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Do Patient-Centric mHealth Programs Improve Patient Engagement and Health Outcomes.

Do Patient-Centric mHealth Programs Improve Patient Engagement and Health Outcomes.

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02757183
Enrollment
20
Registered
2016-05-02
Start date
2016-04-30
Completion date
2017-03-31
Last updated
2016-05-13

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

Conditions

Diabetes

Brief summary

The INTELLIH (brand name of the mobile health application) Diabetes Study is to understand the usage of a mobile health application, IntelliH, and connected wireless devices such as glucometer by the diabetic patients and ascertain if there are any improvements in short-term health outcomes.

Detailed description

The proposed pilot program is the first of its kind in the nation to use a product, IntelliH - Intelligent Health for All, that combines four key technologies in one platform: 1) Mobile health application (mHealth) App and web portal, 2) wireless sensors and wearable devices, 3) Secure text messaging when both sender and receiver are logged in to the system and video-based patient interaction, and 4) remote health monitoring. The purpose of this pilot program is to understand a) usage and adoption of these technologies by providers and patients, and b) document the short-term improvements in health outcomes in a diabetic population. This pilot study will follow 20 diabetic patients (Type 1 or Type 2) as they beta-test this system, and will acquire data on consented subjects over a period of six months.

Interventions

DEVICEIntelliH

IntelliH is a mobile health and a web-based software application that allows patients to enter their blood glucose, weight, medication, diet and other life-style data for review by their providers and monitor their health remotely.

Sponsors

Cedars-Sinai Medical Center
CollaboratorOTHER
AnalyticsPlus, Inc.
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* A1c greater than or equal to 6.5%. * Age greater than or equal to 18 years. * Ability to comply with study protocol. * Available and usable internet facilities at home. * Availability and usable smart phone.

Exclusion criteria

-Inability to comply with instructions and directions.

Design outcomes

Primary

MeasureTime frameDescription
Usage and Adoption of the smart phone based mobile health applicationSix MonthsPatients adoption will be assessed directly through the application and through questionnaire

Secondary

MeasureTime frameDescription
Blood glucose range maintenance and variationSix monthsFrequency of hypoglycemic, hyperglycemic, and out of recommended range events
Adherence to Prescribed MedicationSix monthsMedication adherence rates will be measured for each medication used by patient

Countries

United States

Contacts

Primary ContactRuchi Mathur, MD
Ruchi.mathur@cshs.org(310) 423-4295
Backup ContactLaura Sarmiento, CCRP
Laura.Sarmiento@cshs.org(310) 423-4295

Outcome results

None listed

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