Decision Making and Future Planning for Children With Complex Illness

NCT ID: NCT02579577

Last Updated: 2017-05-03

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 32 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2015-10-31
• Study Completion Date: 2017-01-31

Brief 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. Outpatient 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.

Conditions

Long-Term Care; Palliative Care

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

Decision making cohort

Any people identified as being important within the network of care for children with life-limiting illnesses.

Observation

Intervention Type: OTHER

Observation of clinic appointments and ward rounds if the child is admitted to hospital during the study period.

Interviews

Intervention Type: OTHER

Semi-structured interviews will be conducted approximately 3 times during the study period with each participant.

Medical notes review

Intervention Type: OTHER

The child's electronic medical record will be accessed periodically to identify any planned appointments or periods of hospitalisation and their medical notes will also be reviewed at the end of the study.

Interventions

Observation

Observation of clinic appointments and ward rounds if the child is admitted to hospital during the study period.

Intervention Type: OTHER

Interviews

Semi-structured interviews will be conducted approximately 3 times during the study period with each participant.

Intervention Type: OTHER

Medical notes review

The child's electronic medical record will be accessed periodically to identify any planned appointments or periods of hospitalisation and their medical notes will also be reviewed at the end of the study.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Their child must be between 28 days and 18 years old
• Their child must have a LLI within categories 2-4 (Association for Children with Life-threatening and Terminal Conditions and their Families, 2004) (see page 8)
• Child must be under the care of a consultant at either of the two NHS Trusts included in the study
• The parent must be aware of the child's LLI diagnosis
• Participants must speak English. This is both due to resource constraints and due to the sensitive topic such that difficulties in translating questions sensitively may cause greater distress to participants.

• Children will be classed as participants if their parent is a participant and consents to their child's medical notes being accessed.
• For children to participate in the interview component of the study, they must be over the age of 7 years and cognitively able to provide their own assent (or consent, if over 16 years old)
• Parents must have agreed to the child's participation if they are under 16 years old
• Participants must speak English or be able to communicate in some way using alternative or augmentative communication.

• Significant others must have been identified by the eligible child and/or parents as being important in their decision making and future planning
• Participants must speak English
• Participants must be over the age of 7 years and provide their own assent alongside parental consent (if under 16 years old) or provide consent if they are over the age of 16 years (in the case of a friend or sibling being nominated as a 'significant other').

Exclusion Criteria

• Families and significant others of children with ACT Category 1 life-threatening illnesses (Conditions for which curative treatment may be feasible but can fail)

• Minimum Eligible Age: 28 Days
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

University of Nottingham

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Bridget Johnston, Professor

Role: PRINCIPAL_INVESTIGATOR

University of Nottingham

Locations

Sherwood Forest Hospitals NHS Trust

Mansfield, , United Kingdom

Nottingham University Hospitals NHS Trust

Nottingham, , United Kingdom

Sheffield Children's Hospital

Sheffield, , United Kingdom

Countries

United Kingdom

Other Identifiers

15068

Identifier Type: -

Identifier Source: org_study_id