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Remedy to Diabetes Distress (R2D2): A Scalable Screen to Treat Program for School-age Families

Remedy to Diabetes Distress (R2D2): A Scalable Screen to Treat Program for School-age Families

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05268250
Acronym
R2D2
Enrollment
180
Registered
2022-03-07
Start date
2024-02-26
Completion date
2027-08-31
Last updated
2026-09-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 1 Diabetes

Brief summary

This R01 is in response to RFA-DK-19-021, Treating Diabetes Distress to Improve Glycemic Outcomes in Type 1 Diabetes. The objective is to test the feasibility and acceptability of a novel, practical, and potentially scalable screen to treat program for diabetes distress in families of school-age children with T1D (called Remedy to Diabetes Distress \[R2D2\]) and to test the initial efficacy of R2D2 to reduce diabetes distress to improve children's glycemic control.

Detailed description

Only 22% of school-age children with type 1 diabetes (T1D) achieve an HbA1c of \<7.5% while the majority of school-age children who exceed this target are at higher risk for T1D-related complications. Achieving optimal T1D self-care is the only direct pathway to better HbA1c and even with the addition of modern therapeutic modalities (e.g., hybrid closed loop), it is a complex, time-consuming, and relentless task. School-age children cannot effectively manage T1D alone and require help from their parents to participate in daily T1D self-care. The research suggests that both parents and youth with T1D are vulnerable to Diabetes Distress (DD) and the American Diabetes Association (ADA) Standards of Care recommend ongoing assessment of DD in youth (starting at 7-8-years-old) and their caregiver during routine diabetes clinic visits. Unfortunately, while DD screening may be an ADA Care Standard, there are no practical treatment options for clinics to adopt to treat DD in school-age families in the case of positive screens. The researchers submit this new R01 in response to RFA-DK-19-021, Treating Diabetes Distress to Improve Glycemic Outcomes in Type 1 Diabetes. Our objective is to test the feasibility and acceptability of a novel, practical, and potentially scalable screen to treat program for DD in families of school-age children with T1D (called Remedy to Diabetes Distress \[R2D2\]) and to test the initial efficacy of R2D2 to reduce DD to improve children's glycemic control. To enhance scientific rigor, the researchers plan to use the ORBIT model for behavioral intervention development to guide the study design. The specific aims are: 1) Define feasibility and acceptability of our new screen to treat program (R2D2) for DD in school-age families, and 2) Establish initial efficacy of R2D2 to reduce parent and child DD to improve child glycemic control. The researchers propose to address these Aims through an iterative process and multiple projects to complete the necessary formative research to design, build, and prepare to implement R2D2. The researchers then propose to complete a Pilot randomized controlled trial of their R2D2 screen to treat program, testing for its initial efficacy based on child HbA1c and time in range (primary outcomes) and parent and child DD and resilience, and T1D self-care (secondary outcomes; Phase 2b: Pilot, n=180). The impact of the proposed R01 is high because it addresses a critical need for practical and evidence-based solutions for screening and treating DD in families of school-age children, heretofore an understudied patient subgroup. The researchers believe our study optimally responds to the FOA because the research team is multidisciplinary (anchored by a partnership between behavioral science and diabetology), and their R2D2 screen to treat program reflects a practical team approach that can realistically occur in clinic and scale to other centers.

Interventions

BEHAVIORALR2D2 mHealth intervention

R2D2 mHealth treatment will use cognitive behavioral therapy, mindfulness, and behavioral activation strategies

Sponsors

Nemours Children's Clinic
Lead SponsorOTHER
Children's Mercy Hospital Kansas City
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
8 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* child age between 8-12 years, physician confirmed T1D diagnosis, * either the child or the parent or both the child and parent report diabetes distress levels at or above clinical cut-points, * child is on an intensive insulin regimen (pump or MDI).

Exclusion criteria

* children on a conventional insulin regimen, children and/or parents who do not report diabetes distress levels at or above the clinical cut-points, * children who have an allergy or sensitivity to the adhesive and/or skin preparation used for CGM, children with a comorbid chronic condition (e.g., renal disease), * children and parents who do not speak English.

Design outcomes

Primary

MeasureTime frameDescription
youth glycated hemoglobin (HbA1c)week 0, week 13proxy measure of average glycemic levels over 10-12 weeks
youth time in rangeweek 0, week 13based on continuous glucose levels, the percentage of time spent between 70-180mg/dl

Secondary

MeasureTime frameDescription
Diabetes Strengths and Resilienceweek 0, week 13validated child report of resilience; range: 12-60, higher scores reflect greater resilience
Brief Resilience Scaleweek 0, week 13validated adult report of resilience; range 1-5, higher scores reflect greater resilience
Parent Problem Areas in Diabetes-Child (P-PAID-C)week 0, week 13validated parent report of diabetes distress; range 16-96, higher scores reflect greater distress
Problem Areas in Diabetes-Child (PAID-C)week 0, week 13validated child report of diabetes distress; range: 11-66, higher scores reflect greater distress

Countries

United States

Contacts

CONTACTSusana R Patton, PhD
susana.patton@nemours.org9046972000
CONTACTNicole Morales
nicole.morales@nemours.org
PRINCIPAL_INVESTIGATORSusana R Patton, PhD

Nemours Children's Health

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 2, 2026