Julien Mancini
Dados Biográficos
| ID | 4567920 |
|---|---|
| NOME | Julien Mancini |
| PRENOMES | Julien |
| SOBRENOME | Mancini |
| ASSINATURA | MANCINI J |
| AFILIAÇÕES | Julien Mancini, Marie-Claude Simeoni, Audrey Clément, and Pascal Auquier are with the Self-Perceived Health Assessment Research Unit (EA3279), Mediterranée University School of Medicine, Marseille, France. Patrice Viens is with the Department of Medical Oncology, Paoli-Calmettes Institute, Marseille. |
| VERIFICADO | Não |
| TOTAL DE OBRAS | 7 |
| TOTAL DE CITAÇÕES | 4 |
| TOTAL COMO AUTOR | 7 |
| TOTAL COMO EDITOR | 0 |
| PRIMEIRO ANO DE PUBLICAÇÃO | 2006 |
| ANO MAIS RECENTE DE PUBLICAÇÃO | 2025 |
| ÍNDICE H | 2 |
Measuring digital health literacy and its associations with determinants and health outcomes in 13 countries
Introduction: Digital health information sources are playing an increasingly prominent role in health promotion, public health and in healthcare systems. Consequently, digital health literacy skills are likewise becoming increasingly important. Methods: -DIGI, applied in the European Health Literacy Survey (2019-2021) of the WHO M-POHL network, analyzing data from 28,057 respondents from 13 countries. The instrument is a modified and extended ver…
Medical Cannabis
International audience
Disclosure of research results
BACKGROUND: There exist no recommendations as to how aggregate research results should best be disclosed to long-term cohort participants. OBJECTIVE: To study the impact of cohort results disclosure documents of various kinds on participants' satisfaction. DESIGN: Randomized study with a 2x2 factorial design. SETTING AND PARTICIPANTS: The GENEPSO-PS cohort is used to study the psychosocial characteristics and preventive behaviour of both BRCA1/2 …
Contributing to research via biobanks
Context and objective Biobanks have become strategic resources for biomedical and genetic research. The aim of the present empirical qualitative study was to investigate how patients with cancer perceive and experience the process of donation to biobanks, focussing on the subjective meanings associated with their decisions when they are asked in a routine context to agree to their own biological specimens being used for research projects. Design …
They should take time
Cross-cultural validation of the Decisional Conflict Scale in a sample of French patients
A Modest Impact of Cancer on Young Adult Caregivers’ Educational Plans
In the November 2005 issue of the Journal, Levine et al.1 underlined the need for qualitative studies to elucidate the impact of caregiving on young adults (aged 18 to 25 years) who become natural caregivers for family members or friends. They also asked for additional specific research on the impact of caregiving on the educational plans of these young caregivers. As part of a larger study on the impact of cancer in a sample that included a broa…
They should take time
A Modest Impact of Cancer on Young Adult Caregivers’ Educational Plans
In the November 2005 issue of the Journal, Levine et al.1 underlined the need for qualitative studies to elucidate the impact of caregiving on young adults (aged 18 to 25 years) who become natural caregivers for family members or friends. They also asked for additional specific research on the impact of caregiving on the educational plans of these young caregivers. As part of a larger study on the impact of cancer in a sample that included a broa…
Cross-cultural validation of the Decisional Conflict Scale in a sample of French patients
A Modest Impact of Cancer on Young Adult Caregivers’ Educational Plans
In the November 2005 issue of the Journal, Levine et al.1 underlined the need for qualitative studies to elucidate the impact of caregiving on young adults (aged 18 to 25 years) who become natural caregivers for family members or friends. They also asked for additional specific research on the impact of caregiving on the educational plans of these young caregivers. As part of a larger study on the impact of cancer in a sample that included a broa…
They should take time
Contributing to research via biobanks
Context and objective Biobanks have become strategic resources for biomedical and genetic research. The aim of the present empirical qualitative study was to investigate how patients with cancer perceive and experience the process of donation to biobanks, focussing on the subjective meanings associated with their decisions when they are asked in a routine context to agree to their own biological specimens being used for research projects. Design …
Disclosure of research results
BACKGROUND: There exist no recommendations as to how aggregate research results should best be disclosed to long-term cohort participants. OBJECTIVE: To study the impact of cohort results disclosure documents of various kinds on participants' satisfaction. DESIGN: Randomized study with a 2x2 factorial design. SETTING AND PARTICIPANTS: The GENEPSO-PS cohort is used to study the psychosocial characteristics and preventive behaviour of both BRCA1/2 …
Medical Cannabis
International audience
Measuring digital health literacy and its associations with determinants and health outcomes in 13 countries
Introduction: Digital health information sources are playing an increasingly prominent role in health promotion, public health and in healthcare systems. Consequently, digital health literacy skills are likewise becoming increasingly important. Methods: -DIGI, applied in the European Health Literacy Survey (2019-2021) of the WHO M-POHL network, analyzing data from 28,057 respondents from 13 countries. The instrument is a modified and extended ver…
Medicine (6 obras) · Psychology (5 obras) · Ethics in Clinical Research (3 obras) · Nursing (3 obras) · Patient-Provider Communication in Healthcare (3 obras) · Political science (3 obras) · Psychiatry (3 obras) · Social Psychology (3 obras) · Sociology (3 obras) · BRCA gene mutations in cancer (2 obras)