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

NCT ID: NCT06960356

Last Updated: 2025-05-07

Study Results

Results pending

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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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

115 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-12-31

Study Completion Date

2025-12-31

Brief Summary

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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.

Detailed Description

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Conditions

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Stress Disorder, Post Traumatic

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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screening for post-resuscitation syndrome

Group Type EXPERIMENTAL

detect post-traumatic stress disorder

Intervention Type OTHER

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

Interventions

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detect post-traumatic stress disorder

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

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* 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

Exclusion Criteria

* 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
* Patient and/or parent refusal to participate
* No social security affiliation
* Patients / parents who do not speak French
Minimum Eligible Age

1 Year

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Grenoble

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Central Contacts

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Alice FUMAGALLI, PDE

Role: CONTACT

0676765503 ext. +33

Guillaume MORTAMET, PHD

Role: CONTACT

0476765503 ext. +33

Other Identifiers

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2024-A01670-47

Identifier Type: OTHER

Identifier Source: secondary_id

38RC24.0249

Identifier Type: -

Identifier Source: org_study_id

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