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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT04625842
Other study ID # 2020-087
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date September 1, 2020
Est. completion date December 1, 2021

Study information

Verified date May 2024
Source Universitair Ziekenhuis Brussel
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In order to improve quality of care at the department, the investigators will perform a focus group interview study with patients and family members. They will perform 6 (3 in the French, and 3 in the Dutch language) focus group interviews with patients and 6 (3 in the French, and 3 in the Dutch language) with family members.


Description:

In order to improve quality of care at the department, the investigators will perform a focus group interview study with patients and family members. They will perform 6 (3 in the French, and 3 in the Dutch language) focus group interviews with patients and 6 (3 in the French, and 3 in the Dutch language) with family members. Following research questions will be answered: - What elements of care (ie infrastructure, interpersonal contact, information, communication) are good to the opinion of patients and family members? - What elements of care can be improved? - What are priorities in improvement of the care for patients and families? - What actions could possibly be taken in order to improve the care for future patients? Because the radiotherapy ward exists of 3 clusters, one per type of treatment conducted, the investigators will perform 6 focus group interviews with patients (3 in the French, and 3 in the Dutch language) and 6 focus group interviews with family members (3 in the French, and 3 in the Dutch language). Investigators will collect sex, main diagnosis (of patients), age and nationality of all participants at the beginning of each focus group interview. They will transcribe all interviews verbatim and analyze them in Nvivo software as provided by the VUB. Participant characteristics will be analyzed by descriptive statistics.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 1, 2021
Est. primary completion date September 1, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion criteria for patients: - Patients (18+) who were treated for cancer, receiving radiotherapy, and followed thereafter in the UZ Brussel - Dutch and French speaking - Start date of treatment max 6 months before inclusion - Estimated sample size: 5-8 x 6 patients Inclusion criteria for family members: - All family members (+18) of patients who were treated for cancer, receiving radiotherapy, and followed thereafter in the UZ Brussel - Dutch and French speaking - Start date of treatment of patient max 6 months before inclusion - Estimated sample size: 5-8 x 6 family members

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Focus group interview
Group interview with patients who received radiation treatment

Locations

Country Name City State
Belgium UZ Brussel Brussel

Sponsors (1)

Lead Sponsor Collaborator
Universitair Ziekenhuis Brussel

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Quality of care To identify elements of care that need improvement by using open ended interview questions and interaction between different participants immediately after treatment
Primary Problem solving To identify solutions for problems in care by using open ended interview questions and interaction between different participants immediately after treatment
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