Decision making and future planning for children with complex illness
Research type
Research Study
Full title
Decision making and future planning for children with complex illnesses: a qualitative multi-stakeholder, longitudinal study
IRAS ID
165505
Contact name
Emma Popejoy
Contact email
Sponsor organisation
University of Nottingham
Clinicaltrials.gov Identifier
15CS028, Nottingham University Hospitals NHS Trust R&I
Duration of Study in the UK
1 years, 1 months, 28 days
Research summary
The population of children with life-limiting illnesses (LLI) in England is increasing and there is growing need to improve the quality of children’s palliative care. Families of children with LLI are confronted with many care decisions for their children, such as whether and when to commence artificial nutrition or ventilation. They may also have the opportunity to consider the care that may be appropriate for their child in the future. Despite the important decisions families and professionals are required to make, there is little empirical evidence regarding the process of decision making and future planning for this population. Few studies have investigated the perspectives of multiple stakeholders and none have addressed multiple perspectives longitudinally. Therefore the relational and contextual aspects of decision making and future planning for children with LLI have as yet not been identified.
A multiple-embedded case study utilising ethnographic methods (semi-structured interviews, observation and notes-review) is proposed to address this knowledge gap. Families of children with LLI cared for in either of two participating hospitals will be recruited and followed-up for up to 12 months. The family will be invited to nominate ‘significant others’ (e.g. relatives, friends, health care professionals) who assist them in decision making and future planning, to participate in the study. Out-patient clinic appointments or ward-rounds during periods of hospitalisation will be observed and semi-structured interviews will be conducted approximately three times with each participant. Medical notes will be reviewed at the end of the study.
This research will enable a better understanding of the experiences and preferences for engaging in decision making and future planning from the perspectives of all stakeholders. It will also provide an awareness of the communication practices involved in discussions and the networks of care surrounding children with LLI, including specific support needs in relation to their role.
REC name
East Midlands - Nottingham 1 Research Ethics Committee
REC reference
15/EM/0377
Date of REC Opinion
30 Sep 2015
REC opinion
Further Information Favourable Opinion