Sickle Cell Disease Clinical Trials

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Peripheral Arterial Tonometry and Neurocognition in Sickle Cell Disease

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

Objective: Evaluate the relationship between nocturnal oxyhemoglobin saturation (SpO2) and neurocognitive functioning (working memory and verbal comprehension) in individuals (ages 12-25) diagnosed with sickle cell disease controlling for age, genotype, and social vulnerability. Secondary Objective: Assess differences in white matter integrity, silent cerebral infarcts, neuroinflammation, and functional connectivity among individuals (ages 12-25) diagnosed with sickle cell disease with and without sleep disordered breathing after controlling for age. Assess differences in self- and caregiver-reported mood and pain severity among individuals (ages 12-25) diagnosed with sickle cell disease with and without sleep disordered breathing after controlling for age. Exploratory

Objectives: Explore the relationship between nocturnal oxyhemoglobin saturation (SpO2) and neurocognitive functioning (attention, processing speed, verbal memory, visual memory, motor dexterity) in individuals (ages 12-25) diagnosed with sickle cell disease controlling for age, genotype, and social vulnerability. Assess the feasibility of an optical imaging tool (Speckle Contrast Optical Spectroscopy - Open-Motion 3.0) to measure cerebral blood flow and blood volume in patients diagnosed with sickle cell disease (ages 12-25). Assess the concordance between measurement of cerebral blood flow and volume using speckle contrast optical spectroscopy and arterial spin labeling brain MRI.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 12
Maximum Age: 25
View:

• Diagnosed with sickle cell disease of any genotype

• Participant in the Sickle Cell Clinical Research and Intervention Program

• Between 12-25 years of age at the time of enrollment

• English is the primary language

• Access to an electronic device with WiFi

Locations
United States
Tennessee
St. Jude Children's Research Hospital
RECRUITING
Memphis
Contact Information
Primary
Andrew Heitzer, PhD
referralinfo@stjude.org
888-226-4343
Backup
Stephanie Guthrie, RN, BSN
referralinfo@stjude.org
888-226-4343
Time Frame
Start Date: 2024-09-16
Estimated Completion Date: 2028-06
Participants
Target number of participants: 65
Sponsors
Leads: St. Jude Children's Research Hospital

This content was sourced from clinicaltrials.gov