The objective of the study was to explore parental experiences of being offered participation in a previous neonatal research study involving venepuncture. The method employed was a questionnaire-based exploration of parents' attitudes in those approached to participate in a study of term and preterm immunization responses (Preterm Immunisation Study [PREMIS]). We explored experience of the initial approach, knowledge of study, venepuncture and views on research ‘in general’. In all, 59% of families responded. Highest response rates were for those participating in PREMIS (87% term/69% preterm) and lowest in decliners (34% and 35%). Responding parents participating in PREMIS were well informed, positive about research and did not find the v...
A paradigm shift from protecting children from possible research risks to ensuring they receive poss...
Background: Comparative effectiveness randomised controlled trials are powerful tools to resolve unc...
Background: When a child participates in a clinical trial, informed consent has to be given by the p...
Objective: To explore parents’ perceptions and experience of being approached for enrolment of their...
BACKGROUND: Interviews with neonatologists in a related study had revealed a degree of discomfort wi...
BACKGROUND: Neurodevelopment and growth are primary concerns when neonates are born extremely premat...
Aim: The aim of this study was to evaluate parents' perceptions when they were asked to enrol their...
BACKGROUND: Patient and Public Involvement (PPI) is a rich and valuable part of the process of plann...
Studies exploring parents' trial experiences generally relate to their understanding of the consent ...
OBJECTIVE: To describe the attitudes of neonatologists to trial related perinatal postmortem examina...
BACKGROUND: There are limited data on parental perception of infant participation in minimal risk an...
OBJECTIVE To explore parents' perceptions of their infants' participation in randomized control t...
Aim The aim of this study was to evaluate parents' perceptions when they were asked to enrol their ...
Background Patient and Public Involvement (PPI) is a rich and valuable part of the process of planni...
Background Although recruiting newborns is ethically challenging, clinical trials remain essential t...
A paradigm shift from protecting children from possible research risks to ensuring they receive poss...
Background: Comparative effectiveness randomised controlled trials are powerful tools to resolve unc...
Background: When a child participates in a clinical trial, informed consent has to be given by the p...
Objective: To explore parents’ perceptions and experience of being approached for enrolment of their...
BACKGROUND: Interviews with neonatologists in a related study had revealed a degree of discomfort wi...
BACKGROUND: Neurodevelopment and growth are primary concerns when neonates are born extremely premat...
Aim: The aim of this study was to evaluate parents' perceptions when they were asked to enrol their...
BACKGROUND: Patient and Public Involvement (PPI) is a rich and valuable part of the process of plann...
Studies exploring parents' trial experiences generally relate to their understanding of the consent ...
OBJECTIVE: To describe the attitudes of neonatologists to trial related perinatal postmortem examina...
BACKGROUND: There are limited data on parental perception of infant participation in minimal risk an...
OBJECTIVE To explore parents' perceptions of their infants' participation in randomized control t...
Aim The aim of this study was to evaluate parents' perceptions when they were asked to enrol their ...
Background Patient and Public Involvement (PPI) is a rich and valuable part of the process of planni...
Background Although recruiting newborns is ethically challenging, clinical trials remain essential t...
A paradigm shift from protecting children from possible research risks to ensuring they receive poss...
Background: Comparative effectiveness randomised controlled trials are powerful tools to resolve unc...
Background: When a child participates in a clinical trial, informed consent has to be given by the p...