Yvonne C Learmonth
Dados Biográficos
| ID | 4265671 |
|---|---|
| NOME | Yvonne C Learmonth |
| PRENOMES | Yvonne C |
| SOBRENOME | Learmonth |
| ASSINATURA | LEARMONTH Y C |
| AFILIAÇÕES | University of Illinois Urbana-Champaign |
| ORCID | 0000-0002-4857-8480 |
| VERIFICADO | Sim |
| TOTAL DE OBRAS | 9 |
| TOTAL DE CITAÇÕES | 2 |
| TOTAL COMO AUTOR | 9 |
| TOTAL COMO EDITOR | 0 |
| PRIMEIRO ANO DE PUBLICAÇÃO | 2014 |
| ANO MAIS RECENTE DE PUBLICAÇÃO | 2026 |
| ÍNDICE H | 1 |
Assessing Unmet Social Needs in Multiple Sclerosis Care in Australia
BACKGROUND: Unmet social needs (including housing, transport and social inclusion) contribute substantially to health outcomes, especially for people with long-term health conditions such as multiple sclerosis (MS). Whether assessment of unmet social needs occurs in MS clinical care is unclear. This study aims to (1) understand current practices, (2) identify barriers and enablers to social needs assessments in MS care, and (3) explore the feasib…
Social Needs Screening Tools for Clinical Populations in Australia and New Zealand
BACKGROUND: Social determinants of health account for approximately 50% of health outcomes, yet social needs are rarely assessed as part of routine clinical care. We aimed to conduct a scoping review of screening tools for assessing social needs within clinical practice in Australia and New Zealand. METHODS: This scoping review was conducted according to our preregistered protocol (https://osf.io/d6evu). We searched scientific and grey literature…
Crisis preparation for people with multiple sclerosis in Australia
With increasing prevalence of disasters or crises such as fires, floods, and pandemics globally, people with disabilities are disproportionally at risk for short- and long-term consequences. We surveyed 1479 people with multiple sclerosis (MS) living in Australia to understand their needs for a crisis preparation plan. Only 17.4% already had a plan that met their needs, 31.0% and 6.5% indicated they would find creating or updating a plan helpful …
Exploring Covid‐19 experiences for persons with multiple sclerosis and carers
OBJECTIVE: The COVID-19 pandemic continues to impact communities around the world. In this study, we explored the COVID-19 experiences of persons with multiple sclerosis (MS) and carers. METHODS: Using a qualitative approach, interviews were undertaken with 27 participants residing in Australia (10 persons with MS, 10 carers and 7 MS service providers). Demographic and background data were also collected. Interviews were analysed using an inducti…
Feasibility Meets Implementation Science
Background There is a need to identify why multiple sclerosis exercise research is not translating into real-world participation. To lay the foundations of strong clinical research, considering the translational element of implementation science at the feasibility phase of a trial is vital. Methods Document analysis was used to examine document sources on exercise activity interventions designed for people living with multiple sclerosis. Document…
Identifying preferred format and source of exercise information in persons with multiple sclerosis that can be delivered by health‐care providers
BACKGROUND: There is increasing recognition of the benefits of exercise in individuals with multiple sclerosis (MS), yet the MS population does not engage in sufficient amounts of exercise to accrue health benefits. There has been little qualitative inquiry to establish the preferred format and source for receiving exercise information from health-care providers among persons with MS. OBJECTIVE: We sought to identify the desired and preferred for…
Multiple sclerosis patients need and want information on exercise promotion from healthcare providers
BACKGROUND: There is growing recognition of the benefits and safety of exercise and its importance in the comprehensive care of persons with multiple sclerosis (MS), yet uptake is low. OBJECTIVE: We explored the needs and wants of patients with MS regarding exercise promotion through healthcare providers. SETTING AND PARTICIPANTS: Participants were adults with MS who had mild-or-moderate disability and a range of exercise levels. All participants…
Quality of Life and Health-Related Quality of Life over 1 Year in Older Women
Psychometric properties of quality of life and health-related quality of life assessments in people with multiple sclerosis
Feasibility Meets Implementation Science
Background There is a need to identify why multiple sclerosis exercise research is not translating into real-world participation. To lay the foundations of strong clinical research, considering the translational element of implementation science at the feasibility phase of a trial is vital. Methods Document analysis was used to examine document sources on exercise activity interventions designed for people living with multiple sclerosis. Document…
Quality of Life and Health-Related Quality of Life over 1 Year in Older Women
Psychometric properties of quality of life and health-related quality of life assessments in people with multiple sclerosis
Quality of Life and Health-Related Quality of Life over 1 Year in Older Women
Identifying preferred format and source of exercise information in persons with multiple sclerosis that can be delivered by health‐care providers
BACKGROUND: There is increasing recognition of the benefits of exercise in individuals with multiple sclerosis (MS), yet the MS population does not engage in sufficient amounts of exercise to accrue health benefits. There has been little qualitative inquiry to establish the preferred format and source for receiving exercise information from health-care providers among persons with MS. OBJECTIVE: We sought to identify the desired and preferred for…
Multiple sclerosis patients need and want information on exercise promotion from healthcare providers
BACKGROUND: There is growing recognition of the benefits and safety of exercise and its importance in the comprehensive care of persons with multiple sclerosis (MS), yet uptake is low. OBJECTIVE: We explored the needs and wants of patients with MS regarding exercise promotion through healthcare providers. SETTING AND PARTICIPANTS: Participants were adults with MS who had mild-or-moderate disability and a range of exercise levels. All participants…
Exploring Covid‐19 experiences for persons with multiple sclerosis and carers
OBJECTIVE: The COVID-19 pandemic continues to impact communities around the world. In this study, we explored the COVID-19 experiences of persons with multiple sclerosis (MS) and carers. METHODS: Using a qualitative approach, interviews were undertaken with 27 participants residing in Australia (10 persons with MS, 10 carers and 7 MS service providers). Demographic and background data were also collected. Interviews were analysed using an inducti…
Feasibility Meets Implementation Science
Background There is a need to identify why multiple sclerosis exercise research is not translating into real-world participation. To lay the foundations of strong clinical research, considering the translational element of implementation science at the feasibility phase of a trial is vital. Methods Document analysis was used to examine document sources on exercise activity interventions designed for people living with multiple sclerosis. Document…
Crisis preparation for people with multiple sclerosis in Australia
With increasing prevalence of disasters or crises such as fires, floods, and pandemics globally, people with disabilities are disproportionally at risk for short- and long-term consequences. We surveyed 1479 people with multiple sclerosis (MS) living in Australia to understand their needs for a crisis preparation plan. Only 17.4% already had a plan that met their needs, 31.0% and 6.5% indicated they would find creating or updating a plan helpful …
Assessing Unmet Social Needs in Multiple Sclerosis Care in Australia
BACKGROUND: Unmet social needs (including housing, transport and social inclusion) contribute substantially to health outcomes, especially for people with long-term health conditions such as multiple sclerosis (MS). Whether assessment of unmet social needs occurs in MS clinical care is unclear. This study aims to (1) understand current practices, (2) identify barriers and enablers to social needs assessments in MS care, and (3) explore the feasib…
Social Needs Screening Tools for Clinical Populations in Australia and New Zealand
BACKGROUND: Social determinants of health account for approximately 50% of health outcomes, yet social needs are rarely assessed as part of routine clinical care. We aimed to conduct a scoping review of screening tools for assessing social needs within clinical practice in Australia and New Zealand. METHODS: This scoping review was conducted according to our preregistered protocol (https://osf.io/d6evu). We searched scientific and grey literature…
Medicine (7 obras) · Health care (5 obras) · Multiple Sclerosis Research Studies (5 obras) · Nursing (5 obras) · Public health (5 obras) · Qualitative research (5 obras) · Disease (4 obras) · Psychology (4 obras) · Thematic analysis (4 obras) · Clinical Psychology (3 obras)