4PICU: Psycho-educational Tool to Prevent Psychological Sequelae Following Paediatric Intensive Care Unit Admission

Sponsor
Imperial College Healthcare NHS Trust (Other)
Overall Status
Recruiting
CT.gov ID
NCT04635449
Collaborator
Imperial College London (Other)
288
1
2
23
12.5

Study Details

Study Description

Brief Summary

  • 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.

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Age-specific information booklet and targeted telephone call
Phase 2/Phase 3

Detailed Description

STUDY OBJECTIVES AND PURPOSE

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
288 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Two-arm, parallel-group, single centre, randomised controlled trialTwo-arm, parallel-group, single centre, randomised controlled trial
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
A Prospective Randomised Controlled Study of a Directed Psycho-educational Tool to Prevent Psychological Sequelae Following Paediatric Intensive Care Admission.
Actual Study Start Date :
Jul 1, 2021
Anticipated Primary Completion Date :
Jun 1, 2023
Anticipated Study Completion Date :
Jun 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Intervention

age-specific information, complemented by a follow-up targeted telephone call

Other: 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.

No Intervention: Treatment as usual

usual information given at PICU discharge

Outcome Measures

Primary Outcome Measures

  1. post-traumatic stress symptoms in the parents/guardians [6 months post PICU discharge]

    measured using the Impact of Events Scale, a self-report questionnaire

Secondary Outcome Measures

  1. Parent/guardian general emotional state [6 months post PICU discharge]

    Hospital Anxiety and Depression Questionnaire

  2. Child post-traumatic stress and other emotional and behavioural problems [6 months post PICU discharge]

    Questionnaire

Eligibility Criteria

Criteria

Ages Eligible for Study:
0 Years to 16 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • All children and young people age 0-16 years

  • 36 weeks corrected gestational age

  • Admitted to PICU >24 hours Parent(s)/guardian aged >18 years

Exclusion Criteria:
  • • Children where treatment withdrawal is being considered

  • 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Imperial College Healthcare NHS Trust London United Kingdom

Sponsors and Collaborators

  • Imperial College Healthcare NHS Trust
  • Imperial College London

Investigators

  • Principal Investigator: Simon Nadel, MBBS, Imperial College Healthcare NHS Trust

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Imperial College Healthcare NHS Trust
ClinicalTrials.gov Identifier:
NCT04635449
Other Study ID Numbers:
  • 20SM6281
First Posted:
Nov 19, 2020
Last Update Posted:
Mar 24, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Mar 24, 2022