Teamwork, Targets, Technology, and Tight Control in Newly Diagnosed Pediatric T1D - 4T Study

Sponsor
Stanford University (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT04336969
Collaborator
National Institutes of Health (NIH) (NIH), National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) (NIH)
500
1
1
58.4
8.6

Study Details

Study Description

Brief Summary

The 4Ts program encompasses: Teamwork, Targets, Technology, and Tight Control. These methods will help patients better manage their condition of Type 1 Diabetes with improved patient reported outcomes.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: 4T Education and Care
N/A

Detailed Description

The goal of the 4T study is to implement proven methods and emerging diabetes technology into investigator's clinical practice to sustain tight glucose control from the onset of type 1 diabetes (T1D) and optimize patient reported and psychosocial outcomes. The investigators will define a program (4T - Teamwork, Targets, Technology, and Tight Control) translatable to Pediatric Diabetes clinics in the United States that reduces HbA1c and T1D burden and improves patient well-being.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
500 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Teamwork, Targets, Technology, and Tight Control in Newly Diagnosed Pediatric T1D - 4T Study
Actual Study Start Date :
Jun 18, 2020
Anticipated Primary Completion Date :
Apr 30, 2022
Anticipated Study Completion Date :
Apr 30, 2025

Arms and Interventions

Arm Intervention/Treatment
Other: T1D Patients

Participants will wear a Continuous Glucose Monitor (CGM) with remote data monitoring

Behavioral: 4T Education and Care
CGM data will be used to create customized weekly feedback to the participant/family by secure MyChart message.

Outcome Measures

Primary Outcome Measures

  1. Change in rise of HbA1c [Baseline, 6 months and 12 months post-diagnosis]

    Rise in HbA1c (a measure of blood sugar levels over the previous 3 months) as a measurement of the effect of 4T education and care. Collected through a blood sample.

Secondary Outcome Measures

  1. Change in CGM Benefits and Burden Scale [Baseline, 3, 6, 9 and 12 months]

    This tool measures the benefits and burden of Continuous Glucose Monitor (CGM) device use, and is reported by participants. PERCEIVED BENEFITS OF CGM SCALE (BenCGM): Below is a list of things people might think are good about wearing a CGM. 5 - Strongly agree 4 -Agree 3 - Neutral 2 - Disagree 1 - Strongly disagree

  2. Change Diabetes Distress Scale [Baseline, 3, 6, 9 and 12 months]

    This measure is widely used to capture the psychological distress experienced in relation to diabetes, and is reported by participants. Score Range: 0-4 Interpretation: Higher scores indicates higher distress, a worse outcome Not a Problem A Slight Problem A Moderate Problem Somewhat Serious Problem A Serious Problem A Very Serious Problem

  3. Change in Diabetes Technology Attitude Scale [Baseline, 3, 6, 9 and 12 months]

    This measure has questions on attitudes and use of various general technologies (e.g., smartphone) and diabetes devices, and is reported by participants. Tool lists statement and participants reports how much they agree with the statement. 1 2 3 4 5 Strongly disagree Disagree Neutral Agree Strongly agree

  4. Change in Parental Diabetes Distress Scale [Baseline, 3, 6, 9 and 12 months]

    The Parental Diabetes Distress Scale (PARENT-DDS) measure is widely used to capture the psychological distress experienced by parents in relation to diabetes, and is reported by participants. Score Range: 0-4 Interpretation: Higher scores indicates higher distress, a worse outcome Not a Problem A Slight Problem A Moderate Problem Somewhat Serious Problem A Serious Problem A Very Serious Problem

  5. Change in Promise Global Health Scale [Baseline, 3, 6, 9 and 12 months]

    This measure is widely used to capture general and overall health, and is reported by participants. PROMISE GLOBAL HEALTH SCALES 5, Excellent | 4, Very Good | 3, Good | 2, Fair | 1, Poor

  6. Change in Physical Activity, Youth Physical Activity Questionnaire (Y-PAQ) [Baseline, 3, 6 and 9 months]

    Youth Physical Activity Questionnaire (Y-PAQ) is a measure used to determine overall physical activity in the last 7 days, and is reported by participants. Score Range: 1 to 3. Interpretation: Higher scores indicate higher levels of physical activity, a better outcome.

  7. Change in Physical Activity, International Physical Activity Questionnaire (IPAQ) [Baseline, 3, 6 and 9 months]

    International Physical Activity Questionnaire (IPAQ) asks about physical activity and sedentary behavior in the last 7 days, and is reported by participants. Score Range: 1 to 3. Interpretation: Higher scores indicate higher levels of physical activity, a better outcome.

  8. Change in participant Hypoglycemic Fear Scale [Baseline, 3, 6 and 9 months]

    People with diabetes worry about hypoglycemia. Hypoglycemic Fear Survey (HFS-II) measure captures those worries and is reported by participants. Score Range: 0-4 Interpretation: Higher scores indicates higher levels of stress, a worse outcome

  9. Change in parent Hypoglycemic Fear Scale [Baseline, 3, 6 and 9 months]

    Parents of children with diabetes worry about hypoglycemia. Hypoglycemic Fear Survey (HFS-P) measure captures those worries and is reported by parents of participants. Score Range: 0-4 Interpretation: Higher scores indicates higher levels of stress, a worse outcome

  10. Change in Self-Efficacy for Exercise Scale [Baseline, 3, 6, and 9 months]

    Self-Efficacy for Exercise (SEE) Scale measures how confident people are in their ability to overcome barriers to exercise. Total scale is calculated by summing the responses to each question. The scale has a range of total scores from 0-90. A higher score indicates higher self-efficacy for exercise.

  11. Change in education exposure to safe exercise strategies [Baseline, 3, 6, and 9 months]

    Percentage of participants attending at least one telehealth session and a measure of education exposure to safe exercise strategies

Eligibility Criteria

Criteria

Ages Eligible for Study:
1 Year to 20 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

(Inclusion criteria includes all youth with new onset T1D seen in the Stanford/Lucile Packard Children's Hospital ages 1-21 years of age.

(NOTE: Investigators will include children and families who speak all languages using the Stanford interpreter services so as to have the greatest generalizability of the research. Questionnaires will only be given to English and Spanish speakers.)

  • All individuals within one month of T1D diagnosis seen at the Stanford Children's Diabetes Clinic

  • Individuals who plan to receive follow up care at the Stanford Children's Diabetes Clinic

  • Individuals who agree to CGM data integration into the EMR for remote monitoring

  • Age: six months to < 21 years of age

  • Patient or guardian must own and operate an Apple compatible device (e.g. iPhone or iPod Touch) to allow for Dexcom app and Apple HealthKit integration and transmission of GluVue remote data monitoring [Dr Prahalad's LPCH Auxiliary Fund grant (in addition to the R18) has resources to support iPod Touch purchase for participants who do not have these.]

Exclusion Criteria:
  • Diabetes diagnosis other than T1D

  • Diagnosis of diabetes > one month prior to initial visit

  • Individuals with the intention of obtaining diabetes care at another clinic

  • Individuals who do not consent to CGM use, CGM data integration, remote monitoring

  • Individuals > 21 years of age

Contacts and Locations

Locations

Site City State Country Postal Code
1 Stanford University, School of Medicine Stanford California United States 94304

Sponsors and Collaborators

  • Stanford University
  • National Institutes of Health (NIH)
  • National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Investigators

  • Principal Investigator: David M Maahs, MD, PhD, Lucile Packard Children's Hospital; Stanford University, School of Medicine

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
David Maahs, Chief of Pediatric Endocrinology, Stanford University
ClinicalTrials.gov Identifier:
NCT04336969
Other Study ID Numbers:
  • 52812
  • 1R18DK122422-01A1
First Posted:
Apr 7, 2020
Last Update Posted:
Feb 28, 2022
Last Verified:
Feb 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 28, 2022