Digital, multimedia information resources (MMIs) containing text, video, animation and pictures are a promising alternative to written participant information materials designed to inform children, adolescents and parents about healthcare trials, but little research has tested whether they are fit for purpose. This study employed a consecutive groups design and user testing questionnaire to assess whether participants were able to find and understand key information in multimedia resources. Two rounds of testing were completed. In each round, seven children aged 7–11 tested the MMI with a parent; six adolescents aged 12–17 and seven parents tested the MMI independently. After round 1, the resources were revised based on participant scores, ...
Objectives To evaluate digital, multimedia information (MMI) for its effects on trial recruitment, r...
Background: Digital multimedia information (MMI) has potential for use in trial recruitment but ther...
BACKGROUND: Informed consent is a critical component of clinical research. Different methods of pres...
Digital, multimedia information resources (MMIs) containing text, video, animation and pictures are ...
Background: Randomised controlled trials are widely established as the best method for testing heal...
Background: Randomised controlled trials are widely established as the best method for testing healt...
Background Randomised controlled trials are widely established as the best method for testing health...
Objectives: To understand stakeholders’ views regarding the content and design of paediatric clinica...
© Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY. Published by BMJ. Objectives ...
Objectives: To understand stakeholders’ views regarding the content and design of paediatric clinica...
Objective: The study aim was to compare two methods of providing information about the BAMP (Bone An...
Objectives To understand stakeholders’ views regarding the content and design of paediatric clinical...
When planning paediatric trials, it is important to consider how best to communicate with children a...
ObjectivesTo evaluate digital, multimedia information (MMI) for its effects on trial recruitment, re...
OBJECTIVES: To evaluate digital, multimedia information (MMI) for its effects on trial recruitment, ...
Objectives To evaluate digital, multimedia information (MMI) for its effects on trial recruitment, r...
Background: Digital multimedia information (MMI) has potential for use in trial recruitment but ther...
BACKGROUND: Informed consent is a critical component of clinical research. Different methods of pres...
Digital, multimedia information resources (MMIs) containing text, video, animation and pictures are ...
Background: Randomised controlled trials are widely established as the best method for testing heal...
Background: Randomised controlled trials are widely established as the best method for testing healt...
Background Randomised controlled trials are widely established as the best method for testing health...
Objectives: To understand stakeholders’ views regarding the content and design of paediatric clinica...
© Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY. Published by BMJ. Objectives ...
Objectives: To understand stakeholders’ views regarding the content and design of paediatric clinica...
Objective: The study aim was to compare two methods of providing information about the BAMP (Bone An...
Objectives To understand stakeholders’ views regarding the content and design of paediatric clinical...
When planning paediatric trials, it is important to consider how best to communicate with children a...
ObjectivesTo evaluate digital, multimedia information (MMI) for its effects on trial recruitment, re...
OBJECTIVES: To evaluate digital, multimedia information (MMI) for its effects on trial recruitment, ...
Objectives To evaluate digital, multimedia information (MMI) for its effects on trial recruitment, r...
Background: Digital multimedia information (MMI) has potential for use in trial recruitment but ther...
BACKGROUND: Informed consent is a critical component of clinical research. Different methods of pres...