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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03954522
Other study ID # P/2018/354
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date June 1, 2019
Est. completion date February 1, 2021

Study information

Verified date May 2019
Source Centre Hospitalier Universitaire de Besancon
Contact Stéphanie NGUYEN
Phone 06.63.06.74.85
Email stephanielaurent@gmx.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

According to literature, it's difficult to evaluate the impact of the visit of the child in ICU. Currently, no recommendations are available regarding welcome and accompany children who visit their relative hospitalized in ICU. Collaboration between humanities and medical sciences brings to this question a complementary look. Majority of studies investigated the question of the impact of young child ICU visit in a unidirectional linear causality scheme visit = psychopathological impact. The visit of the child in ICU should not be considered as an isolated event whose objective characteristics would be alone vectors of trauma. Contrary, the child visit must be apprehended in relation to the quality of the supports on which the child can count. The investigators hypothesize that children can overcome the visit of a kin hospitalized in ICU if accompanying people can support the child and contain, before and after the visit, the emotions of the child.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 240
Est. completion date February 1, 2021
Est. primary completion date August 1, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 6 Years and older
Eligibility Inclusion Criteria:

- family groups in which at least one child aged 6 to 14 years having expressed the wish to visit his/her hospitalized relative

- family groups in which the non-hospitalized parent has expressed the wish to accompany his/her child during the visit

- parent hospitalized in ICU is at least 18 years old

- informed consent of children, non-hospitalized and/or hospitalized relatives

- informed consent of the accompanying caregiver

Exclusion Criteria:

- moribund patient

- child unaccompanied by his/her parent/relative during the visit

- non-hospitalized non-French-speaking parent/relative (need to be able to answer the questionnaires)

- child benefiting from a psychological follow-up prior to the hospitalization of his/her parent

- non French-speaking child

- child under 6 years old or older than 14

- hospitalized relative who died before the proposed interview with the child (particular attention will be carry out to the interview conditions. The loss of the hospitalized parent will not allow for an interview on the experience of the visit).

Study Design


Intervention

Other:
interview
Child = A clinical interview (recorded, duration approximately 30 min) and a scale of acute stress (IES child) will be performed at 2 times (during the 7 days following the first visit of hospitalized kin and 1 month after the kin was discharged from ICU) Accompanying parent/kin = Semi-directive interviews (recorded - duration approximately 30 min) will be performed at the same time as those of the child and will be recorded. The parent/kin will also complete a socio-demographic questionnaire of the family group and a depression anxiety scale (HADS) Nursing staff = A semi-directive interview (recorded - duration approximately 30 min) will be performed only once (during the 7 days following the first visit to the hospitalized kin). The caregiver will also complete a socio-demographic questionnaire and a Moral Distress Scale (MDS-R) Hospitalized parent = One month after ICU discharge, a depression anxiety scale (HADS) and an acute stress scale (IES) will be performed

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Besancon

Outcome

Type Measure Description Time frame Safety issue
Primary Acute psychotraumatic impact of the visit on the child Scale of stress (Child IES-R : Impact of Event Scale- Revised) : score calculated on 40 points.
A score of 17 or greater is considered as clinically relevant
7 days
Primary Chronic psychotraumatic impact of the visit on the child Scale of stress (Child IES-R : Impact of Event Scale- Revised) : score calculated on 40 points.
A score of 17 or greater is considered as clinically relevant
1 month
Primary Psychological experience of the visit for the child semi directive interview 7 days
Primary Parental, family and caregiver support provided to the child during and following the visit semi directive interviews of caregiver/family 1 month
Primary Psychological experience of the visit according the child age semi directive interview analysed in subgroup: comparison between child aged from 6 to 10 years old versus 11 to 14 years old 1 month
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