Neurocognition in Congenital Central Hypoventilation Syndrome (CCHS)

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age3-85
SponsorDebra Weese-Mayer

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 volunteers

Qualifiers

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

Design model

Case-only

Time perspective

Prospective

Treatments tested in this trial

  • NIH Toolbox Cognition Battery

    Other intervention

    An app-based cognitive assessment of executive function, attention, memory, and language that takes approximately 45 minutes to complete on an iPad

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Neurocognitive Outcomes

Longitudinal neurocognitive outcomes in CCHS patients

Time frame
January 2016 - December 2030

Secondary outcomes

1

Neourcognitive Outcomes

Longitudinal neurocognitive outcomes based on participant age, PHOX2B genotype, and history of respiratory intervention

Time frame
January 2016 - December 2030

Other outcomes

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