Purpose

The purpose of this study is to determine the effectiveness of mobile health applications in improving health outcomes and type II diabetes outcomes in type 2 diabetics. This study will involve a 6-month long commitment where participants will be expected to weigh themselves every morning, at the same time, and check their blood glucose readings daily before and after meals for at least three meals in the day.

Conditions

Eligibility

Eligible Ages
Between 18 Years and 64 Years
Eligible Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Diagnosed with type II diabetes for at least 3 months - Between the age of 18-64 - BMI ≥ 25 - Monitors blood glucose regularly (at least once per day) - Owns or has access to a bathroom weight scale - Owns a smartphone and willing to download mobile app

Exclusion Criteria

  • Does not check blood glucose at least once per day - On medications that promote weight gain such as antipsychotic, antidepressant, and steroid hormone medications. Medications for diabetes such as insulin, thiazolidinediones or sulfonylureas are oka

Study Design

Phase
N/A
Study Type
Interventional
Allocation
Randomized
Intervention Model
Factorial Assignment
Primary Purpose
Treatment
Masking
Single (Participant)

Arm Groups

ArmDescriptionAssigned Intervention
No Intervention
Control
Experimental
Healthi
  • Other: Mobile health application
    Intervention will be with mobile health application

Recruiting Locations

San Diego State University
San Diego 5391811, California 5332921 92182
Contact:
Mee Young Hong, PhD
619-594-2392
mhong2@sdsu.edu

More Details

Status
Recruiting
Sponsor
San Diego State University

Study Contact

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.