Neurocognitive Impact of Hypoglycemia in Type 1 Diabetes (HYPO)
|ClinicalTrials.gov Identifier: NCT00916838|
Recruitment Status : Active, not recruiting
First Posted : June 10, 2009
Last Update Posted : May 10, 2017
125 children with Type 1 Diabetes mellitis (T1DM) between 4 and 16 were recruited and 62 healthy siblings also enrolled in the study.
Children with T1DM and sibling controls ages 4 to 16 were assessed on memory and executive control skills at entry to the study (Test 1) and after two years of close monitoring for blood sugar events (Test 2). Diabetic children have their blood sugar tested directly before and after cognitive testing to ensure their blood sugar is within range during the testing. The 2-year follow-up period involves parents/child reporting any severe diabetic episode and periodically providing the results of the diabetic child's usual blood tests from their glucose monitoring device.
Children 7 and older also underwent high resolution MRI scans.
|Condition or disease|
|Type 1 Diabetes Mellitis|
|Study Type :||Observational|
|Actual Enrollment :||187 participants|
|Official Title:||Neurocognitive Impact of Hypoglycemia in Type 1 Diabetes|
|Study Start Date :||January 2003|
|Primary Completion Date :||March 2006|
|Estimated Study Completion Date :||December 2017|
Type 1 Diabetes Mellitis
Children with Type 1 Diabetes Mellitis (T1DM) between 4 and 16 were recruited.
Non diabetic Control
62 healthy siblings also enrolled in the study between the ages of 4 and 17.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00916838
|Principal Investigator:||Tamara G Hershey, PhD.||Washington Univeristy School of Medicine|