Anneliese Synnot
Datos Biográficos
| ID | 177605 |
|---|---|
| NOMBRE | Anneliese Synnot |
| NOMBRES | Anneliese |
| APELLIDO | Synnot |
| FIRMA | SYNNOT A |
| AFILIACIONES | La Trobe University, Bundoora, Victoria, Australia |
| ORCID | 0000-0002-4008-4208 |
| VERIFICADO | Sí |
| TOTAL DE OBRAS | 6 |
| TOTAL DE CITAS | 14 |
| TOTAL COMO AUTOR | 6 |
| TOTAL COMO EDITOR | 0 |
| PRIMER AÑO DE PUBLICACIÓN | 2014 |
| AÑO MÁS RECIENTE DE PUBLICACIÓN | 2021 |
| ÍNDICE H | 2 |
Stakeholder Involvement in Systematic Reviews
Case study 1 describes stakeholder involvement in setting systematic review priorities
Health-related quality of life after traumatic brain injury
By transforming the QOLIBRI-OS into utility scores, we enabled the application in economic evaluations and in summary measures of population health, which may be used to inform decision-makers on the best interventions and strategies for TBI patients
The evolution of Cochrane evidence summaries in health communication and participation
Knowledge translation resources that summarise and disseminate systematic review findings can support evidence into policy and practice. Since 2007, we have produced Evidence Bulletins; brief, web-based summaries of Cochrane Reviews published by Cochrane Consumers and Communication. Evidence Bulletins are designed for health decision makers employed by or in representational roles within policy and practice settings, that is, policy makers, healt…
Perceived barriers and facilitators to participation in physical activity for children with disability
Online health information seeking
BACKGROUND AND OBJECTIVE: The Internet is increasingly prominent as a source of health information for people with multiple sclerosis (MS). But there has been little exploration of the needs, experiences and preferences of people with MS for integrating treatment information into decision making, in the context of searching on the Internet. This was the aim of our study. DESIGN: Sixty participants (51 people with MS; nine family members) took par…
Comparing Face-to-Face and Online Qualitative Research With People With Multiple Sclerosis
We compared face-to-face focus groups and an online forum in qualitative research with people with multiple sclerosis (MS) and family members. Although the merits and challenges of online qualitative research have been considered by others, there is limited literature directly comparing these two data collection methods for people with disability or chronic illness. Twenty-seven people participated in one of four focus groups and 33 people took p…
Comparing Face-to-Face and Online Qualitative Research With People With Multiple Sclerosis
We compared face-to-face focus groups and an online forum in qualitative research with people with multiple sclerosis (MS) and family members. Although the merits and challenges of online qualitative research have been considered by others, there is limited literature directly comparing these two data collection methods for people with disability or chronic illness. Twenty-seven people participated in one of four focus groups and 33 people took p…
The evolution of Cochrane evidence summaries in health communication and participation
Knowledge translation resources that summarise and disseminate systematic review findings can support evidence into policy and practice. Since 2007, we have produced Evidence Bulletins; brief, web-based summaries of Cochrane Reviews published by Cochrane Consumers and Communication. Evidence Bulletins are designed for health decision makers employed by or in representational roles within policy and practice settings, that is, policy makers, healt…
Comparing Face-to-Face and Online Qualitative Research With People With Multiple Sclerosis
We compared face-to-face focus groups and an online forum in qualitative research with people with multiple sclerosis (MS) and family members. Although the merits and challenges of online qualitative research have been considered by others, there is limited literature directly comparing these two data collection methods for people with disability or chronic illness. Twenty-seven people participated in one of four focus groups and 33 people took p…
Perceived barriers and facilitators to participation in physical activity for children with disability
Online health information seeking
BACKGROUND AND OBJECTIVE: The Internet is increasingly prominent as a source of health information for people with multiple sclerosis (MS). But there has been little exploration of the needs, experiences and preferences of people with MS for integrating treatment information into decision making, in the context of searching on the Internet. This was the aim of our study. DESIGN: Sixty participants (51 people with MS; nine family members) took par…
The evolution of Cochrane evidence summaries in health communication and participation
Knowledge translation resources that summarise and disseminate systematic review findings can support evidence into policy and practice. Since 2007, we have produced Evidence Bulletins; brief, web-based summaries of Cochrane Reviews published by Cochrane Consumers and Communication. Evidence Bulletins are designed for health decision makers employed by or in representational roles within policy and practice settings, that is, policy makers, healt…
Health-related quality of life after traumatic brain injury
By transforming the QOLIBRI-OS into utility scores, we enabled the application in economic evaluations and in summary measures of population health, which may be used to inform decision-makers on the best interventions and strategies for TBI patients
Stakeholder Involvement in Systematic Reviews
Case study 1 describes stakeholder involvement in setting systematic review priorities
Medicine (4 obras) · Psychology (4 obras) · Computer Science (3 obras) · Gerontology (3 obras) · Sociology (3 obras) · Focus group (2 obras) · Health care (2 obras) · Health Policy Implementation Science (2 obras) · Healthcare Systems and Technology (2 obras) · Medical education (2 obras)