to disinformation, defined as misinformation (or data misinterpreted) with harmful intent.
View Article and Find Full Text PDFBMJ Open
January 2025
Institute for Sport, Physical Education and Health Sciences, Physical Activity for Health Research Centre, University of Edinburgh, Edinburgh, UK.
Objectives: Physical activity referral schemes (PARS) allow healthcare professionals to refer patients for physical activity support. Evidence of effectiveness is equivocal. Public Health Scotland has developed 'physical activity referral standards' that aim to enhance quality, reduce variability in design and delivery and build further evidence of what works.
View Article and Find Full Text PDFMem Cognit
January 2025
Department of Psychology, Technical University of Darmstadt, Darmstadt, Germany.
The accuracy of metacognitive judgments is rarely incentivized in experiments; hence, it depends on the participants' willingness to invest cognitive resources and respond truthfully. According to arguments promoted in economic research that performance cannot reach its full potential without proper motivation, metacognitive abilities might therefore have been underestimated. In two experiments (N = 128 and N = 129), we explored the impact of incentives on the accuracy of judgments of learning (JOLs), memory performance, and cue use in free recall of word lists.
View Article and Find Full Text PDFJ Med Internet Res
January 2025
Institute for Better Health, Trillium Health Partners, Mississauga, ON, Canada.
Background: Patient portals, or secure websites linked to electronic medical records, have emerged as tools to provide patients with timely access to their health information. To support the potential benefits of patient portals such as improved engagement in health care, it is essential to understand how patients and caregivers experience these portals.
Objective: This study aimed to explore patient and caregiver experiences, facilitators, and barriers to accessing and using a patient portal called MyChart during the initial stages of its implementation.
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