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Active NON-SBIR/STTR RPGS NIH (US)

Pragmatic Clinic-Based Trial of a Mindfulness Based Intervention for Mood Concerns in Youth with Type 1 Diabetes

$7.53M USD

Funder NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES
Recipient Organization Children'S Research Institute
Country United States
Start Date Sep 05, 2024
End Date Jul 31, 2029
Duration 1,790 days
Number of Grantees 1
Roles Principal Investigator
Data Source NIH (US)
Grant ID 10981344
Grant Description

PROJECT SUMMARY / ABSTRACT Type 1 diabetes (T1D) is one of the most common chronic illnesses of childhood. The involved treatment regi- men, including daily insulin administration/pump management, frequent blood glucose checks, and careful tracking of food intake, places a high stress burden on patients. Adolescence is a risky time for T1D

management given a marked decline in treatment adherence. Over 80% of adolescents with T1D have glycemic control that does not reach target levels (A1c 7.0%), and one significant risk factor is the increase in negative affectivity, including depression and anxiety symptoms. Elevated depression and anxiety symptoms

affect 40% of teens with T1D. Our preliminary data support the notion that negative affectivity contributes to diminished treatment adherence and worsening of glycemia, partially through the effects of negative affectivity on stress-related behavior such as maladaptive eating behavior. The use of novel, targeted

interventions, tailored for the developmental needs of adolescents with T1D and the particular burdens of coping with their chronic illness, that are translatable and able to be disseminated into clinics are needed. Our pilot work adapted, with the collaboration of stakeholders, a 7-week, group mindfulness-based intervention

based on Learning to BREATHE, BREATHE-T1D, and a health education comparison condition, HealthEd- T1D, for adolescents with T1D. This pilot study demonstrated the feasibility and acceptability of participation in both groups with the ultimate goal of improving glycemic control via improvements to mood and therefore less

disordered eating, avoidant coping, less impulsivity, and better self-care. The primary goal of the current proposal is to conduct a full-scale efficacy trial of BREATHE-T1D as compared to HealthEd-T1D across two sites, Children’s National Hospital in Washington, DC and the University of Colorado in Denver. The study will

be a pragmatic clinical trial with another primary aim to conduct a pilot feasibility study of implementation of a group-based intervention for negative affect via an in-clinic screening and program referral process consistent with the Fit to Context Framework’s Design Phase. The feasibility and acceptability of the screening and

referral process will be assessed via documentation of screening rates as well as qualitative interviews and implementation survey measures with clinic staff and providers. This goal is to evaluate the screening and referral process into the program within the ultimate setting in which it will be delivered, if efficacious. The

result of the current study will be a feasible and acceptable clinic screening and referral process across multiple clinics and an efficacious group-based, virtual intervention tailored for adolescents with T1D designed for the settings in which it will ultimately be implemented. The multidisciplinary and multi-site study team

contributes complementary areas of expertise in adolescents with T1D, behavioral intervention development, negative affectivity and maladaptive eating behavior, adolescent mindfulness-based intervention, culturally- relevant care, qualitative data analysis, and dissemination and implementation.

All Grantees

Children'S Research Institute

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