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Behavioral Economic Incentives to Improve Glycemic Control Among Adolescents and Young Adults

Behavioral Economic Incentives to Improve Glycemic Control Among Adolescents and Young Adults

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02568501
Enrollment
90
Registered
2015-10-06
Start date
2016-01-31
Completion date
2016-11-30
Last updated
2016-11-11

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

Conditions

Diabetes, Type 1 Diabetes

Keywords

diabetes, adolescent, young adult, behavioral economics, financial incentives, social incentives

Brief summary

In this study the investigators will compare a novel approach using daily financial incentives and a tiered sponsor network to motivate adolescents and young adults with type 1 diabetes to improve glycemic control.

Detailed description

Participants will be given daily glucose monitoring goals of ≥4 glucose checks per day with ≥1 readings within goal range (70-180 mg/dL) and provided with iHealth wireless glucometers. Half of the study participants will be randomized to the 3-month intervention arm on Way to Health. The intervention includes daily financial incentives ($60 in an account at beginning of each month with $2 daily loss if non-adherent) and a 2-level tiered sponsor network (youth select 2 people who will be notified of non-adherence after 2 and 5 consecutive days). The primary outcome will be HbA1c at 3 months compared to baseline. Secondary outcomes will include HbA1c at 6 months and the proportion of participants adherent to daily glucose monitoring goals. Exit interviews will elicit intervention feasibility and feedback from a youth perspective.

Interventions

BEHAVIORALDaily feedback

Daily feedback on glucose levels from wireless glucometers

BEHAVIORALFinancial incentive

Participant receive a $2 daily financial incentive framed as a loss with money allocated upfront and taken away each day of non-adherence to goal

Sponsors

Children's Hospital of Philadelphia
CollaboratorOTHER
University of Pennsylvania
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
14 Years to 20 Years
Healthy volunteers
Yes

Inclusion criteria

* Diagnosis of type 1 diabetes * HbA1c of 8 or greater * Receiving care from the Childrens Hospital of Philadelphia Diabetes Center * English-speaking * Owns a smartphone

Exclusion criteria

* New diagnosis of type 1 diabetes within past year * Unable to provide informed consent * Already participating in another study to improve glycemic control * Any medical conditions that would prevent completion of the study

Design outcomes

Primary

MeasureTime frameDescription
Change in HbA1c by 3 months3 monthsChange in HbA1c from baseline to 3 months

Secondary

MeasureTime frameDescription
Change in HbA1c by 6 months6 monthsChange in HbA1c from baseline to 6 months
Glucose Monitoring Adherence by 3 months3 monthsProportion of time adherence to glucose monitoring during 3 month intervention
Glucose Monitoring Adherence by 6 months6 monthsProportion of time adherence to glucose monitoring during 3 month follow-up period

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026