We hypothesize that the use of comfort talk-techniques during venipuncture results in lower pain scores and less anxiety in children. The patient , parent and doctors' assistant will be more satisfied about the venipuncture in general.
ID
Bron
Verkorte titel
Aandoening
not applicable
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
To investigate if the use of comfort talk-techniques results in less pain during venipuncture in children
Achtergrond van het onderzoek
A venipuncture is for a lot of children a painful and stressfull procedure. Anxiety can induce the pain during the venipuncture and enlarge the stress and pain in a following blood withdrawal and even led to posttraumatic stress syndrome in children. Comfort talk-techniques are relaxation techniques, in which matching is used and negative suggestions are avoided. These comfort-talk techniques have been extensively evaluated in adults and give less pain, anxiety, medication use and complications. In children, it has not been properly investigated whether the use of comfort-talk techniques during painful procedures also causes less pain and anxiety.
Doel van het onderzoek
We hypothesize that the use of comfort talk-techniques during venipuncture results in lower pain scores and less anxiety in children. The patient , parent and doctors' assistant will be more satisfied about the venipuncture in general.
Onderzoeksopzet
5 months
Publiek
Wetenschappelijk
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
Use of lidocaïne/prilocaïne for local anesthesia, age 5 -18 (including 18) and sufficient understanding of the Dutch language.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
No use of lidocaïne/prilocaïne creme (EMLA) for local anesthesia, age <5 or > 18 years and insufficient understanding of the Dutch language
Opzet
Deelname
Voornemen beschikbaar stellen Individuele Patiënten Data (IPD)
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In overige registers
| Register | ID |
|---|---|
| NTR-new | NL8221 |
| Ander register | CMO Arnhem-Nijmegen approved the study as CMO light : 2019-5488 |