Improvement of Anxiety Management During a Venous Puncture About Children With a Participatory Entertainment Method

  • STATUS
    Recruiting
  • End date
    Jun 30, 2022
  • participants needed
    136
  • sponsor
    University Hospital, Brest
Updated on 6 October 2021
anxiety

Summary

The purpose of this study is to demonstrate an anxiety decrease about children 3 to 6 years during a venous puncture with the "fabrique histoire".

Description

The purpose of this study is to demonstrate an anxiety decrease about children 3 to 6 years during a venous puncture with the "fabrique histoire".

the study will compare the "fabrique histoire"(Lunii(R)) with the usual care.

Details
Condition ANXIETY NEUROSIS, Anxiety Disorders (Pediatric), Generalized Anxiety Disorder (GAD), Generalized Anxiety Disorder (GAD - Pediatric), Anxiety Disorders, anxiety disorder
Treatment Usual Care, "fabrique à histoire"
Clinical Study IdentifierNCT04200196
SponsorUniversity Hospital, Brest
Last Modified on6 October 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Children 3 to 6 years in pediatric emergency needing to venous puncture
Oral consent by children
Informed and signed consent by tenured of parent authority
To have Anaesthetic patch 45 minutes or more before the venous puncture

Exclusion Criteria

To have Anaesthetic patch less than 45 minutes before the venous puncture because of necessity to blood test or an other emergency
Necessity to analgesic 3 emergency
Necessity to MEOPA
Minor parents
Assessment of anxiety is not possible because of comorbidity
Anterior participation to these study
Clear my responses

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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