Sanford Population Level Estimation of Type 1 Diabetes Risk GEnes in Children

Status: Recruiting
Location: See all (4) locations...
Intervention Type: Diagnostic test
Study Type: Observational
SUMMARY

In partnership with Helmsley Charitable Trust, the Sanford PLEDGE Study is a large-scale, observational, feasibility study of general population screening for T1D and celiac autoantibodies. Screening is incorporated into routine health care visits within an integrated health system.

Eligibility
Participation Requirements
Sex: All
Maximum Age: 17
Healthy Volunteers: t
View:

• Newborn Entry: Viable, term infants, defined as 36 weeks gestation by either dates or ultrasound who are born to pregnant women, 18 years or older, who are willing and able to provide informed consent (IC) prior to the onset of active labor. Who are born at a Sanford Health Hospital and plan to have routine well-child care at a Sanford Clinic

• Pediatric Entry: Children less than 6 years of age who receive their routine care at a Sanford facility and whose parents are able to provide IC.

• Adolescent Entry: Children, ages 9-16 years old, who receive their routine care at a Sanford facility and whose parents are able to provide IC.

• Siblings of children known to have T1D-relevant antibodies; ages 6 to 17 years old who receive care at a Sanford clinic

• Have an active MyChart account (with proxy access).

Locations
United States
Minnesota
Sanford Bemidji Region Clinics
RECRUITING
Bemidji
North Dakota
Sanford Bismarck Region Clinics
RECRUITING
Bismarck
Sanford Fargo Region Clinics
RECRUITING
Fargo
South Dakota
Sanford Sioux Falls Region Clinics
RECRUITING
Sioux Falls
Contact Information
Primary
Ann Mays, RN, CPN
ann.mays@sanfordhealth.org
605-312-6052
Time Frame
Start Date: 2020-07-17
Estimated Completion Date: 2031-03
Participants
Target number of participants: 33000
Treatments
Study Group
Children receiving routine care at a Sanford facility
Sponsors
Leads: Sanford Health
Collaborators: The Leona M. and Harry B. Helmsley Charitable Trust, University of Exeter, Pacific Northwest Research Institute

This content was sourced from clinicaltrials.gov