Clinical trial
Overview: Use of Respiratory Support At Home in Children
Opening soon · Not applicable · 1 countries · Registry ID NCT06692660
Opening soonNot applicableObservational
What this study is about
the primary outcome is to describe the perceived success of the use of the respiratory support from the parent's point of view
A promising-looking record is not the same as confirmed eligibility. The study team must review the full criteria and current recruitment status.
Basic eligibility
Age0 Years to 17 Years
SexAll
Healthy volunteersNot accepted
ConditionSleep Apnea Syndromes in Children, Obesity in Children, Bronchopulmonary Dysplasia (BPD), Neuromuscular Disease, Storage Disease, Malformation, Alveolar Hypoventilation
Full registry criteria
Inclusion Criteria: * Children with respiratory support at home * Age 0 to 18 (not yet passed) years old Exclusion Criteria: * Palliative care * Invasive ventilation * High flow oxygen therapy
Treatments and study arms
The registry does not list a named intervention.
Primary outcomes
describe the perceived success of the use of the respiratory support from the parent's point of viewAssessment during the filling of the questionnaire at enrollment
The primary outcome measure is the median score and interquartile range, obtained from the answer modalities according to the Likert scale (scores ranging from 1 to 5), in response to the question from the parent interview guide, which states: "Do you consider that the ventilatory support proposed for your child is a success? Please circle the corresponding score."
Study locations
2 locations were listed when this page was built. The first 40 are shown.
Centre Hospitalier Universitaire Grenoble Alpes🇫🇷 Grenoble, Isère, France
Centre Hospitalier Grenoble Alpes🇫🇷 La Tronche, France
Eglantine HULLO, MDContact
Camille BERTIN, InternContact
Julie CASSIBBA, MDContact