The Experience of the Child With Cancer When Port à Cath Needle : Child's Speech

Pediatric Oncology Clinical Trial

— ELEAPort  

Official title:

The Experience of the Child With Cancer When Port à Cath Needle : Child's Speech

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05691816
• Other study ID #: 2022 USCLADE
• Status: Completed
• Start date: January 1, 2022
• Est. completion date: March 23, 2022

Study information

• Verified date: January 2023
• Source: University Hospital, Clermont-Ferrand
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

This qualitative research refers to the descriptive phenomenological method of Hurssel which allows an analysis of the experience and an understanding of the phenomenon. Semi-structured interviews are carried out with 10 children followed for cancer in 3 pediatric hemato-oncology departments. The children interviewed are aged 6 to 12 and can be with their parents. A thematic analysis approach is used to analyze the data of this research.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 10
• Est. completion date: March 23, 2022
• Est. primary completion date: March 23, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 6 Years to 12 Years

Eligibility

Inclusion Criteria:

• Child followed in pediatric oncology for cancer or hematological disease
• Child wearing a Port-a-cath needle placement and minimum use once a week

Exclusion Criteria:

• Child no speaking the French language

Related Conditions & MeSH terms

• Neoplasms
• Pediatric Oncology

Locations

Country	Name	City	State
France	CHU clermont-ferrand	Clermont-Ferrand

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Clermont-Ferrand

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Experience of self management of port-a-cath needle placement	Evaluation from the patients' point of view on how they self-manage a port a cath needle placement, semi-structured qualitative interviews with patients.	60 minutes