Clinical trial

Signos DM2 Empowerment Study (SIGNOS-CGM-EMPOWER-201-2022)

Active, not recruiting · Not applicable · 1 countries · Registry ID NCT05874635

Active, not recruitingNot applicableInterventional

What this study is about

The use of continuous glucose monitoring (CGM) in earlier data has inspired behavioral changes leading to improved adherence to an exercise plan in individuals and eating habits in people with diabetes. Mobile health (mHealth) platforms provide satisfactory, easy-to-use tools to help participants in the pursuit of weight change goals. We hypothesize that the use of CGM data and the Signos mHealth platform will assist with weight control in a population of people with type 2 diabetes mellitus who are not using insulin.

A promising-looking record is not the same as confirmed eligibility. The study team must review the full criteria and current recruitment status.

Basic eligibility

Age18 Years to Not listed
SexAll
Healthy volunteersAccepted
ConditionWeight Loss, Metabolic Syndrome, Diabetes Mellitus, Type 2, Central Obesity, Insulin Resistance, Glucose Intolerance, Metabolic Glucose Disorders

Full registry criteria

Inclusion Criteria: * Medical diagnosis of Type 2 Diabetes; determined by review of subject-provided most recent Hg A1c. * Subject is under current care of a primary care provider or specialist * Clearance by medical provider to participate in diet, physical activity, and lifestyle changes * 18 years and above * Own a smartphone and be willing to install the Signos App to personally receive text messages or have access to a web-based survey to self-report their weight. * Willingness to complete quality of life questionnaires or other in-app surveys. * Willingness to use CGM device * Able to speak and read English * Be a Signos mHealth (mobile/web-based) user Exclusion Criteria: * Medical diagnosis of Type 1 Diabetes * Type 2 Diabetes currently using insulin or most recent A1c ≥10% * Severe hypoglycemia \<54 mg/dl resulting in seizure or unconsciousness, or requiring assistance/EMS/hospitalization - within 3 months prior to enrollment * Current medical diagnosis of an eating disorder (such as anorexia nervosa or bulimia) * Medical conditions (e.g., such as seizure disorder) requiring a specific medical diet. * Inborn error of metabolism such as phenylketonuria (PKU), glycogen storage disease, fructose intolerance, Maple Sugar Urine Disease (MSUD). * History of 10 or more soft tissue skin infections (such as cellulitis or abscesses) * Intolerable skin reaction from adhesive * Currently taking any of the following medications: Clozapine, Hydroxyurea, or any form of insulin.

Treatments and study arms

Continuous Glucose Monitor Device

Device

Continuous glucose monitoring automatically tracks blood glucose levels, also called blood sugar, throughout the day and night. You can see your glucose level anytime at a glance. You can also review how your glucose changes over a few hours or days to see trends. Seeing glucose levels in real time can help you make more informed decisions throughout the day about how to balance your food and physical activity.

Primary outcomes

Glucose Metrics via Continuous Glucose Measurement (CGM)During enrollment in the trial for a maximum of 5 years, including a 1 year follow up period, for a maximum of 6 years.

Glucose measured in mg/dl

Change in weight in poundsDuring enrollment in the trial for a maximum of 5 years, including a 1 year follow up period, for a maximum of 6 years.

Change in number of pounds

App engagementDuring enrollment in the trial for a maximum of 5 years, including a 1 year follow up period, for a maximum of 6 years.

Meals logged, Exercises logged, Activities completed

Study locations

1 locations were listed when this page was built. The first 40 are shown.

Signos🇺🇸 Palo Alto, California, United States