scholarly journals Child Welfare Partnership for Research and Training: A Title IV-E University/Community Collaborative Research Model

2013 ◽  
Vol 7 (4) ◽  
pp. 411-429 ◽  
Author(s):  
Laurie Drabble ◽  
Kathy Lemon ◽  
Amy D'Andrade ◽  
Brett Donoviel ◽  
Julia Le
2018 ◽  
Vol 12 (3) ◽  
pp. 281-299 ◽  
Author(s):  
Austin Griffiths ◽  
David Royse ◽  
Kristine Piescher ◽  
Traci LaLiberte

2018 ◽  
Author(s):  
Gwyneth A. MacMillan ◽  
Marianne Falardeau ◽  
Catherine Girard ◽  
Sophie Dufour-Beauséjour ◽  
Justine Lacombe-Bergeron ◽  
...  

For decades, Indigenous voices have called for research practices that are more collaborative and inclusive. At the same time, researchers are becoming aware of the importance of community-collaborative research. However, in Canada, many researchers receive little formal training on how to collaboratively conduct research with Indigenous communities. This is particularly problematic for early-career researchers (ECRs) whose fieldwork often involves interacting with communities. To address this lack of training, two peer-led workshops for Canadian ECRs were organized in 2016 and 2017 with the following objectives: (a) to cultivate awareness about Indigenous cultures, histories and languages; (b) to promote sharing of Indigenous and non-Indigenous ways of knowing; and (c) to foster approaches and explore tools for conducting community collaborative research. Here we present these peer-led Intercultural Indigenous Workshops and discuss workshop outcomes according to five themes: scope and interdisciplinarity, Indigenous representation, workshop environment, skillful moderation and workshop outcomes. We show that peer-led workshops are an effective way for ECRs to cultivate cultural awareness, learn about diverse ways of knowing, and share collaborative research tools and approaches. Developing this skill set is important for ECRs aiming to conduct community-collaborative research, however broader efforts are needed to shift toward more inclusive research paradigms in Canada.


2005 ◽  
Vol 17 (4) ◽  
pp. 400-404 ◽  
Author(s):  
Roger Myrick ◽  
Anthony Lemelle ◽  
Bart Aoki ◽  
Steve Truax ◽  
George Lemp

2017 ◽  
Vol 41 (1) ◽  
pp. 78-95 ◽  
Author(s):  
Joseph Perazzo ◽  
Margaret Rodriguez ◽  
Jackson Currie ◽  
Robert Salata ◽  
Allison R. Webel

Data repositories are a strategy in line with precision medicine and big data initiatives, and are an efficient way to maximize data utility and form collaborative research relationships. Nurse researchers are uniquely positioned to make a valuable contribution using this strategy. The purpose of this article is to present a review of the benefits and challenges associated with developing data repositories, and to describe the process we used to develop and maintain a data repository in HIV research. Systematic planning, data collection, synthesis, and data sharing have enabled us to conduct robust cross-sectional and longitudinal analyses with more than 200 people living with HIV. Our repository building has also led to collaboration and training, both in and out of our organization. We present a pragmatic and affordable way that nurse scientists can build and maintain a data repository, helping us continue to make to our understanding of health phenomena.


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