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mHealth Insulin Titration and Management (iSage)

mHealth Insulin Titration and Management (iSage)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03704103
Enrollment
6
Registered
2018-10-12
Start date
2018-08-28
Completion date
2023-08-04
Last updated
2023-08-08

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

Conditions

Type 2 Diabetes Mellitus

Brief summary

The purpose of this study is to determine the benefits of using the iSage app for basal insulin titration and support. By doing this study the investigators hope to learn whether the app improves the participant's ability to follow his/her healthcare provider's instructions to adjust his/her insulin doses.

Interventions

OTHERiSage

The provider will choose a treatment algorithm within the iSage app and set the parameters to make insulin dose adjustments no less frequently than every 7 days. The patient is instructed to perform daily fasting glucose measurements and follow the app's recommendations for insulin adjustment.

Sponsors

University of Kansas Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
21 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Diagnosed Type 2 Diabetes, based on the World Health Organization (WHO) criteria, treated with basal insulin * HbA1c 8-11% inclusive * Glomerular filtration rate (GFR) \> 60 ml/min * Has an Android or iOS based compatible smartphone (iOS 9.0 or above, Android 4.4 or above) * Willing to perform at least 1 fasting finger stick glucose measurements every morning * English speaking

Exclusion criteria

* Diagnosis of hypoglycemic unawareness * Diagnosis of hyperglycemic hyperosmolar non-ketotic coma (HONK) or diabetic ketoacidosis (DKA) within 6 months of enrollment * Recent (within the last 6 months)/current use of non-topical steroids * Insulin requirements in excess of 1 U/kg per day * Use of pioglitazone or another thiazolidinedione (TZD) * In the opinion of the provider, HgbA1c goals should be adjusted above 7% due to infirmity, unstable cardiovascular disease, etc.

Design outcomes

Primary

MeasureTime frameDescription
Concentration of HgbA1c90 daysThe investigators will compare changes in HgbA1c from baseline to day 90.
Number of participants meeting HgbA1c <7%90 daysThe investigators will calculate the percent of patients achieving HgbA1c \<7% at day 90.

Secondary

MeasureTime frameDescription
Sustained use of the iSage app (iSage group only)90 daysThe investigators will compare the percentage of subjects using the app as prescribed versus dropouts.
Hypoglycemia90 daysThe investigators will record the number of episodes of hypoglycemia, to include severity of event, related symptoms, and time of day.

Other

MeasureTime frameDescription
Healthcare resource utilization90 daysNumber of contacts with healthcare resources (including telephone calls), ER visits, clinic visits, hospitalizations
Diabetes Quality of Life Survey (DQOL)90 daysThe investigators will compare DQOL scores from baseline to day 90. The 15-item DQOL Brief Clinical Inventory provides a total health-related quality of life score that predicts self-reported diabetes care behaviors and satisfaction with diabetes control as effectively as the full version of the instrument. Items are scored on a 5-point Likert scale and are of two general formats. One format asks about the frequency of negative impact of diabetes itself or of the diabetes treatment (i.e., How often do you worry about whether you will pass out?) and provides response options from 1 (never) to 5 (all the time). The second format asks about satisfaction with treatment and quality of life (i.e., How satisfied are you with the time you spend exercising?) and is scored from 1 (very satisfied) to 5 (very dissatisfied). Higher scores are negatively valanced, indicating problem frequency or dissatisfaction.
Insulin Treatment Satisfaction Questionnaire (ITSQ)90 daysThe investigators will compare ITSQ scores from baseline to day 90. The 22-item ITSQ is applicable to a wide variety of insulin therapies, and measures insulin treatment satisfaction assessing regimen inconvenience, lifestyle flexibility, glycemic control, hypoglycemic control, and satisfaction with the insulin delivery device. The response scale is ordinal, ranging from 1 (extremely satisfied) to 6 (extremely dissatisfied). The ITSQ is scored among 5 content clusters, forming a total ITSQ score between 0% to 100%, where 100% indicates complete satisfaction with insulin treatment.
iSage Product Satisfaction Survey (iSage group only)90 daysThe investigators will assess iSage app ease of use and satisfaction. Survey consists of 3 items. Answer choices range from 1 (strongly disagree) to 5 (strongly agree).

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026