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Frances Shiely

Showing results (11-20 of 91) with videos related to

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Trials|December 4, 2023
How do trial teams plan for retention during the design stage of the trial? A scoping reviewEllen Murphy, Katie Gillies, Frances Shiely
Trials|November 18, 2022
How do trial teams plan for retention during the design stage of the trial? A scoping review protocolEllen Murphy, Katie Gillies, Frances Shiely
Plos One|August 12, 2025
Evaluating the use of SPIRIT on participant retention in randomised trials: Challenges in reporting and implications for practiceAmy O'Connor, Ellen Murphy, Frances Shiely
Trials|June 10, 2024
Retention strategies are routinely communicated to potential trial participants but often differ from what was planned in the trial protocol: an analysis of adult participant information leaflets and their corresponding protocolsEllen Murphy, Katie Gillies, Frances Shiely
European Journal of Public Health|September 22, 2009
Increased sexually transmitted infection incidence in a low risk population: identifying the risk factorsFrances Shiely, Mary Horgan, Kevin Hayes
International Journal of STD & AIDS|August 24, 2013
Comparison of risk factors for prevalent sexually transmitted infections based on attendees at two genitourinary medicine clinics in IrelandFrances Shiely, Kevin Hayes, Mary Horgan
Plos One|May 24, 2022
Information about dissemination of trial results in patient information leaflets for clinicals trials in the UK and Ireland: The what and the whenMatilda Bjorklund, Frances Shiely, Katie Gillies
Journal of Clinical Epidemiology|November 6, 2024
Use of participant data and biological samples is insufficiently described in participant information leafletsEmer R McGrath, Nigel Kirby, Frances Shiely
Plos One|January 22, 2024
How, and why, science and health researchers read scientific (IMRAD) papersFrances Shiely, Kerrie Gallagher, Seán R Millar
Trials|July 18, 2023
Clinical research nurse predictions of trial failure, recruitment and retention: a case for their early inclusion in trial designFrances Shiely, Danielle Murphy, Seán R Millar
Pageof 10

Showing results (11-20 of 91) with videos related to

Sort By:
Pageof 10
Trials|December 4, 2023
How do trial teams plan for retention during the design stage of the trial? A scoping reviewEllen Murphy, Katie Gillies, Frances Shiely
Trials|November 18, 2022
How do trial teams plan for retention during the design stage of the trial? A scoping review protocolEllen Murphy, Katie Gillies, Frances Shiely
Plos One|August 12, 2025
Evaluating the use of SPIRIT on participant retention in randomised trials: Challenges in reporting and implications for practiceAmy O'Connor, Ellen Murphy, Frances Shiely
Trials|June 10, 2024
Retention strategies are routinely communicated to potential trial participants but often differ from what was planned in the trial protocol: an analysis of adult participant information leaflets and their corresponding protocolsEllen Murphy, Katie Gillies, Frances Shiely
European Journal of Public Health|September 22, 2009
Increased sexually transmitted infection incidence in a low risk population: identifying the risk factorsFrances Shiely, Mary Horgan, Kevin Hayes
International Journal of STD & AIDS|August 24, 2013
Comparison of risk factors for prevalent sexually transmitted infections based on attendees at two genitourinary medicine clinics in IrelandFrances Shiely, Kevin Hayes, Mary Horgan
Plos One|May 24, 2022
Information about dissemination of trial results in patient information leaflets for clinicals trials in the UK and Ireland: The what and the whenMatilda Bjorklund, Frances Shiely, Katie Gillies
Journal of Clinical Epidemiology|November 6, 2024
Use of participant data and biological samples is insufficiently described in participant information leafletsEmer R McGrath, Nigel Kirby, Frances Shiely
Plos One|January 22, 2024
How, and why, science and health researchers read scientific (IMRAD) papersFrances Shiely, Kerrie Gallagher, Seán R Millar
Trials|July 18, 2023
Clinical research nurse predictions of trial failure, recruitment and retention: a case for their early inclusion in trial designFrances Shiely, Danielle Murphy, Seán R Millar
Pageof 10