Developing and evaluating multimedia information resources to improve engagement of children, adolescents and their parents with trials

Conditions

Long-term health conditions Not Applicable

Annegret Dahlmann‐Noor, John A. Greenwood, Andrew Skilton, Daniel H. Baker, Mohamed Abbas et al. (12 authors)

BMJ Open2024-07-015 citations

10.1136/bmjopen-2023-082472

Does digital, multimedia information increase recruitment and retention in a children’s wrist fracture treatment trial, and what do people think of it? A randomised controlled Study Within A Trial (SWAT)

Thirimon Moe‐Byrne, Peter Knapp, Daniel C. Perry, Juul Achten, Louise Spoors et al. (10 authors)

BMJ Open2022-07-0117 citations

10.1136/bmjopen-2021-057508

Supporting children and young people when making decisions about joining clinical trials: qualitative study to inform multimedia website development

Jacqueline Martin‐Kerry, Peter Knapp, Karl Atkin, Peter Bower, Ian Watt et al. (12 authors)

BMJ Open2019-01-0133 citations

10.1136/bmjopen-2018-023984

Developing and evaluating multimedia information resources to improve engagement of children, adolescents, and their parents with trials (TRECA study): Study protocol for a series of linked randomised controlled trials.

Martin-Kerry J, Bower P, Young B, Graffy J, Sheridan R, Watt I, Baines P, Stones C, Preston J, Higgins S, Gamble C, Knapp P.

2017-06-0822 citations

10.1186/s13063-017-1962-z

Interventions

Current interventions as of 04/05/2017: 1. Intervention group 1 (receives information about the trial by MMI plus standard participant information sheet) 2. Intervention group 2 (receives information

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Paediatric patients who are aged between 6-17 years who have a long-term health condition and are eligible to be recruited into a host clinical trial 2. Both female and male

Exclusion criteria

Exclusion criteria: 1. Paediatric patients who cannot participate in informed consent due to being too young (less than 6 years) or due to intellectual disability 2. Paediatric patients or their parents who do not speak English

Design outcomes

Primary

Measure	Time frame
Trial recruitment rates: the proportion of patients who agree to participate in the host trial, from the total number of patients approached, for each arm of the embedded trial at baseline.	—

Secondary

Measure	Time frame
1. Rates of retention of children and adolescents in the six host trials, measured by obtaining data on the number and timing of drop outs from each host trial at end/completion date of each of the six trials. 2. Quality of decision-making by respondents. The quality of decision-making by participants is a subjective outcome measure and will be measured at baseline through the completion of a quality of decision-making scale by children, adolescents and parents (as relevant).	—

Measure

Time frame

1. Rates of retention of children and adolescents in the six host trials, measured by obtaining data on the number and timing of drop outs from each host trial at end/completion date of each of the six trials. 2. Quality of decision-making by respondents. The quality of decision-making by participants is a subjective outcome measure and will be measured at baseline through the completion of a quality of decision-making scale by children, adolescents and parents (as relevant).

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Countries

England, United Kingdom

Contacts

Public ContactPeter Knapp

peter.knapp@york.ac.uk+44 (0)1904 321675

Outcome results

None listed