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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02310724
Other study ID # DK61230-T2P2
Secondary ID U01DK061230
Status Completed
Phase
First received
Last updated
Start date March 1, 2014
Est. completion date January 17, 2020

Study information

Verified date July 2021
Source National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The primary objective of T2P2 is to track the progression of T2D and related comorbidities and complications in the TODAY cohort as they transition to young adulthood. We hypothesize that: - Youth-onset type 2 diabetes (T2D) will progress rapidly and result in high rates of diabetes-related medical complications and comorbidities. - The rapid rate of progression is related to increased insulin resistance characteristic of puberty, worse β-cell function, degree of glycemic control, control of non-glycemic factors, and obesity itself.


Recruitment information / eligibility

Status Completed
Enrollment 517
Est. completion date January 17, 2020
Est. primary completion date January 17, 2020
Accepts healthy volunteers No
Gender All
Age group 15 Years and older
Eligibility Inclusion Criteria: - Participated in TODAY clinical trial. Exclusion Criteria: -

Study Design


Related Conditions & MeSH terms


Intervention

Other:
TODAY cohort
This protocol is observation only and involves no intervention, care, treatment, or management.

Locations

Country Name City State
United States University of Colorado Denver Children's Hospital Aurora Colorado
United States Joslin Diabetes Center Boston Massachusetts
United States Massachusetts General Hospital Boston Massachusetts
United States Case Western Reserve University Rainbow Babies and Children's Hospital Cleveland Ohio
United States Baylor College of Medicine Houston Texas
United States Children's Hospital Los Angeles Los Angeles California
United States Yale University School of Medicine Department of Pediatrics New Haven Connecticut
United States Columbia University Naomi Berrie Diabetes Center New York New York
United States University of Oklahoma Health Science Center Oklahoma City Oklahoma
United States Children's Hospital of Philadelphia Philadelphia Pennsylvania
United States Children's Hospital of Pittsburgh Pittsburgh Pennsylvania
United States Saint Louis University Saint Louis Missouri
United States Washington University Saint Louis Missouri
United States University of Texas Health Sciences Center San Antonio Texas
United States SUNY Upstate New York University Syracuse New York

Sponsors (3)

Lead Sponsor Collaborator
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) National Eye Institute (NEI), National Heart, Lung, and Blood Institute (NHLBI)

Country where clinical trial is conducted

United States, 

References & Publications (2)

TODAY Study Group. Health Care Coverage and Glycemic Control in Young Adults With Youth-Onset Type 2 Diabetes: Results From the TODAY2 Study. Diabetes Care. 2020 Oct;43(10):2469-2477. doi: 10.2337/dc20-0760. Epub 2020 Aug 10. — View Citation

TODAY Study Group. Longitudinal Changes in Cardiac Structure and Function From Adolescence to Young Adulthood in Participants With Type 2 Diabetes Mellitus: The TODAY Follow-Up Study. Circ Heart Fail. 2020 Jun;13(6):e006685. doi: 10.1161/CIRCHEARTFAILURE. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary diabetic retinopathy a microvascular complication determined by fundus photography year 4
Primary microalbuminuria a microvascular complication determined by urine albumin excretion >= 30 mg/day every 12 months
Primary overt diabetic nephropathy a microvascular complication determined by glomerular filtration rate < 70 mL/min/1.73m2 every 12 months
Primary peripheral diabetic neuropathy a microvascular complication defined as the presence of Michigan Neuropathy Screening Instrument (MNSI) exam score >2 and <8 out of 10 appropriate responses to the Semmes-Weinstein monofilament (SW-MF) in either foot. every 12 months
Primary cardiac function a macrovascular (cardiovascular) risk indicator determined by echocardiogram year 2
Primary arterial stiffness a macrovascular (cardiovascular) risk indicator determined by pulse wave velocity year 5
Primary cardiovascular risk lipid values a macrovascular (cardiovascular) risk indicator determined by abnormal lipid value for LDL (>= 130 mg/dL) or triglycerides (>= 300 mg/dL) every 12 months
Secondary glycemic control determined by HbA1c (annual) every 12 months
Secondary psychological disorder determined by scores on the following participant self-report standard surveys: (a) the Beck Depression Inventory II (BDI-II), (b) the Patient Health Questionnaire (PHQ) scales for somatic symptoms, anxiety, and alcohol use; participants are also interviewed about emotional or mental health problems involving referral, treatment, or hospitalization, and psychiatric diagnoses made by a non-study source that can be confirmed according to standard study criteria from acquired medical records are also recorded every 12 months
Secondary body composition determined by body mass index (BMI) computed from physical measurements of height and weight every 12 months
Secondary insulin sensitivity and beta cell function determined by oral glucose tolerance test (at 6 and 9 years from randomization) to derive measures of insulin sensitivity (1/insulin0), insulin secretion (?C-peptide30-0/?glucose30-0, ?insulin30-0/?glucose30-0 if not on insulin), and the oral disposition index (oDI = insulin sensitivity x insulin secretion) participant years 6 and 9 from baseline
Secondary eating disorder determined by score on participant self report questionnaire Eating Disorder Diagnostic Scale (EDDS) every 12 months
Secondary health-related quality of life determined by score on the participant self report questionnaire Pediatric Quality of Life Inventory version 4.0 with age-specific versions for teen (13-18), young adult (19-25), and adult (=26) every 12 months
Secondary blood pressure determined by collection of blood pressure every 12 months
Secondary sleep function determined by scores on standard questionnaires and in-lab polysomnogram years 2-3
Secondary life stress determined by participant self report questionnaire based on the Yeaworth Adolescent Life Change Event Scale every 12 months
Secondary healthcare usage determined by participant self report about visits, referrals, treatments, tests, and procedures related to healthcare every 6 months
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