Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Frances Shiely

Showing results (21-30 of 91) with videos related to

Pageof 10
Sort By:
Archives of Suicide Research : Official Journal of the International Academy for Suicide Research|June 25, 2020
Patients' Experiences of Engagement with Healthcare Services Following a High-Risk Self-Harm Presentation to a Hospital Emergency Department: A Mixed Methods StudyGrace Cully, Dorothy Leahy, Frances Shiely, et al.
Trials|February 7, 2023
Patient and Public Involvement (PPI) in outcome selection in breast cancer and nephrology trialsCiara Buckley, Shaun Treweek, Lynn Laidlaw, et al.
Journal of Clinical Epidemiology|September 21, 2025
Planning retention strategies in clinical trials-a qualitative interview study with members of trial teamsEllen Murphy, Sharon McCann, Frances Shiely, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|December 21, 2013
The prevalence of syphilis at childbirth in Ireland: a six-year reviewJennifer E Lutomski, Frances Shiely, Eleanor J Molloy
Trials|June 2, 2022
Tolerating bad health research: the continuing scandalStefania Pirosca, Frances Shiely, Mike Clarke, et al.
Trials|June 27, 2022
Getting it wrong most of the time? Comparing trialists' choice of primary outcome with what patients and health professionals wantShaun Treweek, Viviane Miyakoda, Dylan Burke, et al.
Trials|May 1, 2024
When describing harms and benefits to potential trial participants, participant information leaflets are inadequateLaura Cuddihy, Jeremy Howick, Ellen Murphy, et al.
Journal of Clinical Epidemiology|August 27, 2023
Underrecording and underreporting of participant ethnicity in clinical trials is persistent and is a threat to inclusivity and generalizabilityNeil Wallace, Stacey O'Keeffe, Heidi Gardner, et al.
Journal of Clinical Epidemiology|February 9, 2025
Lack of data collection in clinical trials prevents us from evaluating inclusion of people with disabilitiesShauna Cunningham, Amy M Russell, Emma Lidington, et al.
The Journal of Family Planning and Reproductive Health Care|June 12, 2014
Sexually transmitted infection incidence among adolescents in IrelandMartin P Davoren, Kevin Hayes, Mary Horgan, et al.
Pageof 10

Showing results (21-30 of 91) with videos related to

Sort By:
Pageof 10
Archives of Suicide Research : Official Journal of the International Academy for Suicide Research|June 25, 2020
Patients' Experiences of Engagement with Healthcare Services Following a High-Risk Self-Harm Presentation to a Hospital Emergency Department: A Mixed Methods StudyGrace Cully, Dorothy Leahy, Frances Shiely, et al.
Trials|February 7, 2023
Patient and Public Involvement (PPI) in outcome selection in breast cancer and nephrology trialsCiara Buckley, Shaun Treweek, Lynn Laidlaw, et al.
Journal of Clinical Epidemiology|September 21, 2025
Planning retention strategies in clinical trials-a qualitative interview study with members of trial teamsEllen Murphy, Sharon McCann, Frances Shiely, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|December 21, 2013
The prevalence of syphilis at childbirth in Ireland: a six-year reviewJennifer E Lutomski, Frances Shiely, Eleanor J Molloy
Trials|June 2, 2022
Tolerating bad health research: the continuing scandalStefania Pirosca, Frances Shiely, Mike Clarke, et al.
Trials|June 27, 2022
Getting it wrong most of the time? Comparing trialists' choice of primary outcome with what patients and health professionals wantShaun Treweek, Viviane Miyakoda, Dylan Burke, et al.
Trials|May 1, 2024
When describing harms and benefits to potential trial participants, participant information leaflets are inadequateLaura Cuddihy, Jeremy Howick, Ellen Murphy, et al.
Journal of Clinical Epidemiology|August 27, 2023
Underrecording and underreporting of participant ethnicity in clinical trials is persistent and is a threat to inclusivity and generalizabilityNeil Wallace, Stacey O'Keeffe, Heidi Gardner, et al.
Journal of Clinical Epidemiology|February 9, 2025
Lack of data collection in clinical trials prevents us from evaluating inclusion of people with disabilitiesShauna Cunningham, Amy M Russell, Emma Lidington, et al.
The Journal of Family Planning and Reproductive Health Care|June 12, 2014
Sexually transmitted infection incidence among adolescents in IrelandMartin P Davoren, Kevin Hayes, Mary Horgan, et al.
Pageof 10