Kate Seers
Datos Biográficos
| ID | 259957 |
|---|---|
| NOMBRE | Kate Seers |
| NOMBRES | Kate |
| APELLIDO | Seers |
| FIRMA | SEERS K |
| AFILIACIONES | University of Warwick |
| ORCID | 0000-0001-7921-552X |
| VERIFICADO | Sí |
| TOTAL DE OBRAS | 9 |
| TOTAL DE CITAS | 10 |
| TOTAL COMO AUTOR | 9 |
| TOTAL COMO EDITOR | 0 |
| PRIMER AÑO DE PUBLICACIÓN | 2008 |
| AÑO MÁS RECIENTE DE PUBLICACIÓN | 2025 |
| ÍNDICE H | 2 |
Comparing In-Person and Remote Qualitative Data Collection Methods for Data Quality and Inclusion
Background: In-person data collection has long been considered the ‘gold standard’ for qualitative data collection. Societal changes and the rapid increase in the use of remote methods during the Covid-19 pandemic intensified debate about the limitations and opportunities of remote data collection, while reigniting questions about data quality and inclusion. Objective: We sought to map available evidence exploring the characteristics and quality …
A qualitative exploration into diagnostic barriers of gender-diverse autistic individuals
Research investigating gender disparities between autistic individuals has been restricted to a binary scope, focusing on how and why females are often overlooked within the diagnostic process. While this research has provided valuable insight, it neglects gender-diverse youth, limiting the understanding of why there are higher rates of autistic youth identifying as gender diverse compared to neurotypical children. A potential explanation for thi…
Fake it ‘till you make it”
The diagnosis of autism spectrum condition (ASC) in women is increasing, prompting research into the gendered experience and presentation of female ASC. To complement this growing body of research, the current study utilised a qualitative approach informed by a feminist disability framework to explore how the intersecting dimensions of difference, gender, and ASC influence autistic women’s subjectivity and wellbeing. Drawing on the experiences of…
GRIPP2 reporting checklists
While the patient and public involvement (PPI) evidence base has expanded over the past decade, the quality of reporting within papers is often inconsistent, limiting our understanding of how it works, in what context, for whom, and why. To develop international consensus on the key items to report to enhance the quality, transparency, and consistency of the PPI evidence base. To collaboratively involve patients as research partners at all stages…
GRIPP2 reporting checklists
Background While the patient and public involvement (PPI) evidence base has expanded over the past decade, the quality of reporting within papers is often inconsistent, limiting our understanding of how it works, in what context, for whom, and why. Objective To develop international consensus on the key items to report to enhance the quality, transparency, and consistency of the PPI evidence base. To collaboratively involve patients as research p…
The development of service user‐led recommendations for health and social care services on leaving hospital with memory loss or dementia – the SHARED study
BACKGROUND: Health and social care services are under strain providing care in the community particularly at hospital discharge. Patient and carer experiences can inform and shape services. OBJECTIVE: To develop service user-led recommendations enabling smooth transition for people living with memory loss from acute hospital to community. DESIGN: Lead and co-researchers conducted semi-structured interviews with 15 pairs of carers and patients wit…
Meta-ethnography 25 years on
Studies that systematically search for and synthesise qualitative research are becoming more evident in health care, and they can make an important contribution to patient care. Our team was funded to complete a meta-ethnography of patients' experience of chronic musculoskeletal pain. It has been 25 years since Noblit and Hare published their core text on meta-ethnography, and the current health research environment brings additional challenges t…
Somebody there to watch over you’
This paper reports on the role of family members in everyday diabetes self-care and in diabetic crises. It is based on qualitative data drawn from 45 semi-structured interviews with a wide range of people with an established diagnosis of Type 1 or Type 2 diabetes, who were admitted to hospital for urgent or emergency treatment in connection with their diabetes. The interviews were carried out in two contrasting sites in the United Kingdom in 2009…
Evaluating the successful implementation of evidence into practice using the PARiHS framework
BACKGROUND: The PARiHS framework (Promoting Action on Research Implementation in Health Services) has proved to be a useful practical and conceptual heuristic for many researchers and practitioners in framing their research or knowledge translation endeavours. However, as a conceptual framework it still remains untested and therefore its contribution to the overall development and testing of theory in the field of implementation science is largel…
Fake it ‘till you make it”
The diagnosis of autism spectrum condition (ASC) in women is increasing, prompting research into the gendered experience and presentation of female ASC. To complement this growing body of research, the current study utilised a qualitative approach informed by a feminist disability framework to explore how the intersecting dimensions of difference, gender, and ASC influence autistic women’s subjectivity and wellbeing. Drawing on the experiences of…
Somebody there to watch over you’
This paper reports on the role of family members in everyday diabetes self-care and in diabetic crises. It is based on qualitative data drawn from 45 semi-structured interviews with a wide range of people with an established diagnosis of Type 1 or Type 2 diabetes, who were admitted to hospital for urgent or emergency treatment in connection with their diabetes. The interviews were carried out in two contrasting sites in the United Kingdom in 2009…
A qualitative exploration into diagnostic barriers of gender-diverse autistic individuals
Research investigating gender disparities between autistic individuals has been restricted to a binary scope, focusing on how and why females are often overlooked within the diagnostic process. While this research has provided valuable insight, it neglects gender-diverse youth, limiting the understanding of why there are higher rates of autistic youth identifying as gender diverse compared to neurotypical children. A potential explanation for thi…
Evaluating the successful implementation of evidence into practice using the PARiHS framework
BACKGROUND: The PARiHS framework (Promoting Action on Research Implementation in Health Services) has proved to be a useful practical and conceptual heuristic for many researchers and practitioners in framing their research or knowledge translation endeavours. However, as a conceptual framework it still remains untested and therefore its contribution to the overall development and testing of theory in the field of implementation science is largel…
Somebody there to watch over you’
This paper reports on the role of family members in everyday diabetes self-care and in diabetic crises. It is based on qualitative data drawn from 45 semi-structured interviews with a wide range of people with an established diagnosis of Type 1 or Type 2 diabetes, who were admitted to hospital for urgent or emergency treatment in connection with their diabetes. The interviews were carried out in two contrasting sites in the United Kingdom in 2009…
Meta-ethnography 25 years on
Studies that systematically search for and synthesise qualitative research are becoming more evident in health care, and they can make an important contribution to patient care. Our team was funded to complete a meta-ethnography of patients' experience of chronic musculoskeletal pain. It has been 25 years since Noblit and Hare published their core text on meta-ethnography, and the current health research environment brings additional challenges t…
GRIPP2 reporting checklists
While the patient and public involvement (PPI) evidence base has expanded over the past decade, the quality of reporting within papers is often inconsistent, limiting our understanding of how it works, in what context, for whom, and why. To develop international consensus on the key items to report to enhance the quality, transparency, and consistency of the PPI evidence base. To collaboratively involve patients as research partners at all stages…
GRIPP2 reporting checklists
Background While the patient and public involvement (PPI) evidence base has expanded over the past decade, the quality of reporting within papers is often inconsistent, limiting our understanding of how it works, in what context, for whom, and why. Objective To develop international consensus on the key items to report to enhance the quality, transparency, and consistency of the PPI evidence base. To collaboratively involve patients as research p…
The development of service user‐led recommendations for health and social care services on leaving hospital with memory loss or dementia – the SHARED study
BACKGROUND: Health and social care services are under strain providing care in the community particularly at hospital discharge. Patient and carer experiences can inform and shape services. OBJECTIVE: To develop service user-led recommendations enabling smooth transition for people living with memory loss from acute hospital to community. DESIGN: Lead and co-researchers conducted semi-structured interviews with 15 pairs of carers and patients wit…
Fake it ‘till you make it”
The diagnosis of autism spectrum condition (ASC) in women is increasing, prompting research into the gendered experience and presentation of female ASC. To complement this growing body of research, the current study utilised a qualitative approach informed by a feminist disability framework to explore how the intersecting dimensions of difference, gender, and ASC influence autistic women’s subjectivity and wellbeing. Drawing on the experiences of…
Comparing In-Person and Remote Qualitative Data Collection Methods for Data Quality and Inclusion
Background: In-person data collection has long been considered the ‘gold standard’ for qualitative data collection. Societal changes and the rapid increase in the use of remote methods during the Covid-19 pandemic intensified debate about the limitations and opportunities of remote data collection, while reigniting questions about data quality and inclusion. Objective: We sought to map available evidence exploring the characteristics and quality …
A qualitative exploration into diagnostic barriers of gender-diverse autistic individuals
Research investigating gender disparities between autistic individuals has been restricted to a binary scope, focusing on how and why females are often overlooked within the diagnostic process. While this research has provided valuable insight, it neglects gender-diverse youth, limiting the understanding of why there are higher rates of autistic youth identifying as gender diverse compared to neurotypical children. A potential explanation for thi…
Psychology (7 obras) · Medicine (5 obras) · Sociology (5 obras) · Computer Science (4 obras) · Mental Health and Patient Involvement (4 obras) · Qualitative research (4 obras) · Business (3 obras) · Context (archaeology) (3 obras) · Focus group (3 obras) · Health Policy Implementation Science (3 obras)