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Insul-In This Together Program for Adolescents With Type 1 Diabetes and Their Parents (IITT)

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Stanford University

Status

Completed

Conditions

Type 1 Diabetes

Treatments

Behavioral: Insul-In This Together

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT04589689
1K23DK121771-01A1 (U.S. NIH Grant/Contract)
58372

Details and patient eligibility

About

The "Insul-In This Together" intervention is designed for teens with Type 1 Diabetes and their parents. This study seeks to evaluate an evidence-based family intervention for teens with type 1 diabetes and their parents to offset the psychosocial and diabetes self-management risks. This information will provide a more in-depth understanding of family-based program efficacy for teens with adolescents and provide more judicious and streamlined intervention options to be offered in diabetes clinics in the future.

Full description

This study will collect survey and biomedical data to assess this program in a randomized controlled trial with 165 families (including an adolescent and parent/caregiver) will be enrolled, complete surveys, provide biomedical data via continuous glucose monitors and receive a 6-week psychosocial intervention. The results of this study will inform future intervention redesign to provide more judicious interventions to be disseminated across diabetes care.This study will evaluate the relative efficacy of each of the individual intervention components and also identify the mechanisms of actions (mediators) that are most impacted by these types of interventions as well as most linked to long-term outcomes for adolescents.

Enrollment

366 patients

Sex

All

Ages

12+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Teen subject has a type 1 diabetes (T1D) diagnosis according to ADA criteria for at least 6 months
  2. Teen subject is age 12-19 years at time of screening (no age limit for parent participants)
  3. Participation of at least one cohabitating parent/caregiver.

Exclusion criteria

  1. Subject lacks access to a smartphone or Wi-Fi via computer
  2. Subject has restricted or no English proficiency
  3. Subject has a pervasive developmental, cognitive, or psychiatric limitations that compromise participation in study

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

366 participants in 2 patient groups

Intervention Group
Experimental group
Description:
The intervention group will participated in the The Insul-In This Together intervention, which consists of 6 weekly 30-minute online family sessions to discuss topics related to diabetes distress and parent-teen communication. Sessions include structured education, discussions, and skill-building activities related to parental involvement, parental monitoring, and parent-adolescent conflict. The intervention will be conducted by the PI or clinically trained research staff via Zoom. Online surveys, and glucose monitoring data will be captured at baseline and 3,6 and 12-month follow-ups. Brief surveys will also be conducted at 2-, 4-, and 6-week follow-ups (after every 2 sessions for the intervention group and later the control group). Participants will be asked to provide A1C test results that will be collected via chart review or from participants sharing their test results at baseline, 6-month, and 12-month follow-up.
Treatment:
Behavioral: Insul-In This Together
Waitlisted Control Group
Experimental group
Description:
The waitlisted control group will receive the same intervention as the intervention group, but at the 6-month follow-up mark. The intervention will be conducted by the PI or clinically trained research staff via Zoom. Online surveys, and glucose monitoring data will be captured at baseline and 3,6 and 12-month follow-ups. Brief surveys will also be conducted at 2-, 4-, and 6-week from baseline. Participants will be asked to provide A1C test results that will be collected via chart review or from participants sharing their test results at baseline, 6-month, and 12-month follow-up.
Treatment:
Behavioral: Insul-In This Together

Trial documents
2

Trial contacts and locations

1

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Central trial contact

Jessie J Wong, PhD; Haley Linzmeyer, MA

Data sourced from clinicaltrials.gov

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