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2021 ◽  
Vol 50 (1) ◽  
pp. 271-271
Author(s):  
Jared Ward ◽  
Adam Green ◽  
Stanley Dumond ◽  
Jessica Clough ◽  
Robert Cole ◽  
...  

Author(s):  
Cândida Fonseca ◽  
Paulo Bettencourt ◽  
Dulce Brito ◽  
Helena Febra ◽  
Álvaro Pereira ◽  
...  

Author(s):  
Edwin Afriyie

This paper is an investigation of the efficacy of hymns and their impact on personality. The investigation was aimed at addressing ‘the problem of the relationship of hymnody and discipline, self-regulation which results in guarded behaviour reflecting in speech, personal appearance, and conduct within the Ghanaian society.’ The investigation was against the backdrop of the perception that hymnody influences devoted singers with the power to shape personality and bring about character transformation. The objective of the investigation was to spike the hymnody effect within society. The theory of personal transformation combined the qualitative design. The study consisted of a single question to determine the most predominant view about hymnody in hymn-singing churches in Accra and Kumasi. Findings indicated that 41% of 300 informants confirmed hymnody as powerful and transformative, but elitist and excluded the non-literate. Eurocentric and Afrocentric perspectives attended the analysis of Hymnody. The study concluded that hymnody is beneficial to mood and character change to stimulate the transformation of soul and mind, leading to the growth of the inner man as a function of discipline. Thus, a reference to the notions of pedagogy and discipline are underscored as transforming outcomes of devoted hymnody participation. The paper’s contribution to knowledge lies in its focus on the role of hymnody, a religious ritual, as catalyzing the development of the discipline ethic to engage the attention of the academy for further research. Keywords: Discipline, Ghana, Hymnody, Personality.


BMC Cancer ◽  
2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Deborah Cragun ◽  
Jason Beckstead ◽  
Meagan Farmer ◽  
Gillian Hooker ◽  
Marleah Dean ◽  
...  

Abstract Background Implementing genetic testing for inherited cancer predisposition into routine clinical care offers a tremendous opportunity for cancer prevention and early detection. However, genetic testing itself does not improve outcomes; rather, outcomes depend on implemented follow-up care. The IMPACT study is a hybrid type I randomized effectiveness-implementation trial to simultaneously evaluate the effectiveness of two interventions for individuals with inherited cancer predisposition focused on: 1) increasing family communication (FC) of genetic test results; and 2) improving engagement with guideline-based cancer risk management (CRM). Methods This prospective study will recruit a racially, geographically, and socioeconomically diverse population of individuals with a documented pathogenic/likely pathogenic (P/LP) variant in an inherited cancer gene. Eligible participants will be asked to complete an initial trial survey and randomly assigned to one of three arms: A) GeneSHARE, a website designed to increase FC of genetic test results; B) My Gene Counsel’s Living Lab Report, a digital tool designed to improve understanding of genetic test results and next steps, including CRM guidelines; or C) a control arm in which participants continue receiving standard care. Follow-up surveys will be conducted at 1, 3, and 12 months following randomization. These surveys include single-item measures, scales, and indices related to: 1) FC and CRM behaviors and behavioral factors following the COM-B theoretical framework (i.e., capability, opportunity, and motivation); 2) implementation outcomes (i.e., acceptability, appropriateness, exposure, and reach); and 3) other contextual factors (i.e., sociodemographic and clinical factors, and uncertainty, distress, and positive aspects of genetic test results). The primary outcomes are an increase in FC of genetic test results (Arm A) and improved engagement with guideline-based CRM without overtreatment or undertreatment (Arm B) by the 12-month follow-up survey. Discussion Our interventions are designed to shift the paradigm by which individuals with P/LP variants in inherited cancer genes are provided with information to enhance FC of genetic test results and engagement with guideline-based CRM. The information gathered through evaluating the effectiveness and implementation of these real-world approaches is needed to modify and scale up adaptive, stepped interventions that have the potential to maximize FC and CRM. Trial registration This study is registered at Clinicaltrials.gov (NCT04763915, date registered: February 21, 2021). Protocol version September 17th, 2021 Amendment Number 04.


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