- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04370210
Sleep Quality During COVID-19 Containment in Children Whether or Not Usually Followed in Child Psychiatry (CONFIDODO)
Sleep Quality During COVID-19 Containment in Children 7 to 12 Years Old, Whether or Not Usually Followed in Child Psychiatry
Study Overview
Detailed Description
The coronavirus epidemic reached France in January 2020 and the WHO declared the COVID-19 outbreak was a pandemic on 11 March 2020. In response to this pandemic the French government announced national containment starting on 17 March 2020. Some recent studies suggest that a containment duration of more than 10 days and an extension beyond the originally announced duration would increase the psychological impact of it.
Sleep is a vital function that contributes to the proper neurophysiological and psychological development of human beings especially children. Sleep disorders can have a major impact on a child's behavior, mood, cognitive performance and metabolism. Sleep disorders are often associated with depression, anxiety and cognitive changes. Chronic sleep disorders are also risk factors for mental illness To our knowledge, no study targeting the quality of sleep in children who usually receive psychiatric care is underway or has been published. It is essential to ask what the quality of sleep in children with a psychiatric diagnosis who suddenly lose their bearings and their usual daily routine (school, therapeutic groups, day hospitals, etc.) after several weeks of containment.
This study is designed to assess different parameters in the 2 groups of children (healthy volunteers and Child with follow-up in child psychiatry) :
- the sleep quality,
- the depression level,
- the anxiety level,
- if socio-demographic factors have an influence on sleep disorders,
- if there is a correlation between children's sleep quality, and anxiety level / sleep quality in their parents.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Pontoise, France, 95300
- Centre Hospitalier René Dubos
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Child aged 7 to 11 years and 11 months included on the first day of containment in France on 17 March 2020
- Child receiving care at the CMP of Cergy-le-Haut (medico-psychological center) on the 2020 active patient population (at least one appointment with a child psychiatrist, a psychologist, a psychomotor therapist or a speech therapist or in a therapeutic group between January and March 2020)
OR
- Child not receiving any psychiatric care and having no siblings (half-brother, half-sister) followed in child psychiatry
- No parental opposition
Exclusion Criteria:
- Poor French reading comprehension by parents
- Objection of the child
- Child under guardianship, curatorship or foster care
- Child not on containment : child cared for outside his home everyday (in school and hospital daycare for example).
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Child without follow-up in child psychiatry
Child enrolled, and their parents, must complete online questionnaires
|
Child of both groups enrolled, and their parents, must complete online questionnaires
|
|
Child with follow-up in child psychiatry
Child enrolled, and their parents, must complete online questionnaires
|
Child of both groups enrolled, and their parents, must complete online questionnaires
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Comparison of sleep quality during COVID-19 containment between children usually followed in child psychiatry and children without follow-up
Time Frame: An average of 1 day
|
Sleep quality is assessed in both groups with the Sleep Disturbance Scale for Children (SDSC scale).
A score ≥ 45/125 is considered as pathological.
|
An average of 1 day
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Assessment of child depression in both groups
Time Frame: An average of 1 day
|
Child depression is measured using Child Depression Inventory Scale (CDI scale).
For each item the score is graded by severity from 0 (normal behavior) to 2 (severe).
|
An average of 1 day
|
|
Assessment of child anxiety in both groups
Time Frame: An average of 1 day
|
Child anxiety is measured using Revised Children's Manifest Anxiety Scale (RCMAS).
For each item, child answer by Yes or No.
The total score is interpreted using the correspondence tables in function of sex and age
|
An average of 1 day
|
|
Assessment of the influence of socio-demographic factors on sleep in both groups
Time Frame: An average of 1 day
|
Sleep quality is assessed with the Sleep Disturbance Scale for Children (SDSC scale).
The score obtained is interpreted in function of socio-demographic factors (age, sex, lifestyle, couple status, profession and socio-professional category, education)
|
An average of 1 day
|
|
Measure of the correlation between child sleep quality and parents sleep quality (anxiety level) in both groups
Time Frame: An average of 1 day
|
Sleep quality is assessed with the Sleep Disturbance Scale for Children (SDSC scale).
For their parents, sleep quality and anxiety level are measured with a numerical scale between 0 and 10.
For sleep quality, 0 correspond to a very poor quality and 10 to a very good quality.
For anxiety level, 0 correspond to no anxiety and 10 to a severe anxiety.
The score obtained for child is interpreted in function of their parents score.
|
An average of 1 day
|
|
Assessment of sleep disturbance based on psychiatry diagnoses in the group of children usually followed in child psychiatry
Time Frame: An average of 1 day
|
Sleep quality is assessed with the Sleep Disturbance Scale for Children (SDSC scale).
The score obtained is interpreted in function of child psychiatry diagnoses coded with Diagnostic and Statistical Manual of Mental Disorders (DSM-5)
|
An average of 1 day
|
|
Assessment of child anxiety based on psychiatry diagnoses in the group of children usually followed in child psychiatry
Time Frame: An average of 1 day
|
Child anxiety is measured using Revised Children's Manifest Anxiety Scale (RCMAS). For each item, child answer by Yes or No. The score obtained is interpreted in function of child psychiatry diagnoses coded with Diagnostic and Statistical Manual of Mental Disorders (DSM-5) |
An average of 1 day
|
|
Assessment of child depression based on psychiatry diagnoses in the group of children usually followed in child psychiatry
Time Frame: An average of 1 day
|
Child depression is measured using Child Depression Inventory Scale (CDI scale). For each item the score is graded by severity from 0 (normal behavior) to 2 (severe). The score obtained is interpreted in function of child psychiatry diagnoses coded with Diagnostic and Statistical Manual of Mental Disorders (DSM-5) |
An average of 1 day
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Erwan VION, Centre Hospitalier René Dubos
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
Keywords
Additional Relevant MeSH Terms
- Mental Disorders
- Nervous System Diseases
- Coronavirus Infections
- Coronaviridae Infections
- Nidovirales Infections
- RNA Virus Infections
- Virus Diseases
- Infections
- Respiratory Tract Infections
- Respiratory Tract Diseases
- Sleep Wake Disorders
- Pneumonia, Viral
- Pneumonia
- Lung Diseases
- COVID-19
- Dyssomnias
- Parasomnias
Other Study ID Numbers
- CHRD 0520
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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