Development of Follow-up Nursing Consultations for Children at Risk of Post-resuscitation Syndrome

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age1-18
SponsorUniversity Hospital, Grenoble

About this trial

The investigator hypothesize that, during an IPDE consultation 3 months after discharge from critical care, the investigator will identify PTSD in approximately one-third of children, and show an association between this syndrome and quality of life in children admitted to pediatric intensive care.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients aged between 1 and 17.5 years at inclusion

Having stayed in a paediatric intensive care unit in one of the 2 participating centers: Lyon or Grenoble

Requiring mechanical ventilation (invasive or non-invasive) for more than 24 hours

Disqualifiers

Patients already under the care of a psychologist or psychiatrist

patients who died during their stay in intensive care

Patients who died between discharge and 3 months

Patients suspected of abuse

Trial design

Design model

Single group

Treatments tested in this trial

  • detect post-traumatic stress disorder

    Other intervention

    recommendation for follow-up by a professional specializing in child development and/or a complementary medical consultation

Treatment groups

115 Participants
are divided into 1 treatment group
Group A: screening for post-resuscitation syndromeExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

post-traumatic stress disorder

Prevalence of post-traumatic stress disorder (PTSD) as defined by a standardized assessment of PTSD using the Children's Revised Impact of Event Scale (CRIES-13) scale for children over 7 years of age. Range from 0 to 80. Higher scores indicate greater post-traumatic stress

Time frame
3 months

Secondary outcomes

1

Pediatric Quality of Life Inventory TM (PEDSQL scale)

assessing Pediatric Quality of Life Inventory TM (PESQL scale) at 3 months in patients admitted to pediatric critical care. Range from 0 to 230. Higher scores indicate better health related quality of life.

Time frame
3 months
2

correlation between the PTSD score and the child's quality of life

correlation between the post-traumatic stress disorder score (Using Children's Revised Impact of Event Scale - range from 0 to 65 - the higher the score, the greater the impact of the event on the child) and the child's quality of life ( Using Pediatric Quality of Life Inventory TM scale - range from 0 to 230 - higher scores indicate better health-related quality of life)

Time frame
3 months
3

Measurement of the association between the characteristics of children and their stay in critical care, and the presence of PTSD

Search for factors associated with the onset of PTSD. Measurement of the association between the characteristics of children and their stay in critical care, and the presence of PTSD (using the Children's Revised Impact of event Scale - Range from 0to 65 - the higher the score, the greater the impact of the event on the child)

Time frame
3 months
4

number of children with significant somatic symptoms

Estimate the proportion of children presenting significant and disabling somatic symptoms in their lives, requiring referral to the appropriate healthcare professionals.

Time frame
3 months

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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