Melanie Calvert
Datos Biográficos
| ID | 2364672 |
|---|---|
| NOMBRE | Melanie Calvert |
| NOMBRES | Melanie |
| APELLIDO | Calvert |
| FIRMA | CALVERT M |
| AFILIACIONES | University of Birmingham |
| ORCID | 0000-0002-1856-837X |
| VERIFICADO | Sí |
| TOTAL DE OBRAS | 19 |
| TOTAL DE CITAS | 12 |
| TOTAL COMO AUTOR | 19 |
| TOTAL COMO EDITOR | 0 |
| PRIMER AÑO DE PUBLICACIÓN | 2011 |
| AÑO MÁS RECIENTE DE PUBLICACIÓN | 2025 |
| ÍNDICE H | 2 |
Health-related quality of life and economic impacts in adults with transfusion-dependent β-thalassemia
Participants reported substantial humanistic and economic burdens associated with living with TDT. Our findings highlight the need for alternative treatment options that contribute to improvements in HRQoL and reduce economic burden in this patient population
Cosmin reporting guideline for studies on measurement properties of patient‐reported outcome measures
Health-related quality of life and economic impacts in adults with sickle cell disease with recurrent vaso-occlusive crises
Participants reported significant impairments to their HRQoL and financial constraints associated with SCD with recurrent VOCs, indicating humanistic and economic burden and unmet needs in this population
Electronic outcome assessments in integrated care
Do electronic outcome assessments offer an opportunity to bolster the effectiveness of integrated care in settings where individuals may receive both healthcare and social services? Integrated Care Systems (ICS) were formed to create partnerships involving the National Health Service, local councils, community and voluntary organisations, local residents, people who use services and their carers with a role in supporting the health and wellbeing …
Self-reported outcomes within integrated care – a bridge between health and social care
Self-report questionnaires can enable health and social care organisations to understand better a person’s views about their health and well-being, allowing them to provide effective, safe, individualised integrated care. Outcomes are the results from care and/or treatments people have received whilst in clinical or other care settings. Some outcomes, such as symptoms, quality of life and aspects of physical, mental, and social functioning can on…
Patient-Reported Outcomes in Integrated Care
Effective care integration requires the right information, at the right time, with care and support delivered in the right environment. Patient-reported outcome measures [PROMs] offer a mechanism to support collaborative integrated care to help people understand their conditions better, live well, and remain independent. Through the lens of the delivery of integrated care in England, we consider the opportunities and challenges associated with th…
Directrices para presentación de informes de ensayos clínicos sobre intervenciones con inteligencia artificial
La declaración CONSORT 2010 proporciona unas directrices mínimas para informar sobre los ensayos clínicos aleatorizados. Su uso generalizado ha sido fundamental para garantizar la transparencia en la evaluación de nuevas intervenciones. Más recientemente, se ha reconocido cada vez más que las intervenciones con inteligencia artificial (IA) deben someterse a una evaluación rigurosa y prospectiva para demostrar su impacto en la salud. La extensión …
Directrices para los protocolos de ensayos clínicos de intervenciones con inteligencia artificial
La declaración SPIRIT 2013 tiene como objetivo mejorar la exhaustividad de los informes de los protocolos de los ensayos clínicos proporcionando recomendaciones basadas en la evidencia para el conjunto mínimo de elementos que deben abordarse. Esta guía ha sido fundamental para promover la evaluación transparente de nuevas intervenciones. Más recientemente, se ha reconocido cada vez más que las intervenciones con inteligencia artificial (IA) deben…
Symptoms and risk factors for long Covid in non-hospitalized adults
Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection is associated with a range of persistent symptoms impacting everyday functioning, known as post-COVID-19 condition or long COVID. We undertook a retrospective matched cohort study using a UK-based primary care database, Clinical Practice Research Datalink Aurum, to determine symptoms that are associated with confirmed SARS-CoV-2 infection beyond 12 weeks in non-hospitalized ad…
A Literature Review of Studies that Have Compared the Use of Face-To-Face and Online Focus Groups
Online communication in our work and private lives has increased significantly since the COVID-19 pandemic. Qualitative research has evolved with this trend with many studies adopting online methods. It is therefore timely to assess the use and utility of online focus groups compared to face-to-face focus groups. Traditional Pearl Growing Methodology was used to identify eligible papers. Data were extracted on data collection methods, recruitment…
Symptoms, complications and management of long Covid
Globally, there are now over 160 million confirmed cases of COVID-19 and more than 3 million deaths. While the majority of infected individuals recover, a significant proportion continue to experience symptoms and complications after their acute illness. Patients with ‘long COVID’ experience a wide range of physical and mental/psychological symptoms. Pooled prevalence data showed the 10 most prevalent reported symptoms were fatigue, shortness of …
What to expect after open heart valve surgery? Changes in health-related quality of life
Six mechanisms behind carer wellbeing effects
Preliminary evidence on the uptake, use and benefits of the Consort-PRO extension
International Society for Quality of Life Research commentary on the draft European Medicines Agency reflection paper on the use of patient-reported outcome (PRO) measures in oncology studies
Integrating health-related quality of life findings from randomized clinical trials into practice
Clinical Use of Health-Related Quality of Life Outcomes From Cancer Clinical Trials
Introduction There have been increasing efforts aimed at enhancing patient-centered care and incorporating patients' voice into clinical practice. As such, a growing body of literature has recognized the importance of Health-Related Quality of Life (HRQOL) outcomes from clinical trials. HRQOL outcomes are often collected in Phase III randomized controlled trials (RCTs), along with survival data, morbidity, and toxicity data. HRQOL outcomes are me…
Health-related quality of life and supportive care in patients with rare long-term neurological conditions
Reaching the ‘hard to reach’
Little is known about health and social care experiences of patients with rare long-term neurological conditions. Furthermore, black and minority ethnic (BME) service users are often perceived to be under-represented in health services research. BME service users have been described as ‘hard to reach’ in the past. However, evidence suggests that a variety of recruitment methods need to be used in order to increase recruitment. We employed a range…
Reaching the ‘hard to reach’
Little is known about health and social care experiences of patients with rare long-term neurological conditions. Furthermore, black and minority ethnic (BME) service users are often perceived to be under-represented in health services research. BME service users have been described as ‘hard to reach’ in the past. However, evidence suggests that a variety of recruitment methods need to be used in order to increase recruitment. We employed a range…
Six mechanisms behind carer wellbeing effects
Reaching the ‘hard to reach’
Little is known about health and social care experiences of patients with rare long-term neurological conditions. Furthermore, black and minority ethnic (BME) service users are often perceived to be under-represented in health services research. BME service users have been described as ‘hard to reach’ in the past. However, evidence suggests that a variety of recruitment methods need to be used in order to increase recruitment. We employed a range…
Health-related quality of life and supportive care in patients with rare long-term neurological conditions
Clinical Use of Health-Related Quality of Life Outcomes From Cancer Clinical Trials
Introduction There have been increasing efforts aimed at enhancing patient-centered care and incorporating patients' voice into clinical practice. As such, a growing body of literature has recognized the importance of Health-Related Quality of Life (HRQOL) outcomes from clinical trials. HRQOL outcomes are often collected in Phase III randomized controlled trials (RCTs), along with survival data, morbidity, and toxicity data. HRQOL outcomes are me…
Integrating health-related quality of life findings from randomized clinical trials into practice
International Society for Quality of Life Research commentary on the draft European Medicines Agency reflection paper on the use of patient-reported outcome (PRO) measures in oncology studies
Preliminary evidence on the uptake, use and benefits of the Consort-PRO extension
What to expect after open heart valve surgery? Changes in health-related quality of life
Six mechanisms behind carer wellbeing effects
Symptoms, complications and management of long Covid
Globally, there are now over 160 million confirmed cases of COVID-19 and more than 3 million deaths. While the majority of infected individuals recover, a significant proportion continue to experience symptoms and complications after their acute illness. Patients with ‘long COVID’ experience a wide range of physical and mental/psychological symptoms. Pooled prevalence data showed the 10 most prevalent reported symptoms were fatigue, shortness of …
Symptoms and risk factors for long Covid in non-hospitalized adults
Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection is associated with a range of persistent symptoms impacting everyday functioning, known as post-COVID-19 condition or long COVID. We undertook a retrospective matched cohort study using a UK-based primary care database, Clinical Practice Research Datalink Aurum, to determine symptoms that are associated with confirmed SARS-CoV-2 infection beyond 12 weeks in non-hospitalized ad…
A Literature Review of Studies that Have Compared the Use of Face-To-Face and Online Focus Groups
Online communication in our work and private lives has increased significantly since the COVID-19 pandemic. Qualitative research has evolved with this trend with many studies adopting online methods. It is therefore timely to assess the use and utility of online focus groups compared to face-to-face focus groups. Traditional Pearl Growing Methodology was used to identify eligible papers. Data were extracted on data collection methods, recruitment…
Directrices para presentación de informes de ensayos clínicos sobre intervenciones con inteligencia artificial
La declaración CONSORT 2010 proporciona unas directrices mínimas para informar sobre los ensayos clínicos aleatorizados. Su uso generalizado ha sido fundamental para garantizar la transparencia en la evaluación de nuevas intervenciones. Más recientemente, se ha reconocido cada vez más que las intervenciones con inteligencia artificial (IA) deben someterse a una evaluación rigurosa y prospectiva para demostrar su impacto en la salud. La extensión …
Directrices para los protocolos de ensayos clínicos de intervenciones con inteligencia artificial
La declaración SPIRIT 2013 tiene como objetivo mejorar la exhaustividad de los informes de los protocolos de los ensayos clínicos proporcionando recomendaciones basadas en la evidencia para el conjunto mínimo de elementos que deben abordarse. Esta guía ha sido fundamental para promover la evaluación transparente de nuevas intervenciones. Más recientemente, se ha reconocido cada vez más que las intervenciones con inteligencia artificial (IA) deben…
Health-related quality of life and economic impacts in adults with transfusion-dependent β-thalassemia
Participants reported substantial humanistic and economic burdens associated with living with TDT. Our findings highlight the need for alternative treatment options that contribute to improvements in HRQoL and reduce economic burden in this patient population
Cosmin reporting guideline for studies on measurement properties of patient‐reported outcome measures
Health-related quality of life and economic impacts in adults with sickle cell disease with recurrent vaso-occlusive crises
Participants reported significant impairments to their HRQoL and financial constraints associated with SCD with recurrent VOCs, indicating humanistic and economic burden and unmet needs in this population
Electronic outcome assessments in integrated care
Do electronic outcome assessments offer an opportunity to bolster the effectiveness of integrated care in settings where individuals may receive both healthcare and social services? Integrated Care Systems (ICS) were formed to create partnerships involving the National Health Service, local councils, community and voluntary organisations, local residents, people who use services and their carers with a role in supporting the health and wellbeing …
Self-reported outcomes within integrated care – a bridge between health and social care
Self-report questionnaires can enable health and social care organisations to understand better a person’s views about their health and well-being, allowing them to provide effective, safe, individualised integrated care. Outcomes are the results from care and/or treatments people have received whilst in clinical or other care settings. Some outcomes, such as symptoms, quality of life and aspects of physical, mental, and social functioning can on…
Patient-Reported Outcomes in Integrated Care
Effective care integration requires the right information, at the right time, with care and support delivered in the right environment. Patient-reported outcome measures [PROMs] offer a mechanism to support collaborative integrated care to help people understand their conditions better, live well, and remain independent. Through the lens of the delivery of integrated care in England, we consider the opportunities and challenges associated with th…
Medicine (17 obras) · Nursing (10 obras) · Psychology (9 obras) · Internal Medicine (8 obras) · Health Systems, Economic Evaluations, Quality of Life (7 obras) · Gerontology (6 obras) · Quality of life (healthcare (6 obras) · Computer Science (5 obras) · Family medicine (5 obras) · Pathology (5 obras)