- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04812210
Quality of Life and Neurodevelopment Assessment of Children With Congenital Heart Disease Aged 2 to 4 Years (QoLCHD)
Quality of Life and Neurodevelopment Assessment of Children With Congenital Heart Disease Aged 2 to 4 Years : a Multicentre Controlled Cross-sectional Study
Study Overview
Status
Conditions
Detailed Description
248 patients will be enrolled in this study (124 children in each group).
Patients from group 1 will be included during their annual medical check-up. HRQoL questionnaire, neurodevelopmental status scale and clinical status will be assessed during this site visit. No supplementary visit, directly related to the research, will be necessary. Three sites will participate to the study, members of he French national network for complex congenital heart diseases (M3C) .
Participants (healthy children) from group 2 will be included from kindergartens and schools. The prior agreement of the Ministry of National Education will be obtained before any procedure related to this study.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Montpellier, France, 34295
- Uh Montpellier
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion criteria:
- Children aged 2 to 4 years old.
- Group 2 : Chldren with CHD (as defined in the ACC-CHD classification).
Exclusion criteria:
- Other comorbidity affecting quality of life (polymalformative syndrome, extracardiac organ failure, severe genetic disease).
- Surgical procedure during the last 6 months.
- Inability to understand the HRQoL questionnaire (parents) :non-french speaker, severe intellectual disability.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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case: children with congenital heart disease aged 2 to 4 years.
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control children recruited in kindergartens and schools aged 2 to 4 years
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Comparison of the total score of the proxy HRQoL questionnaire
Time Frame: 1 day
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Comparison of the total score of the proxy HRQoL questionnaire (PedsQL 4.0 : Pediatric Quality of Life Inventory Version 4.0 Generic Core Scales) between patients with CHD and control children : The proxy HRQoL questionnaire PedsQL 4.0 is composed of 23 items comprising 4 demensions.
Items are reversed scored and linearly transformed to a 0-100 scale.
In order to get a total score we must sum all the items scores over the number of items answered on all the Scales.
If more than 50% of the items in the scale are missing, the scale scores should not be computed.
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1 day
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Comparison of score by dimensions of the proxy HRQoL questionnaire
Time Frame: 1 day
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Comparison of score by dimensions of the proxy HRQoL questionnaire (PedsQL 4.0 : Pediatric Quality of Life Inventory Version 4.0 Generic Core Scales) between patients with CHD and schoolchildren aged 2 to 4 years : The proxy HRQoL questionnaire PedsQL 4.0 is composed of 23 items comprising 4 demensions.
Items are reversed scored and linearly transformed to a 0-100 scale.
In order o get score by dimensions of scale we must sum the items scores over the number of items answered.
If more than 50% of the items in the scale are missing, the scale scores should not be computed.
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1 day
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Comparison of score of the roxy HRQoL questionnaire
Time Frame: 1 day
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Comparison of score of the roxy HRQoL questionnaire (PedsQL 4.0 : Pediatric Quality of Life Inventory Version 4.0 Generic Core Scales) to the type of the CHD unsing the ACC-CHD classification : The proxy HRQoL questionnaire PedsQL 4.0 is composed of 23 items comprising 4 dimensions.
Items are reversed scored and linearly transformed to a 0-100 scale.
In order to get a total score we must sum all the items scores over the number of items answered on all the Scales.
If more than 50% of the items in the scale are missing, the scale scores should not be computed.
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1 day
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Comparison of score of the proxy HRQoL questionnaire
Time Frame: 1 day
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Comparison of score of the proxy HRQoL questionnaire (PedsQL 4.0 : Pediatric Quality of Life Inventory Version 4.0 Generic Core Scales) to the severity of the CHD unsing the BETHESDA classification : The proxy HRQoL questionnaire PedsQL 4.0 is composed of 23 items comprising 4 demensions.
Items are reversed scored and linearly transformed to a 0-100 scale.
In order to get a total score we must sum all the items scores over the number of items answered on all the Scales.
If more than 50% of the items in the scale are missing, the scale scores should not be
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1 day
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Comparison of score of the HRQoL questionnaire
Time Frame: 1 day
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Comparison of score of the HRQoL questionnaire (PedsQL 4.0 : Pediatric Quality of Life Inventory Version 4.0 Generic Core Scales) to the patient functional status unsing the Ross classification : The proxy HRQoL questionnaire PedsQL 4.0 is composed of 23 items comprising 4 demensions.
Items are reversed scored and linearly transformed to a 0-100 scale.
In order to get a total score we must sum all the items scores over the number of items answered on all the Scales.
If more than 50% of the items in the scale are missing, the scale scores should not be
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1 day
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Comparison of score of the proxy HRQoL questionnaire
Time Frame: 1 day
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Comparison of score of the proxy HRQoL questionnaire (PedsQL 4.0 : Pediatric Quality of Life Inventory Version 4.0 Generic Core Scales) to the prognostic classification of the CHD unsing Davey B.T classification : The proxy HRQoL questionnaire PedsQL 4.0 is composed of 23 items comprising 4 demensions.
Items are reversed scored and linearly transformed to a 0-100 scale.
In order to get a total score we must sum all the items scores over the number of items answered on all the Scales.
If more than 50% of the items in the scale are missing, the scale scores should not be
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1 day
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Study of the association of the following variables related to the patient and to the CHD with the scores of the proxy HRQoL questionnaire
Time Frame: 1 day
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Study of the association of the following variables related to the patient and to the CHD with the scores of the proxy HRQoL questionnaire (PedsQL 4.0 : Pediatric Quality of Life Inventory Version 4.0 Generic Core Scales) . Univariate end multivariate analysis will be performed. The variables are:
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1 day
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Evaluation of the psychometric properties of the proxy HRQoL questionnaire
Time Frame: 1 day
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Evaluation of the psychometric properties of the proxy HRQoL questionnaire (PedsQL 4.0 : Pediatric Quality of Life Inventory Version 4.0 Generic Core Scales) .
for children aged 2 to 4 years old : The Pediatric Quality of Life Inventory Version 4.0 (PedsQLTM 4.0) is a questionnaire widely used in pediatric clinical trials.
This questionnaire was translated and linguistically validated in French, but no complete psychometric validation for French children aged 2 to 4 years has been performed yet.
Reliability and validity are considered the main measurement properties of such instruments
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1 day
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Chair: Johanna Calderon, PhyMeddExp
- Principal Investigator: Sophie Guillaumont, Saint Pierre Institute - Palavas les Flots
- Principal Investigator: Jean-Benoit Thmabo, Congenital Cardiology Department of university hospital of Bordeaux
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- RECHMPL21_0083
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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