2020
DOI: 10.1017/cts.2020.552
|View full text |Cite
|
Sign up to set email alerts
|

How engagement of a diverse set of stakeholders shaped the design, implementation, and dissemination of a multicenter pragmatic trial of stroke transitional care: The COMPASS study

Abstract: This version may be subject to change during the production process.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2

Citation Types

0
4
0

Year Published

2022
2022
2024
2024

Publication Types

Select...
3

Relationship

0
3

Authors

Journals

citations
Cited by 3 publications
(4 citation statements)
references
References 26 publications
0
4
0
Order By: Relevance
“…Gesell 2021 (Literature article) [51] Created a statewide stakeholder committee to contribute to design, conduct, and dissemination of findings of a multicenter pragmatic clinical trial. The committee added, shaped, and refined intervention components and all patient-and provider-facing materials.…”
Section: Data Source Patient Engagement Level: Cooperation Examples (...mentioning
confidence: 99%
See 1 more Smart Citation
“…Gesell 2021 (Literature article) [51] Created a statewide stakeholder committee to contribute to design, conduct, and dissemination of findings of a multicenter pragmatic clinical trial. The committee added, shaped, and refined intervention components and all patient-and provider-facing materials.…”
Section: Data Source Patient Engagement Level: Cooperation Examples (...mentioning
confidence: 99%
“…For example, many of the activities categorized under "coordination"-a lower intensity engagement activity-and "collaboration"-a higher intensity engagement activity-involved assembling patient advisory groups. Upon closer review, there were processes and roles in those activities we considered collaboration that signaled a deeper, longer, and more patient-centered approach, such as being involved in all phases of implementation (e.g., Browne 2020, literature article), [48] serving in roles with more power or voice (e.g., Participant Interview 1), and patients seeing how their input was incorporated (e.g., Gesell 2021, literature article) [51].…”
Section: Data Source Patient Engagement Level: Community-based Partic...mentioning
confidence: 99%
“…Community-academic partnerships facilitate different voices and perspectives at all phases of the research process, from design to dissemination. The co-creation of knowledge via the engagement of relevant stakeholders in an active and committed decision-making process about a health issue is expected to lead to more meaningful research outcomes for patients, care providers, and communities [ 8 , 11 , 12 ].…”
Section: Introductionmentioning
confidence: 99%
“…The active dissemination of research that prioritises interactions with non-academic stakeholders is a core principle of CBPR [ 20 ]. However, literature reporting specific outputs from community dissemination is still scarce [ 8 , 11 , 20 , 21 ]. The contributions of non-academic stakeholders are described less frequently in reports on dissemination and implementation research [ 8 ].…”
Section: Introductionmentioning
confidence: 99%