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Single arm intervention study of the efficacy of the App for improving the lifestyle behavior in patients with Type 2 DM

Not Applicable
Conditions
Diabetes
Registration Number
JPRN-UMIN000043815
Lead Sponsor
Mitsubishi Tanabe Pharma Corporation
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
58
Inclusion Criteria

Not provided

Exclusion Criteria

1) A female subject who wishes to become pregnant, is pregnant, or is breastfeeding 2) Patients diagnosed with type 1 diabetes mellitus 3) Patients with a diagnosis of secondary diabetes mellitus 4) Patients with physician-determined advanced complications 5) Patients scheduled for hospitalization or surgery during this study 6) Patients with diseases other than diabetes mellitus who are instructed to restrict exercise 7) Patients who have participated in a clinical study or a post-marketing clinical study of another prescription drug or a medical device within 3 months, who are now participating in such a study, or who plan to participate in such a study during this study 8) Patients who have used a mobile application running on a smartphone terminal for the purpose of managing or assisting diabetes mellitus within the past 3 months 9) Medical institution staff or close relatives involved in this study 10) Other patients judged by the investigator to be inappropriate for inclusion in this study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
weight, HbA1c, completion rate, utilization of App, improvement of blood test value
Secondary Outcome Measures
NameTimeMethod
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