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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04005560
Other study ID # RC19_0128
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 26, 2019
Est. completion date February 15, 2020

Study information

Verified date October 2020
Source Nantes University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to assess patient's quality of life 5 to 10 years after a severe bacterial infection with hospitalization in a intensive unit care. The population is derived from the DIABACT III study. The investigators will include every patient still alive. To evaluate our question, patients and their parents will answer quality of life questionnaires. The investigators will also have telephone interviews with the parents to know somatic and psychological effects on their child. The investigators will see if quality of life and sequelae differ depending on various studied factors.


Description:

The aim of this study is to assess patient's quality of life 5 to 10 years after hospitalization in intensive car unit for a severe bacterial infection. The population is derived from DIABACT III study, and includes all patients still alive. To evaluate their quality of life, patients and parents will answer specific questionnaries. The Pediatric Quality of Life inventory (PedSQL) has various versions for children depending on their age, adults and parents. The investigators will get physical, emotional, social and academic scores. To assess somatic and psychological effect after the severe bacterial infection, the investigators will have telephone interviews with the parents, with many questions about organs disorders, specialized medical follow-up, medication, need physical or material assistance, financial and psychological family impact… The investigators will examine data from DIABACT III study to assess determinants of the quality of life for these patients.


Recruitment information / eligibility

Status Completed
Enrollment 47
Est. completion date February 15, 2020
Est. primary completion date February 15, 2020
Accepts healthy volunteers No
Gender All
Age group 6 Years to 24 Years
Eligibility Inclusion Criteria: - Every patients from DIABACT III study still alive at the beginning of this study Exclusion Criteria: - Patients who did not respond to the questionnaire - Inability to contact the patient and family - No fixed postal address

Study Design


Related Conditions & MeSH terms


Intervention

Other:
no interventional study
no interventional study

Locations

Country Name City State
France CHU Nantes Nantes

Sponsors (1)

Lead Sponsor Collaborator
Nantes University Hospital

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary This quality of life will be evaluated by a questionnaire, the Pediatric Quality of Life inventory. The Pediatric Quality of Life inventory questionnaire has various versions depending on the patient age, from 5 years old to adult age. Patients will answers many questions in the academic, emotional, physical and social fields. It exists the same questionnaire adapted for parents. At the end, there is a score for each field and a total score. 6 months
Secondary Identify quality of life determinants. DIABACT III database has factors that could affect quality of life. 6 months
Secondary Assess long-term sequelae: evaluate somatic and psychological effects. We will have telephone interviews with the parents. During the telephone interview, we will ask many questions about organs disorders and psychological disorders (Strenghts and Difficulties Questionnaire), specialized medical follow-up, medication, need physical or material assistance, financial and psychological family impact 6 months
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