scholarly journals Sociolinguistic Diversity Can Boost Cognitive Functions

2021 ◽  
Author(s):  
Yin Jue Chang

This study investigates the link between sociolinguistic diversity and executive functions. 127 healthy adults from Malaysia were recruited to complete three cognitive tasks and the Contextual Linguistic Profile Questionnaire (CLiP-Q). A sociolinguistic diversity score was derived for each participant, with a higher score reflecting a greater exposure and use of diverse languages both at the individual and the societal level. The results demonstrated a sociolinguistic diversity advantage in cognitive functions. Higher sociolinguistic diversity scores were associated with lesser interference in the Flanker task and better accuracy in the 2-back task. Additionally, a significant interaction between sociolinguistic diversity and socioeconomic status was found for the set-shifting task, showing that sociolinguistic diversity could reduce mixing costs and improve set-shifting task accuracy for low socioeconomic status participants who are usually disadvantaged in cognitive control. Thus, it is important for research in the multilingualism field to take sociolinguistic diversity context into account.

2017 ◽  
Vol 8 (3) ◽  
pp. 169-175 ◽  
Author(s):  
Nicholas C. Arpey ◽  
Anne H. Gaglioti ◽  
Marcy E. Rosenbaum

Introduction: Clinician perceptions of patients with low socioeconomic status (SES) have been shown to affect clinical decision making and health care delivery in this group. However, it is unknown how and if low SES patients perceive clinician bias might affect their health care. Methods: In-depth interviews with 80 enrollees in a state Medicaid program were analyzed to identify recurrent themes in their perceptions of care. Results: Most subjects perceived that their SES affected their health care. Common themes included treatment provided, access to care, and patient-provider interaction. Discussion: This study highlights complex perceptions patients have around how SES affects their health care. These results offer opportunities to reduce health care disparities through better understanding of their impact on the individual patient-provider relationship. This work may inform interventions that promote health equity via a multifaceted approach, which targets both providers and the health care system as a whole.


2000 ◽  
Vol 66 (4) ◽  
pp. 491-508 ◽  
Author(s):  
Paddy C. Favazza ◽  
Leslie Phillipsen ◽  
Poonam Kumar

The results of two studies are presented: (a) an examination of the reliability of the Acceptance Scale for Kindergartners with a sample of non-Caucasian, low socioeconomic status (SES) children, and (b) the efficacy of an intervention designed to promote acceptance of young children with disabilities with this new sample. Results indicate that the Acceptance Scale for Kindergarten—Revised is reliable and that various components of a special friends intervention yield differential results. Specifically, results indicate that children exposed to individual components of the intervention had short-term gains in acceptance of individuals with disabilities, while children exposed to the whole intervention had short-term and long-term gains in acceptance. Exposure to the whole program is more effective than any of the individual components in producing greater changes in levels of acceptance of young children with disabilities.


2014 ◽  
Author(s):  
Sarah Dayle Herrmann ◽  
Jessica Bodford ◽  
Robert Adelman ◽  
Oliver Graudejus ◽  
Morris Okun ◽  
...  

2020 ◽  
Vol 91 (6) ◽  
pp. 2042-2062
Author(s):  
Susana Mendive ◽  
Mayra Mascareño Lara ◽  
Daniela Aldoney ◽  
J. Carola Pérez ◽  
José P. Pezoa

BMJ Open ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. e043547
Author(s):  
Donald A Redelmeier ◽  
Kelvin Ng ◽  
Deva Thiruchelvam ◽  
Eldar Shafir

ObjectivesEconomic constraints are a common explanation of why patients with low socioeconomic status tend to experience less access to medical care. We tested whether the decreased care extends to medical assistance in dying in a healthcare system with no direct economic constraints.DesignPopulation-based case–control study of adults who died.SettingOntario, Canada, between 1 June 2016 and 1 June 2019.PatientsPatients receiving palliative care under universal insurance with no user fees.ExposurePatient’s socioeconomic status identified using standardised quintiles.Main outcome measureWhether the patient received medical assistance in dying.ResultsA total of 50 096 palliative care patients died, of whom 920 received medical assistance in dying (cases) and 49 176 did not receive medical assistance in dying (controls). Medical assistance in dying was less frequent for patients with low socioeconomic status (166 of 11 008=1.5%) than for patients with high socioeconomic status (227 of 9277=2.4%). This equalled a 39% decreased odds of receiving medical assistance in dying associated with low socioeconomic status (OR=0.61, 95% CI 0.50 to 0.75, p<0.001). The relative decrease was evident across diverse patient groups and after adjusting for age, sex, home location, malignancy diagnosis, healthcare utilisation and overall frailty. The findings also replicated in a subgroup analysis that matched patients on responsible physician, a sensitivity analysis based on a different socioeconomic measure of low-income status and a confirmation study using a randomised survey design.ConclusionsPatients with low socioeconomic status are less likely to receive medical assistance in dying under universal health insurance. An awareness of this imbalance may help in understanding patient decisions in less extreme clinical settings.


Author(s):  
Kevin Kien Hoa Chung ◽  
Xiaomin Li ◽  
Cheuk Yi Lam ◽  
Chun Bun Lam ◽  
Wing Kai Fung ◽  
...  

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