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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03832790
Other study ID # 19-0186
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 4, 2019
Est. completion date June 30, 2023

Study information

Verified date September 2023
Source University of Colorado, Denver
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Despite advancements in care, most adolescents with T1D have higher BMI and significantly higher HbA1c than recommended and are markedly IR, placing them at increased risk for CVD1,2. Thus, alternative approaches to improve and maintain glycemic control, IR, and BMI for adolescents with T1D are urgently needed. This proposal moves beyond the current insulin and carbohydrate counting-focused lifestyle change paradigm to focus on sleep and circadian misalignment, which will allow for identification of new mechanisms that can be directly translated into future intervention and prevention trials. The goal of the current study is to utilize multiple objective measures of sleep duration, timing (actigraphy), and circadian rhythm (melatonin) in adolescents with type 1 diabetes (T1D; N = 40) and examine relationships with glycemic control, IR, vascular health, and BMI. Further, qualitative methodology will be used to identify barriers and facilitators to healthy sleep in adolescents with T1D.


Recruitment information / eligibility

Status Completed
Enrollment 23
Est. completion date June 30, 2023
Est. primary completion date May 31, 2023
Accepts healthy volunteers
Gender All
Age group 14 Years to 19 Years
Eligibility Inclusion Criteria: - attending high school - diagnosis of type 1 diabetes >1 year Exclusion Criteria: - current diagnosis of a sleep disorder (e.g., insomnia, OSA) or abnormal scores on sleep disorders screening measures - regular use of medications affecting sleep (e.g., stimulants, atypical antipsychotics, melatonin, other sleep aids) - HbA1c =11 or >14% for the previous 2+ measurements - IQ<70 or severe mental illness

Study Design


Intervention

Other:
observation
observation

Locations

Country Name City State
United States University of Colorado Anschutz Medical Campus/Children's Hospital Colorado Aurora Colorado

Sponsors (4)

Lead Sponsor Collaborator
University of Colorado, Denver Colorado Clinical & Translational Sciences Institute, Juvenile Diabetes Research Foundation, Ludeman Family Center for Women's Health Research

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary HbA1c HbA1c at 60 days
Primary glycemic variability CGM glucose SD at 2 weeks
Primary insulin sensitivity from hyperinsulinemic euglycemic clamp Si at study entry (baseline)
Primary BMI body mass index at study entry (baseline)
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