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The study team will perform a randomised controlled trial of the intervention vs treatment as usual in children 0-16 years, stratified according to age (< 4 years and > 4 years).
It is estimated that 288 children will be required to show a difference in outcome which is PTSD in parents and children.
Full description
STUDY OBJECTIVES AND PURPOSE
Aims
Primary Objective To determine if the psycho-educational intervention is superior to treatment as usual in reducing parental post-traumatic stress and other psychological symptoms measured at 6 months after PICU discharge.
Secondary Objectives
Delivery of the Psycho-educational Tool and Assessment of Parental/Guardian Stress on PICU Discharge
[Our aim in future, if the intervention is shown to be successful, is to translate the intervention tools into the most frequently encountered foreign languages.]
After obtaining informed consent prior to the child's discharge from PICU, a parental PICU stress screening questionnaire (18), will be given to all parents/guardians prior to discharge by the researcher or appropriately trained bedside PICU nurse.
Parents/guardians of all eligible children will be randomized using random allocation to receive either active intervention or treatment as usual (TAU).
Those randomised to the intervention group will be given the age-appropriate written psycho-educational tool prior to PICU discharge, by the researcher. The researcher will also explain the mechanism of the targeted telephone call to be delivered 4-6 weeks after PICU discharge.
• Telephone Call:
All parents/guardians randomised to the intervention group will be offered the directed targeted telephone call from the researcher at 4-6 weeks post hospital discharge.
The researcher will use a protocolised, scripted interview questionnaire to discuss the contents of the tool and any psychological problems arising post PICU discharge, as well as provide information to families of ways of managing these, including, when appropriate referral to GP and local mental health services.
The study team will record the key outcomes of the call to include:
Uptake rates and outcome; the number of families with impairing symptoms; and rates of referral to GPs and/or local mental health services.
Enrollment
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Inclusion criteria
Exclusion criteria
• Children where treatment withdrawal is being considered
Primary purpose
Allocation
Interventional model
Masking
288 participants in 2 patient groups
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Central trial contact
Becky Ward, BSc
Data sourced from clinicaltrials.gov
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