Psycho-educational Tool to Prevent Psychological Sequelae Following Paediatric Intensive Care Unit Admission
NCT ID: NCT04635449
Last Updated: 2022-03-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
PHASE2/PHASE3
288 participants
INTERVENTIONAL
2021-07-01
2023-06-30
Brief Summary
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* To confirm the effects of the psycho-educational tool on parent and child emotional adjustment 6 months after PICU discharge; and to explore whether these outcomes are associated with the child's age; with receipt of the targeted telephone call; and/or with parental levels of stress during the child's admission.
* To obtain detailed feedback from parents/guardians and children about the different aspects of the psycho-educational intervention (the written information and the targeted telephone call) and the utility of these two psycho-educational interventions.
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.
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Detailed Description
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Aims
* To systematically evaluate an innovative directed psycho-educational intervention consisting of written specific, age-appropriate information, complemented by a follow-up targeted telephone call in order to reduce psychological sequelae in the child and their parents/guardians after PICU discharge.
* To confirm the effects of the psycho-educational tool on parent and child emotional adjustment 6 months after PICU discharge; and to explore whether these outcomes are associated with the child's age; with receipt of the targeted telephone call; and/or with parental levels of stress during the child's admission.
* To obtain detailed feedback from parents/guardians and children about the different aspects of the psycho-educational intervention (the written information and the targeted telephone call) and the utility of these two psycho-educational interventions.
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
* To determine if the intervention is superior to treatment as usual in reducing child post-traumatic stress and other psychological symptoms measured at 6 months post PICU discharge.
* To determine whether the degree of parental stress during their child's PICU admission is particularly associated with the extent of psychological sequelae and whether the psycho-educational intervention is as less or more effective in the highly stressed families.
* To determine if adding this relatively simple, innovative and pragmatic intervention to treatment as usual will provide a cost-effective use of NHS resources
* To evaluate in detail child and parental acceptance of the intervention.
Delivery of the Psycho-educational Tool and Assessment of Parental/Guardian Stress on PICU Discharge
* Eligible families will include children 0-16 years admitted to PICU for \> 24 hours, surviving to be discharged.
* Parents who are deemed to lack adequate English Language to understand the written psycho-educational tool, telephone call and questionnaires will be excluded.
\[Our aim in future, if the intervention is shown to be successful, is to translate the intervention tools into the most frequently encountered foreign languages.\]
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.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
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Intervention
age-specific information, complemented by a follow-up targeted telephone call
Age-specific information booklet and targeted telephone call
age-specific information, complemented by a follow-up targeted telephone call to reduce psychological sequelae in the child and their parents after PICU discharge.
Treatment as usual
usual information given at PICU discharge
No interventions assigned to this group
Interventions
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Age-specific information booklet and targeted telephone call
age-specific information, complemented by a follow-up targeted telephone call to reduce psychological sequelae in the child and their parents after PICU discharge.
Eligibility Criteria
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Inclusion Criteria
* \> 36 weeks corrected gestational age
* Admitted to PICU \>24 hours Parent(s)/guardian aged \>18 years
Exclusion Criteria
* Life expectancy \<6 months
* Previous admission to Paediatric, or Neonatal Intensive Care for \> 24 hours, in the last 12months preceding the current PICU admission
* Parent(s)/ guardian to have insufficient English to complete questionnaires
* Overseas address
0 Years
16 Years
ALL
No
Sponsors
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Imperial College London
OTHER
Imperial College Healthcare NHS Trust
OTHER
Responsible Party
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Principal Investigators
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Simon Nadel, MBBS
Role: PRINCIPAL_INVESTIGATOR
Imperial College Healthcare NHS Trust
Locations
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Imperial College Healthcare NHS Trust
London, , United Kingdom
Countries
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Central Contacts
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Facility Contacts
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Simon Nadel
Role: primary
References
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Bridges K, Vickers B, Mitting RB, Cooper M, Garralda E, Nadel S. Directed psychoeducational tool to prevent psychological sequelae following paediatric intensive care admission: a prospective randomised controlled study (the 4PICU study). Arch Dis Child. 2025 Sep 27:archdischild-2025-328691. doi: 10.1136/archdischild-2025-328691. Online ahead of print.
Other Identifiers
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20SM6281
Identifier Type: -
Identifier Source: org_study_id
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