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Type 1 DiabetesR2D2NCT05268250

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

A study testing R2D2 mHealth intervention in people with Type 1 Diabetes, run by Nemours Children's Clinic at 2 sites in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial 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… Read more about this study

Who is it for?
Ages 8 to 65 years
Conditions the study is for
Type 1 Diabetes
What is being tested?
R2D2 mHealth intervention
Could I receive a placebo?
No, everyone receives an active treatment
How many people
180 participants
Where
2 sitesUnited States
Study dates
26 Feb 2024to 31 Aug 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 8 to 65 years
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Who may be able to join

  • 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).

Who cannot join

  • 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.

Trial locations and contacts

2 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Susana R Patton, PhD contact

9046972000

susana.patton@nemours.org

Nicole Morales contact

nicole.morales@nemours.org

United States2 sites, 2 recruiting
  • Nemours Children's Health

    Jacksonville, Florida, 32207

    Susana R Patton, PhD, 9136973595, sp0105@nemours.org

    Amy Milkes, amy.milkes@nemours.org

    Recruiting
  • Children's Mercy Kansas City

    Kansas City, Missouri, 64108

    Mark Clements, MD PHD, 8162343000, endoclinicaltrials@cmh.edu

    Recruiting

Other trials in United States

About this study

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.

Read the 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.

Conditions
Type 1 Diabetes
Being tested
R2D2 mHealth intervention
Medical subject headings
Diabetes Mellitus, Type 1

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • R2D2 mHealth interventionBehavioural

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

Study groups in NCT05268250
Study groupRoleWhat they receive
R2D2 mHealth treatment for diabetes distressExperimentalThis is a mHealth supported, cognitive behavioral treatment for parents and school-age children who were identified with clinically relevant levels of diabetes distress as part of a clinic screening program
Receives: Behavioral: R2D2 mHealth intervention
Standard Care ControlNo interventionParents and school-age children who were identified with clinically relevant levels of diabetes distress as part of a clinic screening program will receive local resources (print or electronic).

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. youth glycated hemoglobin (HbA1c)

    proxy measure of average glycemic levels over 10-12 weeks

    Measured: week 0, week 13

  2. youth time in range

    based on continuous glucose levels, the percentage of time spent between 70-180mg/dl

    Measured: week 0, week 13

Secondary outcomes (4)
  1. Problem Areas in Diabetes-Child (PAID-C)

    validated child report of diabetes distress; range: 11-66, higher scores reflect greater distress

    Measured: week 0, week 13

  2. Parent Problem Areas in Diabetes-Child (P-PAID-C)

    validated parent report of diabetes distress; range 16-96, higher scores reflect greater distress

    Measured: week 0, week 13

  3. Diabetes Strengths and Resilience

    validated child report of resilience; range: 12-60, higher scores reflect greater resilience

    Measured: week 0, week 13

  4. Brief Resilience Scale

    validated adult report of resilience; range 1-5, higher scores reflect greater resilience

    Measured: week 0, week 13

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted7 Mar 2022
  2. Study start26 Feb 2024
  3. Primary completion31 Aug 2027 (estimated)
  4. Study completion31 Aug 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
180 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05268250
Sponsor's protocol ID
1687888
Acronym
R2D2
Status last verified
Aug 2026
First submitted
16 Feb 2022
Last updated
1 Sep 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing R2D2 mHealth intervention in people with Type 1 Diabetes, run by Nemours Children's Clinic at 2 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 1 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Susana R Patton, PhD (9046972000, susana.patton@nemours.org), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

youth glycated hemoglobin (HbA1c) (time frame: week 0, week 13). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Sep 2026.

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