1.Evaluating informed consent during trial recruitment consultations: development and preliminary evaluation of a new method

作　　者：Julia Wade ;Daisy Townsend ;Daisy Gaunt 等

出　　处：Trials. 2015 ;16(2):1.doi:10.1186/1745-6215-16-S2-P118

出版社：BioMed Central

文章 ID：175814788

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2.Challenges of implementing multiple imputation to address missing data in economic evaluations

作　　者：Aida Moure Fernandez ;Kirsty Garfield ;Sian Noble 等

出　　处：Trials. 2015 ;16(2):1.doi:10.1186/1745-6215-16-S2-P26

出版社：BioMed Central

文章 ID：175815510

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3.Investigating the effectiveness and cost-effectiveness of FITNET-NHS (Fatigue In Teenagers on the interNET in the NHS) compared to activity management to treat paediatric chronic fatigue syndrome (CFS)/myalgic encephalomyelitis (ME): amendment to the published protocol

作　　者：Emma Anderson ;Daisy Gaunt ;Chris Metcalfe 等

出　　处：Trials. 2019 ;20(1):750-752.doi:10.1186/s13063-019-3895-1

出版社：BioMed Central

文章 ID：253248420

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4.Informed consent in randomised controlled trials: development and preliminary evaluation of a measure of Participatory and Informed Consent (PIC)

作　　者：Julia Wade ;Daisy Elliott ;Kerry N. L. Avery 等

出　　处：Trials. 2017 ;18(1):327.doi:10.1186/s13063-017-2048-7

出版社：BioMed Central

文章 ID：199309803

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5.Investigating the effectiveness and cost-effectiveness of FITNET-NHS (Fatigue In Teenagers on the interNET in the NHS) compared to Activity Management to treat paediatric chronic fatigue syndrome (CFS)/myalgic encephalomyelitis (ME): protocol for a randomised controlled trial

作　　者：Sarah Baos ;Amberly Brigden ;Emma Anderson 等

出　　处：Trials. 2018 ;19(1):136.doi:10.1186/s13063-018-2500-3

出版社：BioMed Central

文章 ID：213573435

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6.Defining the minimally clinically important difference of the SF-36 physical function subscale for paediatric CFS/ME: triangulation using three different methods

作　　者：Amberly Brigden ;Roxanne M Parslow ;Daisy Gaunt 等

出　　处：Health and Quality of Life Outcomes. 2018 ;16(1):202.doi:10.1186/s12955-018-1028-2

出版社：BioMed Central

文章 ID：219769978

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