About this trial
Congenital central hypoventilation syndrome (CCHS) is a rare disorder of autonomic and respiratory regulation that frequently alters oxygen delivery to the brain. In CCHS, neurocognitive function has been of great concern because of the potential for repeated hypoxemia and hypercarbia in activities of daily living in addition to hypoventilation with related hypoxemia and hypercarbia during sleep. As the world's leading referral center for CCHS, the Center for Autonomic Medicine in Pediatrics (CAMP) is engaged in ongoing research to identify factors that impact neurocognitive performance in patients with CCHS in order to optimize clinical management and improve long term neurocognitive outcomes.
The purpose of this IRB-approved research study is to implement the NIH Toolbox as a standard measurement of cognitive health in patients with CCHS. Further, the study aims to determine how intrinsic and extrinsic disease factors such as age at diagnosis, PHOX2B mutation type and genotype, and nature of past and present artificial respiratory intervention affect the NIH Toolbox Cognitive scores of individuals with CCHS. Eligible participants will complete a 45-minute NIH Toolbox assessment and parents (or adult participants) will complete an associated, 15-minute Research Electronic Data Capture (REDCap) questionnaire.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
PHOX2B mutation-confirmed CCHS diagnosis
Speaks and reads English as a primary language
Disqualifiers
Unsuspected or unconfirmed CCHS
Does not speak or read English as a primary language
Trial population
PHOX2B mutation-confirmed CCHS patients between 3-85 years of age, who speak and read English as a primary language.
Trial design
Case-only
Prospective
Treatments tested in this trial
NIH Toolbox Cognition Battery
Other interventionAn app-based cognitive assessment of executive function, attention, memory, and language that takes approximately 45 minutes to complete on an iPad
Treatment groups
Trial outcomes
Primary outcomes
Neurocognitive Outcomes
Longitudinal neurocognitive outcomes in CCHS patients
Secondary outcomes
Neourcognitive Outcomes
Longitudinal neurocognitive outcomes based on participant age, PHOX2B genotype, and history of respiratory intervention
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Debra Weese-Mayer
Lead sponsor
Ann & Robert H Lurie Children's Hospital of Chicago
Sponsor institution
Ann & Robert H Lurie Children's Hospital of Chicago
Collaborator
Seattle Children's Hospital
Collaborator
Children's Hospital Los Angeles
Collaborator
Children's Hospital of Philadelphia
Collaborator