Jos M Latour
Biographic Data
| ID | 3433798 |
|---|---|
| NAME | Jos M Latour |
| GIVEN NAMES | Jos M |
| FAMILY NAME | Latour |
| SIGNATURE | LATOUR J M |
| AFFILIATIONS | University of Plymouth |
| ORCID | 0000-0002-8087-6461 |
| VERIFIED | Yes |
| TOTAL WORKS | 12 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 12 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2009 |
| LATEST PUBLICATION YEAR | 2026 |
| H-INDEX | 0 |
Parents' Experiences and Reported Outcomes of Family‐Centred Care
Introduction Having an infant admitted to neonatal intensive care units (NICUs) is a distressing experience for parents. Family‐centred care (FCC) has been shown to improve outcomes for both infants and parents. However, there is inconsistency in reporting outcomes in FCC studies. The aim of this qualitative systematic review is to synthesise the experiences of parents related to FCC and to identify outcomes derived from these experiences to info…
Exploring the Views of Children With Cerebral Palsy, Their Parents and Physiotherapists on Participating in a Feasibility Randomised Controlled Trial Testing an Exergaming Device
BACKGROUND: This study aimed to understand the experiences and views of children with cerebral palsy, their parents and physiotherapists participating in the ACCEPT feasibility randomised controlled trial, which explored a 10-week physiotherapy intervention using an interactive gaming training device. DESIGN: Qualitative methods included semi-structured interviews, e-diary and photographs. Nine parent-child dyads and three physiotherapists partic…
Exploring Patient, Parent and Clinician Views of Outcomes for Family-Centered Care in Neonatal Settings
Participants' experiences provide meaningful insights into outcomes that should be evaluated in neonatal research and practice. These findings will inform the development of a COS for FCC in neonatal settings
A Closer Look at Parental Narratives
Background/Objectives: Bronchopulmonary dysplasia (BPD) is a chronic lung disease affecting preterm infants, often resulting in prolonged neonatal intensive care unit (NICU) stays and significant parental stress. The experiences of parents navigating their preterm infant's early NICU journey are important to support clinical trials to improve infant outcomes. Aim: The aim of this study was to explore parental perceptions of their infant's health …
Physical, Cognitive, Emotional, and Social Health Outcomes of Parents in the First Six Months after Childhood Critical Illness
Childhood critical illness can have long-term effects on families, but the extent and trajectory of recovery for parents are unknown. Using prospective longitudinal design, we describe the health outcomes of parents and their trajectory six months after paediatric intensive care unit (PICU) discharge. Parents reported health outcomes at PICU discharge (baseline), and 1-, 3-, and 6-months post-discharge. We used the Pediatric Quality-of-Life Famil…
Covid-19 and pregnancy
This study provides valuable insights into the impact of pregnancy and pre-existing comorbidities on COVID-19 outcomes in WRA. The findings underscore the importance of considering demographic factors and pre-existing comorbidities in the management of PW with COVID-19. The study also highlights the need for further research to understand the unique impacts of different comorbidities, particularly immunosuppression and renal disease, on COVID-19 …
Involving patients and caregivers to develop items for a new patient‐reported experience measure for older adults attending the emergency department. Findings from a nominal group technique study
Staff Perceptions of Family-Centered Care in Italian Neonatal Intensive Care Units
Family Centered Care (FCC) in Neonatal Intensive Care Units (NICUs) included family involvement in the care process of newborns and infants. Staff perceptions of FCC may influence clinical practice and management strategies in NICUs, with an impact on quality and humanization of the care. The Family-Centred Care Questionnaire-Revised (FCCQ-R) was adapted for the NICU setting, therefore the FCCQ-R@it-NICU was developed and used for the present stu…
Stress, Burnout, and Coping Strategies of Frontline Nurses During the Covid-19 Epidemic in Wuhan and Shanghai, China
Background: Nurses at the frontline of caring for COVID-19 patients might experience mental health challenges and supportive coping strategies are needed to reduce their stress and burnout. The aim of this study was to identify stressors and burnout among frontline nurses caring for COVID-19 patients in Wuhan and Shanghai and to explore perceived effective morale support strategies. Method: A cross-sectional survey was conducted in March 2020 amo…
Measuring parents’ perspective on continuity of care in children with special health care needs
SpeNK-Q proved to be a psychometrically promising instrument. Its utilisation could improve the identification of areas for service development, the delivery of coordinated care and support policy makers in redesigning integrated services
Exciting but exhausting
Background Adolescents with chronic conditions are major users of paediatric hospitals, but seldom participate in the evaluation of services or in research. Little is known about the usefulness of the participatory approach in adolescent health research. Objective To evaluate the feasibility, benefits and limitations of a participatory research (PR) project involving chronically ill adolescents as co‐researchers. Design, setting and participants …
Bridging the gap between paediatric to adult care
INTRODUCTION: Despite growing numbers of adolescents with chronic conditions, transition from paediatric to adult care has received little attention in the Netherlands. AIM: To identify gaps in transition to adult care of chronically ill adolescents from the perspectives of youth, parents and caregivers. METHODS: Semi-structured interviews with 24 adolescents (aged 15–22, with various chronic conditions), 24 parents and 17 healthcare professional…
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Bridging the gap between paediatric to adult care
INTRODUCTION: Despite growing numbers of adolescents with chronic conditions, transition from paediatric to adult care has received little attention in the Netherlands. AIM: To identify gaps in transition to adult care of chronically ill adolescents from the perspectives of youth, parents and caregivers. METHODS: Semi-structured interviews with 24 adolescents (aged 15–22, with various chronic conditions), 24 parents and 17 healthcare professional…
Exciting but exhausting
Background Adolescents with chronic conditions are major users of paediatric hospitals, but seldom participate in the evaluation of services or in research. Little is known about the usefulness of the participatory approach in adolescent health research. Objective To evaluate the feasibility, benefits and limitations of a participatory research (PR) project involving chronically ill adolescents as co‐researchers. Design, setting and participants …
Measuring parents’ perspective on continuity of care in children with special health care needs
SpeNK-Q proved to be a psychometrically promising instrument. Its utilisation could improve the identification of areas for service development, the delivery of coordinated care and support policy makers in redesigning integrated services
Stress, Burnout, and Coping Strategies of Frontline Nurses During the Covid-19 Epidemic in Wuhan and Shanghai, China
Background: Nurses at the frontline of caring for COVID-19 patients might experience mental health challenges and supportive coping strategies are needed to reduce their stress and burnout. The aim of this study was to identify stressors and burnout among frontline nurses caring for COVID-19 patients in Wuhan and Shanghai and to explore perceived effective morale support strategies. Method: A cross-sectional survey was conducted in March 2020 amo…
Staff Perceptions of Family-Centered Care in Italian Neonatal Intensive Care Units
Family Centered Care (FCC) in Neonatal Intensive Care Units (NICUs) included family involvement in the care process of newborns and infants. Staff perceptions of FCC may influence clinical practice and management strategies in NICUs, with an impact on quality and humanization of the care. The Family-Centred Care Questionnaire-Revised (FCCQ-R) was adapted for the NICU setting, therefore the FCCQ-R@it-NICU was developed and used for the present stu…
Involving patients and caregivers to develop items for a new patient‐reported experience measure for older adults attending the emergency department. Findings from a nominal group technique study
Physical, Cognitive, Emotional, and Social Health Outcomes of Parents in the First Six Months after Childhood Critical Illness
Childhood critical illness can have long-term effects on families, but the extent and trajectory of recovery for parents are unknown. Using prospective longitudinal design, we describe the health outcomes of parents and their trajectory six months after paediatric intensive care unit (PICU) discharge. Parents reported health outcomes at PICU discharge (baseline), and 1-, 3-, and 6-months post-discharge. We used the Pediatric Quality-of-Life Famil…
Covid-19 and pregnancy
This study provides valuable insights into the impact of pregnancy and pre-existing comorbidities on COVID-19 outcomes in WRA. The findings underscore the importance of considering demographic factors and pre-existing comorbidities in the management of PW with COVID-19. The study also highlights the need for further research to understand the unique impacts of different comorbidities, particularly immunosuppression and renal disease, on COVID-19 …
A Closer Look at Parental Narratives
Background/Objectives: Bronchopulmonary dysplasia (BPD) is a chronic lung disease affecting preterm infants, often resulting in prolonged neonatal intensive care unit (NICU) stays and significant parental stress. The experiences of parents navigating their preterm infant's early NICU journey are important to support clinical trials to improve infant outcomes. Aim: The aim of this study was to explore parental perceptions of their infant's health …
Parents' Experiences and Reported Outcomes of Family‐Centred Care
Introduction Having an infant admitted to neonatal intensive care units (NICUs) is a distressing experience for parents. Family‐centred care (FCC) has been shown to improve outcomes for both infants and parents. However, there is inconsistency in reporting outcomes in FCC studies. The aim of this qualitative systematic review is to synthesise the experiences of parents related to FCC and to identify outcomes derived from these experiences to info…
Exploring the Views of Children With Cerebral Palsy, Their Parents and Physiotherapists on Participating in a Feasibility Randomised Controlled Trial Testing an Exergaming Device
BACKGROUND: This study aimed to understand the experiences and views of children with cerebral palsy, their parents and physiotherapists participating in the ACCEPT feasibility randomised controlled trial, which explored a 10-week physiotherapy intervention using an interactive gaming training device. DESIGN: Qualitative methods included semi-structured interviews, e-diary and photographs. Nine parent-child dyads and three physiotherapists partic…
Exploring Patient, Parent and Clinician Views of Outcomes for Family-Centered Care in Neonatal Settings
Participants' experiences provide meaningful insights into outcomes that should be evaluated in neonatal research and practice. These findings will inform the development of a COS for FCC in neonatal settings
Medicine (9 works) · Psychology (8 works) · Infant Development and Preterm Care (5 works) · Nursing (5 works) · Health care (4 works) · Neonatal Respiratory Health Research (4 works) · Psychiatry (4 works) · Qualitative research (4 works) · Childhood Cancer Survivors' Quality of Life (3 works) · Clinical Psychology (3 works)