- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT04924023
The Effect of Using a Kaleidoscope During Central Venous Catheter Dressing Changes in Children With Cancer
The Effect of Using a Kaleidoscope During Central Venous Catheter Dressing Changes on Anxiety and Pain in Children With Cancer: A Randomised Controlled Study
Panoramica dello studio
Stato
Intervento / Trattamento
Descrizione dettagliata
This was a randomised controlled trial with 60 children aged 6-12 diagnosed with cancer who were placed either in a kaleidoscope group (n=30) or a control group (n=30). Each child's anxiety was evaluated by the child using the Child Fear Scale before, during and after a central venous catheter dressing procedure, and each child's pain during and after the procedure was evaluated by the child using the Wong-Baker Faces Pain Rating Scale (WB-FACES). Each child's heart rate and oxygen saturation were measured with a pulse oximeter device before, during and after central venous catheter dressing.
The children in kaleidoscope group looked into the kaleidoscope and slowly turned it. This distraction procedure began immediately before the central venous catheter dressing and continued until it was finished.
No intervention was performed to reduce pain and anxiety for children in the control group.
Parents accompanied their children during the procedure in both groups.
Tipo di studio
Iscrizione (Effettivo)
Fase
- Non applicabile
Contatti e Sedi
Luoghi di studio
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Burdur, Tacchino
- Pınar BEKAR
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
- a cancer diagnosis,
- having a central venous catheter,
- 6-12 years old,
- not having taken any analgesics in the 6 hours before the central venous catheter dressing, -being in a non-terminal phase of the disease,
- absence of neutropenia,
- volunteering to participate in the study,
- the absence of any health problems that prevent communication in the parent or the child.
Exclusion Criteria:
-the reporting of pain for another reason at the time of the central venous catheter dressing.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Terapia di supporto
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
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Sperimentale: Kaleidoscope Group
Children in this group were told what a kaleidoscope is and how to use it before their central venous catheter dressing.
The children were then asked if they would like to look into the kaleidoscope.
The children looked into the kaleidoscope and slowly turned it.
The researcher asked the children about the colours and shapes seen inside the kaleidoscope.
This distraction procedure began immediately before the central venous catheter dressing and continued until it was finished.
The kaleidoscope was disinfected before each use.
A kaleidoscope was provided for all children in this group by the same researcher.
Parents accompanied their children during the catheter dressing.
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The children looked into the kaleidoscope and slowly turned it.
The researcher asked the children about the colours and shapes seen inside the kaleidoscope.
This distraction procedure began immediately before the central venous catheter dressing and continued until it was finished.
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Nessun intervento: Control Group
No intervention was performed to reduce pain and anxiety for children in the control group.
Parents accompanied their children during the procedure.
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
---|---|---|
Wong-Baker FACES Pain Rating Scale (WB-FACES)
Lasso di tempo: 5 MONTHS
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The Wong-Baker Faces Pain Rating Scale (WB-FACES) is used to evaluate pain levels in children.
This numeric rating scale ranges from 0 to 10 and is represented by faces that display emotions ranging from smiling (0 = very happy or no pain) to crying (10 = the worst pain).
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5 MONTHS
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Children's Fear Scale (CFS)
Lasso di tempo: 5 MONTHS
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The Children's Fear Scale (CFS) is used to evaluate anxiety levels in children.
It consists of five facial expressions representing a range from no anxiety (0) to severe anxiety (4).
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5 MONTHS
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
---|---|---|
Heart Rate
Lasso di tempo: 5 MONTHS
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The heart rate and oxygen saturation values of the children in both groups were measured and recorded by the researcher 3 minutes before the procedure, during the procedure and 5 minutes after the procedure using a pulse oximeter device.
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5 MONTHS
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Oxygen Saturation
Lasso di tempo: 5 MONTHS
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The heart rate and oxygen saturation values of the children in both groups were measured and recorded by the researcher 3 minutes before the procedure, during the procedure and 5 minutes after the procedure using a pulse oximeter device.
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5 MONTHS
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Collaboratori e investigatori
Sponsor
Investigatori
- Direttore dello studio: Emine EFE, Prof.Dr., Akdeniz University, Department of Child Health and Disease Nursing
Pubblicazioni e link utili
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Inizio studio (Effettivo)
Completamento primario (Effettivo)
Completamento dello studio (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- KAEK-791
Piano per i dati dei singoli partecipanti (IPD)
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Informazioni su farmaci e dispositivi, documenti di studio
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Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
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